geneid | 10673 |
---|---|
ensemblid | ENSG00000102524.12 |
hgncid | 11929 |
symbol | TNFSF13B |
name | TNF superfamily member 13b |
refseq_nuc | NM_006573.5 |
refseq_prot | NP_006564.1 |
ensembl_nuc | ENST00000375887.9 |
ensembl_prot | ENSP00000365048.3 |
mane_status | MANE Select |
chr | chr13 |
start | 108269718 |
end | 108308478 |
strand | + |
ver | v1.2 |
region | chr13:108269718-108308478 |
region5000 | chr13:108264718-108313478 |
regionname0 | TNFSF13B_chr13_108269718_108308478 |
regionname5000 | TNFSF13B_chr13_108264718_108313478 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 285 | 383 | 90 | 77 | 160 | 18 | 36 | 118 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0002 | 0/0 | 285 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 858 | 380 | 87 | 77 | 160 | 18 | 36 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
c0002 | 0/0 | 858 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
c0003 | 0/0 | 858 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1715 | 54 | 26 | 16 | 2 | 4 | 6 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0002 | 1/1 | 1719 | 48 | 10 | 10 | 12 | 6 | 8 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0003 | 0/0 | 1706 | 45 | 0 | 6 | 35 | 1 | 3 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0004 | 0/0 | 1716 | 44 | 0 | 1 | 41 | 0 | 2 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0005 | 0/0 | 1717 | 38 | 1 | 10 | 24 | 2 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0006 | 0/0 | 1714 | 37 | 27 | 8 | 1 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0007 | 0/0 | 1716 | 29 | 2 | 5 | 21 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0008 | 0/0 | 1720 | 22 | 2 | 5 | 7 | 1 | 7 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0009 | 0/0 | 1718 | 11 | 2 | 2 | 7 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0010 | 0/0 | 1718 | 7 | 0 | 2 | 2 | 1 | 2 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0011 | 0/0 | 1718 | 6 | 0 | 5 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0012 | 0/0 | 1716 | 5 | 3 | 1 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0013 | 0/0 | 1708 | 5 | 5 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0014 | 0/0 | 1715 | 4 | 0 | 0 | 3 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0015 | 0/0 | 1717 | 3 | 1 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0016 | 0/0 | 1717 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0017 | 0/0 | 1719 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0018 | 0/0 | 1719 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0019 | 0/0 | 1714 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0020 | 0/0 | 1710 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0021 | 0/0 | 1712 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0022 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0023 | 0/0 | 1719 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0024 | 0/0 | 1719 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0025 | 0/0 | 1717 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0026 | 0/0 | 1717 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0027 | 0/0 | 1717 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0028 | 0/0 | 1717 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0029 | 0/0 | 1717 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0030 | 0/0 | 1716 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0031 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0032 | 0/0 | 1715 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0033 | 0/0 | 1714 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0034 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
t0035 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 858 | 380 | 87 | 77 | 160 | 18 | 36 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0002 | 0/0 | 858 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0002c0003 | 0/0 | 858 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2572 | 54 | 26 | 16 | 2 | 4 | 6 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0002 | 1/1 | 2576 | 46 | 9 | 9 | 12 | 6 | 8 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0003 | 0/0 | 2563 | 45 | 0 | 6 | 35 | 1 | 3 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0004 | 0/0 | 2573 | 44 | 0 | 1 | 41 | 0 | 2 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0005 | 0/0 | 2574 | 38 | 1 | 10 | 24 | 2 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0006 | 0/0 | 2571 | 37 | 27 | 8 | 1 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0007 | 0/0 | 2573 | 29 | 2 | 5 | 21 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0008 | 0/0 | 2577 | 22 | 2 | 5 | 7 | 1 | 7 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0009 | 0/0 | 2575 | 11 | 2 | 2 | 7 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0010 | 0/0 | 2575 | 7 | 0 | 2 | 2 | 1 | 2 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0011 | 0/0 | 2575 | 6 | 0 | 5 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0012 | 0/0 | 2573 | 5 | 3 | 1 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0013 | 0/0 | 2565 | 5 | 5 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0014 | 0/0 | 2572 | 4 | 0 | 0 | 3 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0015 | 0/0 | 2574 | 3 | 1 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0016 | 0/0 | 2574 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0017 | 0/0 | 2576 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0018 | 0/0 | 2576 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0019 | 0/0 | 2571 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0020 | 0/0 | 2567 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0022 | 0/0 | 2577 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0023 | 0/0 | 2576 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0024 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0025 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0026 | 0/0 | 2574 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0027 | 0/0 | 2574 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0028 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0029 | 0/0 | 2574 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0030 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0031 | 0/0 | 2572 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0032 | 0/0 | 2572 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0033 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0034 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0001t0035 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0002t0002 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0001c0002t0021 | 0/0 | 2569 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
a0002c0003t0002 | 0/0 | 2576 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | copy fasta | chr13 | 108264718 | 108313478 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0006g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0007g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0008g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0009g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0010g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0011g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0011g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0011g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0011g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0012g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0012g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0013g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0014g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0014g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0014g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0015g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0015g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0015g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0017g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0017g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0018g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0018g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0019g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0019g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0020g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0020g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0023g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0024g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0025g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0026g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0027g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0028g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0029g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0030g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0031g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0032g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0033g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0034g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0001t0035g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0002t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0001c0002t0021g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0033 | g0144 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0277 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0198 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0102 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0318 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00280 | hp2 | a0001 | c0001 | t0008 | g0236 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0218 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00408 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00408 | hp2 | a0001 | c0001 | t0005 | g0336 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00597 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00621 | hp1 | a0001 | c0001 | t0005 | g0310 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00639 | hp1 | a0001 | c0001 | t0017 | g0315 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0158 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0332 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG00741 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01069 | hp1 | a0001 | c0001 | t0011 | g0016 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0333 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0019 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01071 | hp1 | a0001 | c0001 | t0011 | g0016 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0019 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01074 | hp2 | a0001 | c0001 | t0009 | g0294 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0072 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0331 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01168 | hp1 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01168 | hp2 | a0001 | c0001 | t0009 | g0313 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01169 | hp1 | a0001 | c0001 | t0018 | g0314 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01175 | hp2 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01192 | hp1 | a0001 | c0001 | t0029 | g0289 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0170 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0276 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0303 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0319 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01256 | hp2 | a0001 | c0001 | t0026 | g0020 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01258 | hp1 | a0001 | c0001 | t0011 | g0020 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01261 | hp2 | a0001 | c0001 | t0032 | g0290 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0330 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0043 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0344 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01884 | hp1 | a0001 | c0001 | t0016 | g0209 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01928 | hp1 | a0001 | c0001 | t0007 | g0100 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01934 | hp1 | a0002 | c0003 | t0002 | g0066 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0095 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0279 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01952 | hp1 | a0001 | c0001 | t0012 | g0316 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0185 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0093 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0320 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0350 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01981 | hp2 | a0001 | c0001 | t0017 | g0015 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01993 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02004 | hp2 | a0001 | c0001 | t0007 | g0099 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02015 | hp2 | a0001 | c0001 | t0025 | g0047 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0271 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0201 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0352 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0244 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0114 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0127 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02132 | hp1 | a0001 | c0001 | t0007 | g0178 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02148 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02155 | hp1 | a0001 | c0001 | t0015 | g0233 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0257 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0085 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0340 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02647 | hp1 | a0001 | c0001 | t0028 | g0156 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0204 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02698 | hp2 | a0001 | c0001 | t0034 | g0239 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02717 | hp1 | a0001 | c0002 | t0021 | g0325 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0214 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0184 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02970 | hp1 | a0001 | c0001 | t0013 | g0122 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02970 | hp2 | a0001 | c0001 | t0020 | g0141 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0243 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0182 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03195 | hp1 | a0001 | c0002 | t0021 | g0229 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03195 | hp2 | a0001 | c0001 | t0031 | g0221 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03225 | hp1 | a0001 | c0001 | t0015 | g0311 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03225 | hp2 | a0001 | c0001 | t0019 | g0113 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03239 | hp1 | a0001 | c0001 | t0027 | g0301 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03239 | hp2 | a0001 | c0001 | t0008 | g0282 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03486 | hp1 | a0001 | c0001 | t0013 | g0187 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03486 | hp2 | a0001 | c0001 | t0012 | g0087 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0207 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03654 | hp2 | a0001 | c0001 | t0007 | g0021 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0106 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0347 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03688 | hp2 | a0001 | c0001 | t0008 | g0155 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03704 | hp1 | a0001 | c0001 | t0014 | g0052 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03704 | hp2 | a0001 | c0001 | t0008 | g0045 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03831 | hp1 | a0001 | c0001 | t0023 | g0107 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0291 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03927 | hp1 | a0001 | c0001 | t0030 | g0195 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03942 | hp1 | a0001 | c0001 | t0008 | g0283 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04115 | hp1 | a0001 | c0001 | t0008 | g0211 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0042 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04184 | hp1 | a0001 | c0001 | t0008 | g0247 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04184 | hp2 | a0001 | c0001 | t0012 | g0222 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04204 | hp2 | a0001 | c0001 | t0010 | g0104 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18939 | hp1 | a0001 | c0001 | t0022 | g0089 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18939 | hp2 | a0001 | c0001 | t0008 | g0067 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18942 | hp1 | a0001 | c0001 | t0014 | g0123 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18951 | hp1 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18953 | hp1 | a0001 | c0001 | t0007 | g0258 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0272 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0346 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0356 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18962 | hp1 | a0001 | c0001 | t0014 | g0081 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18963 | hp1 | a0001 | c0001 | t0007 | g0274 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18964 | hp1 | a0001 | c0001 | t0009 | g0183 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18964 | hp2 | a0001 | c0001 | t0035 | g0307 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18965 | hp1 | a0001 | c0001 | t0008 | g0273 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18974 | hp2 | a0001 | c0001 | t0009 | g0327 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18977 | hp1 | a0001 | c0001 | t0009 | g0245 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0349 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18980 | hp2 | a0001 | c0001 | t0010 | g0235 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0260 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18989 | hp2 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18990 | hp2 | a0001 | c0001 | t0009 | g0261 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18993 | hp2 | a0001 | c0001 | t0007 | g0231 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18997 | hp1 | a0001 | c0001 | t0008 | g0190 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18997 | hp2 | a0001 | c0001 | t0009 | g0193 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19004 | hp1 | a0001 | c0001 | t0014 | g0353 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19004 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19005 | hp1 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0351 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19043 | hp2 | a0001 | c0001 | t0019 | g0213 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19059 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0172 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19068 | hp1 | a0001 | c0001 | t0008 | g0073 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19070 | hp1 | a0001 | c0001 | t0007 | g0119 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19079 | hp2 | a0001 | c0001 | t0008 | g0339 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19080 | hp2 | a0001 | c0001 | t0015 | g0046 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19081 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19081 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0132 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0250 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ASW | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ASW | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20752 | hp1 | a0001 | c0001 | t0010 | g0149 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20752 | hp2 | a0001 | c0001 | t0011 | g0302 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | GIH | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0255 | SAS | GIH | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0094 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0208 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0179 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0275 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03471 | hp1 | a0001 | c0001 | t0024 | g0232 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG06807 | hp1 | a0001 | c0001 | t0013 | g0074 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0308 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA20300 | hp2 | a0001 | c0001 | t0020 | g0286 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0292 | REF | REF | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0055 | REF | REF | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:108270208
|
G | A | 1 | a0002 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.313G>A | p.Ala105Thr | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 1/6 | 491/2576 | 313/858 | 105/285 | chr13 | 108270208 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:108303585
|
T | C | 1 | a0001c0002 | 3 | HG02280.hp1 HG02717.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.726T>C | p.Asn242Asn | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/6 | 904/2576 | 726/858 | 242/285 | chr13 | 108303585 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:108269850
|
G | T | 1 | a0001c0001t0035 | 1 | NA18964.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 1/6 | chr13 | 108269850 | ||||||
chr13:108307016
|
C | CA | 2 | a0001c0001t0008a0001c0001t0022 | 23 | HG00280.hp2 HG00738.hp1 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*109dupA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 110 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CA | C | 3 | a0001c0001t0009a0001c0001t0010a0001c0001t0011 | 24 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*109delA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 109 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CAA | C | 6 | a0001c0001t0005a0001c0001t0025a0001c0001t0026others(3): Show | 43 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*108_*109delAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 108 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CAAA | C | 5 | a0001c0001t0004a0001c0001t0012a0001c0001t0015others(2): Show | 54 | HG00423.hp2 HG00544.hp2 HG01255.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*107_*109delAAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 107 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CAAAA | C | 5 | a0001c0001t0001a0001c0001t0007a0001c0001t0014others(2): Show | 89 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*109delAAAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 106 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CAAAAA | C | 3 | a0001c0001t0006a0001c0001t0019a0001c0001t0033 | 40 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*105_*109delAAAAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 105 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CAAAAAAA | C | 3 | a0001c0001t0013a0001c0001t0020a0001c0002t0021 | 9 | HG02717.hp1 HG02970.hp1 HG02970.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*103_*109delAAAAAA others(1): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 103 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0034 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98_*109delAAAAAAA others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 98 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307016
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003 | 45 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*97_*109delAAAAAAA others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 97 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | ||||
chr13:108307102
|
C | T | 1 | a0001c0001t0029 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 164 | chr13 | 108307102 | |||||
chr13:108307259
|
C | A | 1 | a0001c0001t0025 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 321 | chr13 | 108307259 | |||||
chr13:108307523
|
C | T | 1 | a0001c0001t0019 | 2 | HG03225.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*585C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 585 | chr13 | 108307523 | |||||
chr13:108307597
|
A | AT | 2 | a0001c0001t0007a0001c0001t0015 | 32 | HG00408.hp1 HG00597.hp1 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*666dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 667 | INFO_REALIGN_3_PRIME | chr13 | 108307597 | ||||
chr13:108307609
|
GGA | G | 3 | a0001c0001t0013a0001c0001t0016a0001c0001t0020 | 9 | HG01884.hp1 HG02055.hp2 HG02970.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*680_*681delGA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 680 | INFO_REALIGN_3_PRIME | chr13 | 108307609 | ||||
chr13:108307641
|
C | T | 1 | a0001c0001t0030 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 703 | chr13 | 108307641 | |||||
chr13:108307709
|
G | A | 3 | a0001c0001t0011a0001c0001t0017a0001c0001t0026 | 9 | HG00639.hp1 HG00741.hp2 HG01069.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*771G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 771 | chr13 | 108307709 | |||||
chr13:108307840
|
T | A | 14 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(11): Show | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*902T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 902 | chr13 | 108307840 | |||||
chr13:108308037
|
T | A | 1 | a0001c0001t0027 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1099 | chr13 | 108308037 | |||||
chr13:108308067
|
C | T | 1 | a0001c0001t0018 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1129C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1129 | chr13 | 108308067 | |||||
chr13:108308102
|
GTT | G | 1 | a0001c0001t0013 | 5 | HG02970.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1166_*1167delTT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1166 | INFO_REALIGN_3_PRIME | chr13 | 108308102 | ||||
chr13:108308379
|
G | A | 2 | a0001c0001t0024a0001c0001t0031 | 2 | HG03195.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1441G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1441 | chr13 | 108308379 | |||||
chr13:108308401
|
G | A | 1 | a0001c0001t0019 | 2 | HG03225.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1463G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1463 | chr13 | 108308401 | |||||
chr13:108308473
|
C | T | 2 | a0001c0001t0032a0001c0001t0033 | 2 | HG00099.hp1 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1535 | chr13 | 108308473 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:108270295
|
C | G | 37 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0001g0341others(34): Show | 39 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.340-45C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 1/5 | chr13 | 108270295 | ||||||
chr13:108270749
|
A | G | 13 | a0001c0001t0001g0322a0001c0001t0002g0317a0001c0001t0002g0321others(10): Show | 14 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.424+325A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108270749 | ||||||
chr13:108270893
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+469A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108270893 | ||||||
chr13:108270931
|
T | C | 1 | a0001c0001t0007g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.424+507T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108270931 | ||||||
chr13:108270950
|
T | TAC | 19 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0322others(16): Show | 22 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+545_424+546dup others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | |||||
chr13:108270950
|
T | TACACACA others(1): Show |
29 | a0001c0001t0001g0341a0001c0001t0002g0335a0001c0001t0002g0342others(26): Show | 31 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.424+539_424+546dup others(8): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | |||||
chr13:108270950
|
T | TACACACA others(3): Show |
3 | a0001c0001t0004g0328a0001c0001t0004g0329a0001c0001t0009g0327 | 3 | NA18974.hp2 NA18993.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.424+537_424+546dup others(10): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | |||||
chr13:108270950
|
T | TACACACA others(5): Show |
1 | a0001c0001t0001g0326 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+535_424+546dup others(12): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | |||||
chr13:108270950
|
T | TACACACA others(7): Show |
2 | a0001c0001t0002g0324a0001c0002t0021g0325 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.424+533_424+546dup others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | |||||
chr13:108270950
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0323 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.424+531_424+546dup others(16): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | |||||
chr13:108271101
|
G | T | 2 | a0001c0001t0001g0322a0001c0001t0002g0321 | 2 | HG01167.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.424+677G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271101 | ||||||
chr13:108271379
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+955A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271379 | ||||||
chr13:108271429
|
C | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0025 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424+1005C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271429 | ||||||
chr13:108271444
|
T | TCA | 20 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0002g0025others(17): Show | 21 | HG00423.hp1 HG01496.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+1064_424+1065d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
T | TCACA | 10 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0002g0026others(7): Show | 10 | HG00642.hp2 HG00741.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+1062_424+1065d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCA | T | 52 | a0001c0001t0001g0112a0001c0001t0001g0140a0001c0001t0001g0143others(49): Show | 55 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.424+1064_424+1065d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACA | T | 67 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0168others(64): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.424+1062_424+1065d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACACA | T | 96 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0227others(93): Show | 104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.424+1060_424+1065d others(8): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACACAC others(1): Show |
T | 47 | a0001c0001t0001g0018a0001c0001t0001g0295a0001c0001t0001g0296others(44): Show | 53 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.424+1058_424+1065d others(10): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACACAC others(3): Show |
T | 5 | a0001c0001t0001g0305a0001c0001t0002g0304a0001c0001t0002g0306others(2): Show | 5 | HG01261.hp1 HG02148.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+1056_424+1065d others(12): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACACAC others(5): Show |
T | 2 | a0001c0001t0004g0357a0001c0001t0006g0308 | 2 | NA18963.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.424+1054_424+1065d others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACACAC others(7): Show |
T | 4 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0324others(1): Show | 4 | HG02717.hp1 HG03139.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+1052_424+1065d others(16): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACACAC others(9): Show |
T | 2 | a0001c0001t0005g0309a0001c0001t0005g0310 | 2 | HG00621.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.424+1050_424+1065d others(18): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271444
|
TCACACAC others(13): Show |
T | 1 | a0001c0001t0015g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424+1046_424+1065d others(22): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | |||||
chr13:108271480
|
A | T | 1 | a0001c0001t0001g0018 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.424+1056A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271480 | ||||||
chr13:108271512
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+1088A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271512 | ||||||
chr13:108271570
|
A | G | 37 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0001g0341others(34): Show | 39 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.424+1146A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271570 | ||||||
chr13:108271586
|
G | A | 1 | a0001c0001t0004g0223 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.424+1162G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271586 | ||||||
chr13:108271610
|
A | G | 3 | a0001c0001t0004g0108a0001c0001t0007g0159a0001c0001t0012g0222 | 3 | HG04184.hp2 NA18747.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.424+1186A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271610 | ||||||
chr13:108271692
|
G | A | 36 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0001g0341others(33): Show | 38 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.424+1268G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271692 | ||||||
chr13:108271737
|
C | T | 3 | a0001c0001t0005g0106a0001c0001t0023g0107a0001c0001t0031g0221 | 3 | HG03195.hp2 HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.424+1313C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271737 | ||||||
chr13:108271931
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.424+1507T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271931 | ||||||
chr13:108272006
|
T | C | 3 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0161 | 3 | NA18998.hp1 NA19059.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.424+1582T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272006 | ||||||
chr13:108272233
|
C | T | 1 | a0001c0001t0004g0287 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.424+1809C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272233 | ||||||
chr13:108272404
|
T | C | 3 | a0001c0001t0003g0110a0001c0001t0004g0109a0001c0001t0005g0111 | 3 | NA18948.hp1 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.424+1980T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272404 | ||||||
chr13:108272566
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.424+2142T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272566 | ||||||
chr13:108272812
|
C | G | 1 | a0001c0001t0020g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.424+2388C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272812 | ||||||
chr13:108272859
|
TA | T | 5 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0324others(2): Show | 5 | HG02717.hp1 HG03139.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2444delA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108272859 | |||||
chr13:108273215
|
T | A | 9 | a0001c0001t0001g0165a0001c0001t0001g0227a0001c0001t0002g0162others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2791T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273215 | ||||||
chr13:108273485
|
G | GAAATGGA others(40): Show |
1 | a0001c0001t0009g0327 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.424+3064_424+3110d others(49): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108273485 | |||||
chr13:108273486
|
A | G | 1 | a0001c0002t0021g0325 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424+3062A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273486 | ||||||
chr13:108273549
|
T | C | 1 | a0001c0001t0006g0166 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.424+3125T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273549 | ||||||
chr13:108273755
|
C | A | 1 | a0001c0001t0003g0167 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.424+3331C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273755 | ||||||
chr13:108273932
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+3508C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273932 | ||||||
chr13:108274047
|
A | T | 212 | a0001c0001t0001g0018a0001c0001t0001g0092a0001c0001t0001g0096others(209): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.424+3623A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274047 | ||||||
chr13:108274122
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+3698G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274122 | ||||||
chr13:108274139
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0013g0091 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+3715G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274139 | ||||||
chr13:108274267
|
G | C | 8 | a0001c0001t0001g0165a0001c0001t0001g0227a0001c0001t0002g0162others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+3843G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274267 | ||||||
chr13:108274278
|
TATACATA others(6): Show |
T | 2 | a0001c0001t0007g0011a0001c0001t0015g0233 | 3 | HG00597.hp1 HG02155.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.424+3876_424+3888d others(15): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274278 | |||||
chr13:108274283
|
A | T | 1 | a0001c0001t0002g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+3859A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274283 | ||||||
chr13:108274290
|
C | CAATACAT others(22): Show |
5 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0150others(2): Show | 5 | HG00639.hp2 HG01081.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+3878_424+3879i others(31): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274290 | |||||
chr13:108274366
|
AAT | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(223): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.424+3956_424+3957d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274366 | |||||
chr13:108274366
|
AATAT | A | 13 | a0001c0001t0001g0165a0001c0001t0001g0227a0001c0001t0001g0323others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+3954_424+3957d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274366 | |||||
chr13:108274549
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+4125G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274549 | ||||||
chr13:108274641
|
T | C | 32 | a0001c0001t0001g0341a0001c0001t0002g0335a0001c0001t0002g0342others(29): Show | 34 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+4217T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274641 | ||||||
chr13:108274731
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.424+4307C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274731 | ||||||
chr13:108275155
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0322others(17): Show | 23 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+4731G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275155 | ||||||
chr13:108275361
|
C | G | 1 | a0001c0001t0002g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+4937C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275361 | ||||||
chr13:108275366
|
A | C | 1 | a0001c0001t0002g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+4942A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275366 | ||||||
chr13:108275401
|
T | C | 4 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0324others(1): Show | 4 | HG02717.hp1 HG03139.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4977T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275401 | ||||||
chr13:108275404
|
T | A | 1 | a0001c0001t0002g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+4980T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275404 | ||||||
chr13:108275457
|
C | A | 1 | a0001c0001t0004g0040 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.424+5033C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275457 | ||||||
chr13:108275507
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+5083T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275507 | ||||||
chr13:108275518
|
A | C | 1 | a0001c0001t0002g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+5094A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275518 | ||||||
chr13:108275550
|
A | C | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+5126A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275550 | ||||||
chr13:108275580
|
G | A | 1 | a0001c0001t0013g0091 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.424+5156G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275580 | ||||||
chr13:108275836
|
G | A | 1 | a0001c0001t0005g0234 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.424+5412G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275836 | ||||||
chr13:108275897
|
AT | A | 3 | a0001c0001t0002g0146a0001c0001t0009g0327a0001c0001t0010g0235 | 3 | NA18974.hp2 NA18980.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.424+5479delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108275897 | |||||
chr13:108275947
|
T | C | 1 | a0001c0001t0007g0114 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.424+5523T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275947 | ||||||
chr13:108275967
|
A | G | 1 | a0001c0001t0008g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.424+5543A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275967 | ||||||
chr13:108275992
|
G | A | 10 | a0001c0001t0001g0165a0001c0001t0001g0227a0001c0001t0001g0228others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+5568G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275992 | ||||||
chr13:108276145
|
G | A | 1 | a0001c0001t0013g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.424+5721G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276145 | ||||||
chr13:108276155
|
C | T | 1 | a0001c0001t0035g0307 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.424+5731C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276155 | ||||||
chr13:108276388
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.424+5964A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276388 | ||||||
chr13:108276420
|
T | A | 1 | a0001c0001t0003g0167 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.424+5996T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276420 | ||||||
chr13:108276502
|
G | C | 88 | a0001c0001t0001g0160a0001c0001t0001g0191a0001c0001t0001g0192others(85): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.424+6078G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276502 | ||||||
chr13:108276531
|
G | A | 1 | a0001c0001t0008g0236 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.424+6107G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276531 | ||||||
chr13:108276590
|
C | CA | 23 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0196others(20): Show | 27 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.424+6173dupA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108276590 | |||||
chr13:108276691
|
T | A | 1 | a0001c0001t0004g0334 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.424+6267T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276691 | ||||||
chr13:108276718
|
C | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0196others(21): Show | 28 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+6294C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276718 | ||||||
chr13:108276766
|
A | AT | 13 | a0001c0001t0001g0165a0001c0001t0001g0227a0001c0001t0001g0228others(10): Show | 13 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+6350dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108276766 | |||||
chr13:108277069
|
TACAGAGA others(5): Show |
T | 1 | a0001c0001t0010g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.424+6650_424+6661d others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108277069 | |||||
chr13:108277207
|
G | C | 1 | a0001c0001t0015g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.424+6783G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108277207 | ||||||
chr13:108277315
|
C | T | 244 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(241): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.424+6891C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108277315 | ||||||
chr13:108277926
|
A | G | 1 | a0001c0001t0030g0195 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.424+7502A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108277926 | ||||||
chr13:108278540
|
T | G | 4 | a0001c0001t0001g0196a0001c0001t0006g0054a0001c0001t0006g0308others(1): Show | 4 | HG02258.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+8116T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278540 | ||||||
chr13:108278572
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0001t0033g0144 | 3 | HG00099.hp1 HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.424+8148C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278572 | ||||||
chr13:108278578
|
C | CTCCTCCT others(270): Show |
1 | a0001c0001t0003g0167 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(279): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(445): Show |
1 | a0001c0001t0003g0036 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(454): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(779): Show |
1 | a0001c0001t0007g0172 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(788): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(781): Show |
1 | a0001c0001t0006g0056 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(790): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(694): Show |
1 | a0001c0001t0003g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(703): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(627): Show |
1 | a0001c0001t0005g0093 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(636): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(614): Show |
1 | a0001c0001t0003g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(669): Show |
1 | a0001c0001t0009g0294 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(678): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(270): Show |
1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(279): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(626): Show |
1 | a0001c0001t0024g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(445): Show |
1 | a0001c0001t0003g0037 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(454): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(591): Show |
1 | a0001c0001t0003g0237 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(600): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(690): Show |
1 | a0001c0001t0007g0043 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(699): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(646): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0026 | 3 | HG00642.hp2 HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(655): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(631): Show |
2 | a0001c0001t0001g0092a0001c0001t0013g0091 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(640): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(613): Show |
2 | a0001c0001t0006g0279a0001c0001t0006g0280 | 2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(622): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(634): Show |
2 | a0001c0001t0002g0238a0001c0001t0034g0239 | 2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(643): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(657): Show |
2 | a0001c0001t0001g0295a0001c0001t0002g0240 | 2 | HG01993.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(666): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(777): Show |
1 | a0001c0001t0004g0059 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(786): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(777): Show |
1 | a0001c0001t0004g0044 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(786): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(776): Show |
30 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0173others(27): Show | 31 | HG00423.hp2 HG00597.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(785): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(614): Show |
1 | a0001c0001t0008g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(591): Show |
1 | a0001c0001t0008g0019 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(600): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(630): Show |
1 | a0001c0001t0004g0242 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(639): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
136 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0096others(133): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(631): Show |
1 | a0001c0001t0004g0189 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(640): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(686): Show |
1 | a0001c0001t0025g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(695): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(708): Show |
1 | a0001c0001t0002g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(717): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(669): Show |
17 | a0001c0001t0001g0031a0001c0001t0001g0051a0001c0001t0001g0086others(14): Show | 17 | HG01192.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(678): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(689): Show |
27 | a0001c0001t0001g0030a0001c0001t0001g0050a0001c0001t0002g0028others(24): Show | 30 | HG00408.hp1 HG00621.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(698): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(724): Show |
1 | a0001c0001t0007g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(733): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(885): Show |
1 | a0001c0001t0005g0033 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(894): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(648): Show |
2 | a0001c0001t0001g0196a0001c0001t0031g0221 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(657): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(626): Show |
1 | a0001c0001t0002g0285 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(684): Show |
4 | a0001c0001t0001g0181a0001c0001t0001g0312a0001c0001t0006g0180others(1): Show | 4 | HG03130.hp1 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(693): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(663): Show |
1 | a0001c0001t0001g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(672): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
1 | a0001c0001t0013g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(619): Show |
1 | a0001c0001t0014g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(628): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(614): Show |
2 | a0001c0001t0003g0010a0001c0001t0008g0185 | 3 | HG01361.hp2 HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(634): Show |
23 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0124others(20): Show | 24 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(643): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(615): Show |
1 | a0001c0001t0005g0330 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(624): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
1 | a0001c0001t0002g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(720): Show |
2 | a0001c0001t0002g0345a0001c0001t0003g0344 | 2 | HG01496.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(729): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(638): Show |
1 | a0001c0001t0004g0223 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(647): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(614): Show |
19 | a0001c0001t0001g0143a0001c0001t0002g0145a0001c0001t0002g0355others(16): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(634): Show |
4 | a0001c0001t0003g0293a0001c0001t0004g0329a0001c0001t0005g0346others(1): Show | 4 | NA18957.hp2 NA18965.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(643): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(613): Show |
1 | a0001c0001t0009g0327 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(622): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
1 | a0001c0001t0001g0006 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(609): Show |
1 | a0001c0001t0007g0274 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(618): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(610): Show |
1 | a0001c0001t0006g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(619): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(689): Show |
1 | a0001c0001t0007g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(698): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
1 | a0001c0001t0008g0275 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(614): Show |
7 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0002g0200others(4): Show | 7 | HG01109.hp2 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(630): Show |
2 | a0001c0001t0006g0210a0001c0001t0008g0211 | 2 | HG01099.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(639): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
14 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0002g0150others(11): Show | 14 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(684): Show |
1 | a0001c0001t0006g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(693): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(633): Show |
1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(642): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(631): Show |
1 | a0001c0001t0005g0277 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(640): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(799): Show |
1 | a0001c0001t0001g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(808): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(772): Show |
1 | a0001c0001t0022g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(781): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(630): Show |
1 | a0001c0001t0006g0308 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(639): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(645): Show |
7 | a0001c0001t0001g0227a0001c0001t0002g0162a0001c0001t0006g0164others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(654): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(662): Show |
1 | a0001c0001t0001g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(671): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(608): Show |
1 | a0001c0001t0001g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(617): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
1 | a0001c0001t0006g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278578
|
C | CTCCTCCT others(611): Show |
1 | a0001c0001t0020g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | |||||
chr13:108278580
|
C | CCTCCTCC others(614): Show |
1 | a0001c0001t0006g0054 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278580 | |||||
chr13:108278587
|
C | CTCTTCCT others(614): Show |
5 | a0001c0001t0001g0206a0001c0001t0009g0207a0001c0001t0009g0208others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278587 | |||||
chr13:108278588
|
T | TCTTCCTC others(612): Show |
1 | a0001c0001t0001g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(621): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278588 | |||||
chr13:108278590
|
C | T | 1 | a0001c0001t0006g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424+8166C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278590 | ||||||
chr13:108278623
|
C | T | 4 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0053others(1): Show | 4 | HG00423.hp1 NA18998.hp1 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-8180C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278623 | ||||||
chr13:108278632
|
T | C | 2 | a0001c0001t0001g0358a0001c0001t0003g0167 | 2 | HG02630.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.425-8171T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278632 | ||||||
chr13:108278646
|
A | C | 1 | a0001c0001t0006g0054 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-8157A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278646 | ||||||
chr13:108278646
|
A | G | 2 | a0001c0001t0001g0358a0001c0001t0003g0167 | 2 | HG02630.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.425-8157A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278646 | ||||||
chr13:108278655
|
T | C | 1 | a0001c0001t0006g0054 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-8148T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278655 | ||||||
chr13:108278658
|
C | CCTCCTCC others(1): Show |
13 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0206others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-8128_425-8121d others(10): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278658 | |||||
chr13:108278658
|
C | CCTCCTCC others(383): Show |
1 | a0001c0001t0003g0167 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.425-8136_425-8135i others(392): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278658 | |||||
chr13:108278666
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.425-8137T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278666 | ||||||
chr13:108278666
|
T | TCCCCTCC others(200): Show |
1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8136_425-8135i others(209): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278666 | |||||
chr13:108278683
|
T | C | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8120T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278683 | ||||||
chr13:108278696
|
T | C | 1 | a0001c0001t0007g0274 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.425-8107T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278696 | ||||||
chr13:108278719
|
T | C | 1 | a0001c0001t0022g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-8084T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278719 | ||||||
chr13:108278720
|
C | T | 1 | a0001c0001t0022g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-8083C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278720 | ||||||
chr13:108278726
|
C | CCCCTTCT others(129): Show |
1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8076_425-8075i others(138): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278726 | |||||
chr13:108278728
|
T | C | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8075T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278728 | ||||||
chr13:108278885
|
T | G | 1 | a0001c0001t0003g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.425-7918T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278885 | ||||||
chr13:108278896
|
G | A | 3 | a0001c0001t0002g0124a0001c0001t0003g0125a0001c0001t0005g0126 | 3 | HG00609.hp1 HG02056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.425-7907G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278896 | ||||||
chr13:108279026
|
T | G | 1 | a0001c0001t0003g0115 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.425-7777T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279026 | ||||||
chr13:108279068
|
A | ATTTGTT | 28 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0124others(25): Show | 30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7735_425-7734i others(8): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279068 | ||||||
chr13:108279069
|
C | A | 28 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0124others(25): Show | 30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7734C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279069 | ||||||
chr13:108279069
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-7734C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279069 | ||||||
chr13:108279070
|
C | G | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-7733C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279070 | ||||||
chr13:108279070
|
C | T | 28 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0124others(25): Show | 30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7733C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279070 | ||||||
chr13:108279071
|
C | G | 28 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0124others(25): Show | 30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7732C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279071 | ||||||
chr13:108279071
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-7732C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279071 | ||||||
chr13:108279072
|
C | T | 29 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0124others(26): Show | 31 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.425-7731C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279072 | ||||||
chr13:108279074
|
T | C | 17 | a0001c0001t0001g0165a0001c0001t0001g0181a0001c0001t0001g0227others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.425-7729T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279074 | ||||||
chr13:108279199
|
G | A | 1 | a0001c0001t0006g0279 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.425-7604G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279199 | ||||||
chr13:108279210
|
T | A | 2 | a0001c0001t0006g0279a0001c0001t0006g0280 | 2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.425-7593T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279210 | ||||||
chr13:108279215
|
C | G | 1 | a0001c0001t0001g0358 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-7588C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279215 | ||||||
chr13:108279224
|
A | T | 1 | a0001c0001t0003g0078 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.425-7579A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279224 | ||||||
chr13:108279255
|
C | T | 1 | a0001c0001t0013g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-7548C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279255 | ||||||
chr13:108279324
|
G | A | 1 | a0001c0001t0010g0094 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.425-7479G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279324 | ||||||
chr13:108279462
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-7341G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279462 | ||||||
chr13:108279463
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-7340A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279463 | ||||||
chr13:108279631
|
T | A | 1 | a0001c0001t0006g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.425-7172T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279631 | ||||||
chr13:108279769
|
G | T | 12 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0002g0218others(9): Show | 12 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-7034G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279769 | ||||||
chr13:108279773
|
C | G | 3 | a0001c0001t0001g0358a0001c0001t0006g0279a0001c0001t0006g0280 | 3 | HG01943.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.425-7030C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279773 | ||||||
chr13:108279892
|
T | A | 1 | a0001c0001t0003g0167 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.425-6911T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279892 | ||||||
chr13:108279897
|
T | G | 2 | a0001c0001t0006g0279a0001c0001t0006g0280 | 2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.425-6906T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279897 | ||||||
chr13:108279961
|
C | T | 1 | a0001c0001t0015g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425-6842C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279961 | ||||||
chr13:108280040
|
A | G | 1 | a0001c0001t0013g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-6763A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280040 | ||||||
chr13:108280063
|
C | T | 2 | a0001c0001t0006g0164a0001c0001t0012g0163 | 2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425-6740C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280063 | ||||||
chr13:108280069
|
C | CT | 101 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0143others(98): Show | 106 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.425-6716dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280069 | |||||
chr13:108280069
|
C | CTT | 23 | a0001c0001t0002g0146a0001c0001t0002g0355a0001c0001t0003g0293others(20): Show | 25 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.425-6717_425-6716d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280069 | |||||
chr13:108280072
|
T | C | 1 | a0001c0001t0022g0089 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-6731T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280072 | ||||||
chr13:108280236
|
G | A | 1 | a0001c0001t0010g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-6567G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280236 | ||||||
chr13:108280245
|
A | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-6558A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280245 | ||||||
chr13:108280513
|
T | C | 1 | a0001c0001t0002g0335 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.425-6290T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280513 | ||||||
chr13:108280561
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.425-6242G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280561 | ||||||
chr13:108280716
|
C | CT | 34 | a0001c0001t0002g0355a0001c0001t0003g0034a0001c0001t0003g0103others(31): Show | 36 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.425-6074dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280716 | |||||
chr13:108280716
|
CT | C | 26 | a0001c0001t0001g0323a0001c0001t0001g0326a0001c0001t0002g0041others(23): Show | 28 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.425-6074delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280716 | |||||
chr13:108280725
|
T | G | 20 | a0001c0001t0002g0124a0001c0001t0002g0129a0001c0001t0002g0139others(17): Show | 22 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.425-6078T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280725 | ||||||
chr13:108280820
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0006g0212 | 2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.425-5983G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280820 | ||||||
chr13:108280829
|
C | T | 1 | a0001c0001t0013g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-5974C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280829 | ||||||
chr13:108280866
|
A | G | 1 | a0001c0001t0015g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425-5937A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280866 | ||||||
chr13:108280891
|
A | G | 1 | a0001c0001t0008g0185 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.425-5912A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280891 | ||||||
chr13:108280958
|
T | TATTAGAG others(3): Show |
2 | a0001c0001t0002g0007a0001c0001t0002g0025 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-5834_425-5825d others(12): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280958 | |||||
chr13:108281007
|
G | A | 12 | a0001c0001t0001g0165a0001c0001t0001g0181a0001c0001t0001g0227others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-5796G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281007 | ||||||
chr13:108281115
|
A | G | 1 | a0001c0001t0002g0270 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.425-5688A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281115 | ||||||
chr13:108281129
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.425-5674C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281129 | ||||||
chr13:108281153
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.425-5650A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281153 | ||||||
chr13:108281315
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-5488T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281315 | ||||||
chr13:108281601
|
A | G | 2 | a0001c0001t0001g0297a0001c0001t0002g0218 | 2 | HG00323.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.425-5202A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281601 | ||||||
chr13:108281663
|
A | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0058a0001c0001t0001g0086others(23): Show | 27 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.425-5140A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281663 | ||||||
chr13:108281697
|
G | A | 236 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(233): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.425-5106G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281697 | ||||||
chr13:108281867
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-4936T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281867 | ||||||
chr13:108281948
|
C | T | 9 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0003g0269others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-4855C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281948 | ||||||
chr13:108282055
|
G | A | 6 | a0001c0001t0001g0228a0001c0001t0006g0022a0001c0001t0006g0090others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-4748G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282055 | ||||||
chr13:108282260
|
ATG | A | 7 | a0001c0001t0001g0057a0001c0001t0002g0288a0001c0001t0006g0279others(4): Show | 7 | HG01943.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-4541_425-4540d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108282260 | |||||
chr13:108282266
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-4537T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282266 | ||||||
chr13:108282272
|
G | A | 98 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(95): Show | 103 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.425-4531G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282272 | ||||||
chr13:108282276
|
A | G | 7 | a0001c0001t0009g0208a0001c0001t0015g0311a0001c0001t0016g0201others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-4527A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282276 | ||||||
chr13:108282346
|
A | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-4457A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282346 | ||||||
chr13:108282550
|
G | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0259a0001c0001t0001g0278others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-4253G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282550 | ||||||
chr13:108282735
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.425-4068T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282735 | ||||||
chr13:108282803
|
G | A | 7 | a0001c0001t0001g0228a0001c0001t0006g0022a0001c0001t0006g0090others(4): Show | 7 | HG01243.hp2 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-4000G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282803 | ||||||
chr13:108282886
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-3917T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282886 | ||||||
chr13:108282960
|
A | C | 9 | a0001c0001t0001g0252a0001c0001t0001g0297a0001c0001t0001g0305others(6): Show | 10 | HG00741.hp2 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.425-3843A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282960 | ||||||
chr13:108283099
|
C | T | 100 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(97): Show | 106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.425-3704C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283099 | ||||||
chr13:108283147
|
G | C | 1 | a0001c0001t0005g0265 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.425-3656G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283147 | ||||||
chr13:108283209
|
G | A | 99 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(96): Show | 105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.425-3594G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283209 | ||||||
chr13:108283221
|
C | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0160 | 2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.425-3582C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283221 | ||||||
chr13:108283341
|
A | G | 104 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-3462A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283341 | ||||||
chr13:108283375
|
T | G | 34 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.425-3428T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283375 | ||||||
chr13:108283443
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0259a0001c0001t0001g0278others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-3360A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283443 | ||||||
chr13:108283554
|
A | T | 101 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(98): Show | 107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-3249A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283554 | ||||||
chr13:108283573
|
T | A | 1 | a0001c0001t0012g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-3230T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283573 | ||||||
chr13:108283580
|
A | G | 1 | a0001c0001t0014g0081 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.425-3223A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283580 | ||||||
chr13:108283588
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.425-3215T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283588 | ||||||
chr13:108283688
|
A | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-3115A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283688 | ||||||
chr13:108283733
|
C | T | 8 | a0001c0001t0001g0143a0001c0001t0001g0296a0001c0001t0002g0002others(5): Show | 9 | HG00140.hp1 HG01074.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-3070C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283733 | ||||||
chr13:108283813
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2990T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283813 | ||||||
chr13:108283822
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2981T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283822 | ||||||
chr13:108283823
|
A | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2980A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283823 | ||||||
chr13:108283824
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2979G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283824 | ||||||
chr13:108283839
|
T | C | 51 | a0001c0001t0001g0006a0001c0001t0001g0228a0001c0001t0001g0259others(48): Show | 54 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.425-2964T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283839 | ||||||
chr13:108283914
|
T | C | 101 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(98): Show | 107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-2889T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283914 | ||||||
chr13:108283987
|
T | A | 1 | a0001c0001t0007g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.425-2816T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283987 | ||||||
chr13:108284025
|
G | C | 2 | a0001c0001t0005g0064a0001c0001t0009g0260 | 2 | NA18983.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.425-2778G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284025 | ||||||
chr13:108284091
|
G | C | 1 | a0001c0001t0012g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-2712G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284091 | ||||||
chr13:108284094
|
G | C | 1 | a0001c0001t0001g0300 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.425-2709G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284094 | ||||||
chr13:108284100
|
T | C | 101 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(98): Show | 107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-2703T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284100 | ||||||
chr13:108284201
|
C | G | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2602C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284201 | ||||||
chr13:108284202
|
A | C | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2601A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284202 | ||||||
chr13:108284203
|
C | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2600C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284203 | ||||||
chr13:108284277
|
T | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0326a0001c0001t0006g0075others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2526T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284277 | ||||||
chr13:108284303
|
T | C | 1 | a0001c0001t0005g0356 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.425-2500T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284303 | ||||||
chr13:108284307
|
C | A | 1 | a0001c0001t0005g0065 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.425-2496C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284307 | ||||||
chr13:108284351
|
TAAATGAA others(17): Show |
T | 101 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(98): Show | 107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-2448_425-2425d others(26): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284351 | |||||
chr13:108284352
|
A | G | 4 | a0001c0001t0006g0202a0001c0001t0009g0207a0001c0001t0028g0156others(1): Show | 4 | HG00099.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-2451A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284352 | ||||||
chr13:108284355
|
TGAATAAA others(5): Show |
T | 1 | a0001c0001t0033g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.425-2447_425-2436d others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284355 | ||||||
chr13:108284356
|
G | A | 3 | a0001c0001t0006g0202a0001c0001t0009g0207a0001c0001t0028g0156 | 3 | HG02622.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.425-2447G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284356 | ||||||
chr13:108284356
|
GAATA | G | 36 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0034others(33): Show | 37 | HG01069.hp2 HG01257.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.425-2440_425-2437d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284356 | |||||
chr13:108284359
|
T | C | 3 | a0001c0001t0006g0202a0001c0001t0009g0207a0001c0001t0028g0156 | 3 | HG02622.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.425-2444T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284359 | ||||||
chr13:108284363
|
T | C | 9 | a0001c0001t0001g0228a0001c0001t0004g0189a0001c0001t0004g0337others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-2440T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284363 | ||||||
chr13:108284363
|
T | TAAAC | 5 | a0001c0001t0001g0006a0001c0001t0001g0259a0001c0001t0001g0278others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-2417_425-2414d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284363 | |||||
chr13:108284363
|
TAAAC | T | 11 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 12 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-2417_425-2414d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284363 | |||||
chr13:108284367
|
C | T | 84 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0051others(81): Show | 87 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.425-2436C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284367 | ||||||
chr13:108284371
|
C | T | 8 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0171others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-2432C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284371 | ||||||
chr13:108284383
|
C | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2420C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284383 | ||||||
chr13:108284384
|
A | C | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2419A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284384 | ||||||
chr13:108284387
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2416C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284387 | ||||||
chr13:108284496
|
T | C | 1 | a0001c0001t0003g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.425-2307T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284496 | ||||||
chr13:108284623
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2180T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284623 | ||||||
chr13:108284690
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.425-2113C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284690 | ||||||
chr13:108284820
|
G | T | 41 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0181others(38): Show | 44 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.425-1983G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284820 | ||||||
chr13:108284965
|
T | C | 6 | a0001c0001t0001g0023a0001c0001t0002g0142a0001c0001t0002g0162others(3): Show | 6 | HG00099.hp1 HG00735.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-1838T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284965 | ||||||
chr13:108285033
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-1770C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285033 | ||||||
chr13:108285104
|
T | A | 103 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(100): Show | 109 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.425-1699T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285104 | ||||||
chr13:108285143
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0358 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.425-1660G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285143 | ||||||
chr13:108285160
|
T | C | 1 | a0001c0001t0012g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-1643T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285160 | ||||||
chr13:108285212
|
A | AAGG | 353 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(350): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.425-1589_425-1588i others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108285212 | |||||
chr13:108285380
|
A | T | 1 | a0001c0001t0030g0195 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.425-1423A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285380 | ||||||
chr13:108285396
|
A | C | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-1407A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285396 | ||||||
chr13:108285485
|
A | G | 104 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-1318A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285485 | ||||||
chr13:108285492
|
A | G | 41 | a0001c0001t0001g0191a0001c0001t0001g0227a0001c0001t0001g0252others(38): Show | 44 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.425-1311A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285492 | ||||||
chr13:108285524
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.425-1279A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285524 | ||||||
chr13:108285589
|
G | A | 1 | a0001c0001t0012g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-1214G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285589 | ||||||
chr13:108285687
|
A | G | 1 | a0001c0001t0004g0284 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.425-1116A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285687 | ||||||
chr13:108285751
|
T | C | 1 | a0001c0001t0006g0226 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.425-1052T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285751 | ||||||
chr13:108285821
|
A | G | 1 | a0001c0001t0002g0304 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.425-982A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285821 | ||||||
chr13:108285905
|
T | C | 33 | a0001c0001t0002g0129a0001c0001t0002g0146a0001c0001t0002g0342others(30): Show | 36 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.425-898T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285905 | ||||||
chr13:108286003
|
A | T | 2 | a0001c0001t0003g0001a0001c0001t0003g0161 | 5 | NA18971.hp1 NA18983.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-800A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286003 | ||||||
chr13:108286070
|
G | T | 4 | a0001c0001t0009g0208a0001c0001t0015g0311a0001c0001t0019g0113others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-733G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286070 | ||||||
chr13:108286228
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0160 | 2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.425-575C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286228 | ||||||
chr13:108286321
|
G | A | 1 | a0001c0001t0004g0334 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.425-482G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286321 | ||||||
chr13:108286346
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0013g0187a0001c0001t0031g0221 | 3 | HG02055.hp1 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.425-457G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286346 | ||||||
chr13:108286349
|
T | C | 104 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-454T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286349 | ||||||
chr13:108286354
|
AT | A | 12 | a0001c0001t0001g0057a0001c0001t0001g0259a0001c0001t0002g0288others(9): Show | 12 | HG01074.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-438delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108286354 | |||||
chr13:108286373
|
T | G | 104 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-430T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286373 | ||||||
chr13:108286379
|
T | A | 104 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-424T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286379 | ||||||
chr13:108286386
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-417T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286386 | ||||||
chr13:108286600
|
A | G | 4 | a0001c0001t0002g0240a0001c0001t0008g0236a0001c0001t0008g0255others(1): Show | 4 | HG00280.hp2 HG02486.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-203A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286600 | ||||||
chr13:108286628
|
CAT | C | 102 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(99): Show | 107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-167_425-166del others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108286628 | |||||
chr13:108286636
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-167T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286636 | ||||||
chr13:108286700
|
AATTG | A | 4 | a0001c0001t0009g0208a0001c0001t0015g0311a0001c0001t0019g0113others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-99_425-96delGA others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108286700 | |||||
chr13:108286735
|
G | A | 1 | a0001c0001t0005g0336 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.425-68G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286735 | ||||||
chr13:108286750
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0012g0087 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.425-53T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286750 | ||||||
chr13:108286986
|
C | G | 3 | a0001c0001t0006g0022a0001c0001t0006g0054a0001c0001t0006g0199 | 3 | HG02630.hp1 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.481+127C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108286986 | ||||||
chr13:108287051
|
A | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+192A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287051 | ||||||
chr13:108287108
|
C | T | 2 | a0001c0001t0005g0351a0001c0001t0009g0327 | 2 | NA18974.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.481+249C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287108 | ||||||
chr13:108287121
|
G | A | 1 | a0001c0001t0004g0079 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.481+262G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287121 | ||||||
chr13:108287132
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0030g0195 | 2 | HG02055.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.481+273A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287132 | ||||||
chr13:108287133
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.481+274G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287133 | ||||||
chr13:108287139
|
A | G | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+280A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287139 | ||||||
chr13:108287253
|
T | G | 1 | a0001c0001t0002g0270 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.481+394T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287253 | ||||||
chr13:108287306
|
T | A | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+447T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287306 | ||||||
chr13:108287327
|
A | G | 4 | a0001c0001t0003g0188a0001c0001t0004g0048a0001c0001t0005g0082others(1): Show | 4 | HG00544.hp1 HG02015.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+468A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287327 | ||||||
chr13:108287357
|
A | C | 102 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(99): Show | 108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.481+498A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287357 | ||||||
chr13:108287415
|
A | T | 1 | a0001c0001t0002g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+556A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287415 | ||||||
chr13:108287508
|
C | T | 1 | a0001c0001t0012g0085 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.481+649C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287508 | ||||||
chr13:108287574
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0228a0001c0001t0001g0259others(18): Show | 22 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.481+715A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287574 | ||||||
chr13:108288060
|
G | A | 122 | a0001c0001t0001g0006a0001c0001t0001g0086a0001c0001t0001g0096others(119): Show | 128 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.481+1201G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288060 | ||||||
chr13:108288101
|
G | A | 7 | a0001c0001t0003g0034a0001c0001t0004g0029a0001c0001t0004g0334others(4): Show | 7 | HG02071.hp1 NA18962.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+1242G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288101 | ||||||
chr13:108288210
|
A | G | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.481+1351A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288210 | ||||||
chr13:108288400
|
C | A | 343 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(340): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.481+1541C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288400 | ||||||
chr13:108288571
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.481+1712A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288571 | ||||||
chr13:108288596
|
T | C | 1 | a0001c0001t0004g0276 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.481+1737T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288596 | ||||||
chr13:108288633
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.481+1774A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288633 | ||||||
chr13:108288822
|
C | T | 1 | a0001c0001t0007g0251 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.481+1963C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288822 | ||||||
chr13:108288823
|
G | A | 8 | a0001c0001t0001g0228a0001c0001t0006g0090a0001c0001t0006g0202others(5): Show | 8 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+1964G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288823 | ||||||
chr13:108288852
|
G | A | 1 | a0001c0001t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.481+1993G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288852 | ||||||
chr13:108288955
|
G | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0025 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.481+2096G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288955 | ||||||
chr13:108288966
|
T | A | 3 | a0001c0001t0016g0201a0001c0001t0016g0209a0001c0001t0020g0141 | 3 | HG01884.hp1 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.481+2107T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288966 | ||||||
chr13:108289067
|
G | C | 4 | a0001c0001t0009g0208a0001c0001t0015g0311a0001c0001t0019g0113others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+2208G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289067 | ||||||
chr13:108289091
|
C | CAGA | 104 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.481+2236_481+2238d others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108289091 | |||||
chr13:108289249
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.481+2390C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289249 | ||||||
chr13:108289347
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0259a0001c0001t0001g0278others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+2488C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289347 | ||||||
chr13:108289431
|
A | G | 1 | a0001c0001t0008g0211 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.481+2572A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289431 | ||||||
chr13:108289458
|
A | G | 1 | a0001c0001t0008g0211 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.481+2599A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289458 | ||||||
chr13:108289599
|
TATA | T | 14 | a0001c0001t0001g0228a0001c0001t0006g0072a0001c0001t0006g0090others(11): Show | 14 | HG01081.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.481+2747_481+2749d others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108289599 | |||||
chr13:108289634
|
T | A | 104 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.481+2775T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289634 | ||||||
chr13:108289675
|
T | G | 1 | a0001c0001t0003g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.481+2816T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289675 | ||||||
chr13:108289684
|
A | G | 2 | a0001c0001t0013g0074a0001c0001t0013g0243 | 2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.481+2825A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289684 | ||||||
chr13:108289801
|
T | C | 1 | a0001c0001t0003g0237 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.481+2942T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289801 | ||||||
chr13:108290248
|
A | G | 102 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(99): Show | 107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.481+3389A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290248 | ||||||
chr13:108290440
|
G | C | 68 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0050others(65): Show | 74 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.481+3581G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290440 | ||||||
chr13:108290528
|
T | G | 1 | a0001c0001t0006g0121 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.481+3669T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290528 | ||||||
chr13:108290631
|
G | A | 1 | a0001c0001t0006g0279 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.481+3772G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290631 | ||||||
chr13:108290681
|
A | C | 3 | a0001c0001t0006g0202a0001c0001t0009g0207a0001c0001t0028g0156 | 3 | HG02622.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.481+3822A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290681 | ||||||
chr13:108290686
|
A | G | 102 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(99): Show | 107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.481+3827A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290686 | ||||||
chr13:108290720
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0228a0001c0001t0001g0259others(18): Show | 22 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.481+3861C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290720 | ||||||
chr13:108290869
|
C | A | 101 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(98): Show | 106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.481+4010C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290869 | ||||||
chr13:108290967
|
G | A | 2 | a0001c0001t0002g0306a0001c0001t0008g0211 | 2 | HG01261.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.481+4108G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290967 | ||||||
chr13:108290990
|
C | T | 2 | a0001c0001t0003g0120a0001c0001t0007g0119 | 2 | NA19057.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.481+4131C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290990 | ||||||
chr13:108291267
|
A | T | 1 | a0001c0001t0006g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.481+4408A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291267 | ||||||
chr13:108291327
|
C | G | 1 | a0001c0001t0006g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+4468C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291327 | ||||||
chr13:108291382
|
T | G | 361 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(358): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.481+4523T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291382 | ||||||
chr13:108291395
|
T | C | 2 | a0001c0001t0006g0072a0001c0001t0006g0280 | 2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.481+4536T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291395 | ||||||
chr13:108291441
|
A | G | 33 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0034others(30): Show | 35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.481+4582A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291441 | ||||||
chr13:108291842
|
T | C | 1 | a0001c0001t0005g0346 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.481+4983T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291842 | ||||||
chr13:108291922
|
C | T | 1 | a0001c0001t0006g0121 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.481+5063C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291922 | ||||||
chr13:108291927
|
A | G | 7 | a0001c0001t0002g0007a0001c0001t0002g0025a0001c0001t0002g0147others(4): Show | 8 | HG01099.hp1 HG01169.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+5068A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291927 | ||||||
chr13:108291955
|
C | T | 1 | a0001c0001t0008g0019 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.481+5096C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291955 | ||||||
chr13:108292059
|
ACT | A | 101 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(98): Show | 106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.481+5207_481+5208d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108292059 | |||||
chr13:108292108
|
A | G | 41 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0181others(38): Show | 44 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.481+5249A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292108 | ||||||
chr13:108292171
|
T | C | 33 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0034others(30): Show | 35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.481+5312T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292171 | ||||||
chr13:108292423
|
A | G | 1 | a0001c0001t0002g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.481+5564A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292423 | ||||||
chr13:108292693
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481+5834T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292693 | ||||||
chr13:108292795
|
A | G | 1 | a0001c0001t0020g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.481+5936A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292795 | ||||||
chr13:108293265
|
T | C | 1 | a0001c0001t0002g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.481+6406T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293265 | ||||||
chr13:108293287
|
C | T | 1 | a0001c0001t0006g0056 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.481+6428C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293287 | ||||||
chr13:108293437
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.481+6578G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293437 | ||||||
chr13:108293592
|
A | C | 2 | a0001c0001t0006g0127a0001c0001t0006g0198 | 2 | HG00140.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.481+6733A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293592 | ||||||
chr13:108293654
|
T | C | 3 | a0001c0001t0006g0054a0001c0001t0006g0199a0001c0001t0009g0294 | 3 | HG01074.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.481+6795T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293654 | ||||||
chr13:108293783
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0013g0074a0001c0001t0013g0187others(2): Show | 5 | HG02055.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+6924G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293783 | ||||||
chr13:108293894
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0259a0001c0001t0001g0278others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+7035T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293894 | ||||||
chr13:108293951
|
C | T | 1 | a0001c0001t0008g0019 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.481+7092C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293951 | ||||||
chr13:108294183
|
A | AT | 108 | a0001c0001t0001g0086a0001c0001t0001g0096a0001c0001t0001g0098others(105): Show | 114 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.481+7338dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294183 | |||||
chr13:108294183
|
A | ATT | 7 | a0001c0001t0001g0227a0001c0001t0006g0224a0001c0001t0006g0225others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+7337_481+7338d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294183 | |||||
chr13:108294183
|
AT | A | 42 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0181others(39): Show | 45 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.481+7338delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294183 | |||||
chr13:108294242
|
T | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0228a0001c0001t0001g0259others(19): Show | 23 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.481+7383T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294242 | ||||||
chr13:108294324
|
C | T | 4 | a0001c0001t0009g0208a0001c0001t0015g0311a0001c0001t0019g0113others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+7465C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294324 | ||||||
chr13:108294380
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.481+7521A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294380 | ||||||
chr13:108294381
|
T | C | 1 | a0001c0001t0005g0265 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.481+7522T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294381 | ||||||
chr13:108294427
|
GC | G | 33 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0034others(30): Show | 35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.481+7570delC | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294427 | |||||
chr13:108294524
|
C | T | 1 | a0001c0001t0013g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.481+7665C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294524 | ||||||
chr13:108294550
|
A | AT | 7 | a0001c0001t0003g0110a0001c0001t0006g0038a0001c0001t0006g0039others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+7701dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294550 | |||||
chr13:108294550
|
AT | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0259a0001c0001t0001g0278others(5): Show | 9 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+7701delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294550 | |||||
chr13:108294671
|
G | A | 3 | a0001c0001t0006g0054a0001c0001t0006g0199a0001c0001t0009g0294 | 3 | HG01074.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.481+7812G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294671 | ||||||
chr13:108294672
|
T | C | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7813T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294672 | ||||||
chr13:108294677
|
T | G | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7818T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294677 | ||||||
chr13:108294678
|
T | TTCAC | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7820_481+7821i others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294678 | |||||
chr13:108294683
|
G | T | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7824G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294683 | ||||||
chr13:108294684
|
G | T | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7825G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294684 | ||||||
chr13:108294685
|
T | A | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7826T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294685 | ||||||
chr13:108294687
|
T | TA | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7828_481+7829i others(3): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294687 | ||||||
chr13:108294688
|
C | A | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7829C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294688 | ||||||
chr13:108294692
|
G | T | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7833G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294692 | ||||||
chr13:108294697
|
GCAT | G | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7839_481+7841d others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294697 | ||||||
chr13:108294702
|
GATATCAG others(4751): Show |
G | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7844_482-3793d others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294702 | ||||||
chr13:108294862
|
T | C | 1 | a0001c0001t0007g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.481+8003T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294862 | ||||||
chr13:108294864
|
G | T | 1 | a0001c0001t0007g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.481+8005G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294864 | ||||||
chr13:108295282
|
C | T | 1 | a0001c0001t0007g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.482-7971C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295282 | ||||||
chr13:108295283
|
T | C | 1 | a0001c0001t0007g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.482-7970T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295283 | ||||||
chr13:108295393
|
A | G | 224 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0050others(221): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.482-7860A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295393 | ||||||
chr13:108295480
|
C | T | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-7773C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295480 | ||||||
chr13:108295492
|
T | C | 1 | a0001c0001t0007g0258 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.482-7761T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295492 | ||||||
chr13:108295782
|
T | C | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-7471T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295782 | ||||||
chr13:108295843
|
T | G | 3 | a0001c0001t0016g0201a0001c0001t0016g0209a0001c0001t0020g0141 | 3 | HG01884.hp1 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.482-7410T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295843 | ||||||
chr13:108295968
|
G | T | 2 | a0001c0001t0005g0093a0001c0001t0005g0340 | 2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.482-7285G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295968 | ||||||
chr13:108296247
|
A | G | 1 | a0001c0001t0004g0284 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.482-7006A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296247 | ||||||
chr13:108296259
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.482-6994A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296259 | ||||||
chr13:108296305
|
G | A | 33 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0034others(30): Show | 35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-6948G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296305 | ||||||
chr13:108296544
|
C | T | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-6709C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296544 | ||||||
chr13:108296635
|
A | C | 1 | a0001c0001t0015g0311 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.482-6618A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296635 | ||||||
chr13:108296722
|
T | C | 1 | a0001c0001t0012g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.482-6531T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296722 | ||||||
chr13:108296891
|
A | G | 8 | a0001c0001t0001g0057a0001c0001t0001g0323a0001c0001t0002g0288others(5): Show | 8 | HG01943.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-6362A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296891 | ||||||
chr13:108297003
|
C | T | 3 | a0001c0001t0006g0054a0001c0001t0006g0199a0001c0001t0009g0294 | 3 | HG01074.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.482-6250C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297003 | ||||||
chr13:108297060
|
T | C | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-6193T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297060 | ||||||
chr13:108297099
|
T | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0140a0001c0001t0001g0259others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-6154T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297099 | ||||||
chr13:108297102
|
A | G | 1 | a0001c0001t0011g0302 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.482-6151A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297102 | ||||||
chr13:108297375
|
C | T | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-5878C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297375 | ||||||
chr13:108297519
|
C | A | 1 | a0001c0001t0001g0050 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.482-5734C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297519 | ||||||
chr13:108297616
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0358 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.482-5637T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297616 | ||||||
chr13:108297638
|
T | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0140a0001c0001t0001g0259others(4): Show | 8 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-5615T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297638 | ||||||
chr13:108297658
|
T | A | 2 | a0001c0001t0006g0072a0001c0001t0006g0280 | 2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.482-5595T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297658 | ||||||
chr13:108297735
|
G | A | 6 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0181others(3): Show | 6 | HG02622.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-5518G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297735 | ||||||
chr13:108297736
|
G | A | 1 | a0001c0001t0006g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.482-5517G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297736 | ||||||
chr13:108297796
|
A | C | 1 | a0001c0001t0006g0198 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.482-5457A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297796 | ||||||
chr13:108298013
|
A | G | 1 | a0001c0001t0012g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.482-5240A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298013 | ||||||
chr13:108298021
|
G | A | 332 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0030others(329): Show | 353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.482-5232G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298021 | ||||||
chr13:108298102
|
G | A | 1 | a0001c0001t0025g0047 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.482-5151G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298102 | ||||||
chr13:108298179
|
G | A | 30 | a0001c0001t0002g0129a0001c0001t0002g0146a0001c0001t0003g0060others(27): Show | 33 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.482-5074G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298179 | ||||||
chr13:108298199
|
T | G | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-5054T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298199 | ||||||
chr13:108298270
|
G | T | 106 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0092others(103): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.482-4983G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298270 | ||||||
chr13:108298489
|
A | G | 1 | a0001c0001t0008g0076 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.482-4764A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298489 | ||||||
chr13:108298704
|
C | T | 1 | a0001c0001t0012g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.482-4549C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298704 | ||||||
chr13:108298729
|
C | A | 7 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0071others(4): Show | 8 | HG01069.hp2 HG01257.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-4524C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298729 | ||||||
chr13:108298828
|
C | T | 32 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0034others(29): Show | 33 | HG01069.hp2 HG01257.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.482-4425C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298828 | ||||||
chr13:108298863
|
C | T | 1 | a0001c0001t0007g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.482-4390C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298863 | ||||||
chr13:108298879
|
G | A | 4 | a0001c0001t0006g0090a0001c0002t0002g0024a0001c0002t0021g0229others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-4374G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298879 | ||||||
chr13:108298949
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0358 | 2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.482-4304G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298949 | ||||||
chr13:108298968
|
A | AAAAC | 3 | a0001c0001t0007g0008a0001c0001t0007g0043a0001c0001t0007g0100 | 4 | HG01496.hp1 HG01928.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-4265_482-4262d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108298968 | |||||
chr13:108298972
|
CAAACAAA others(12): Show |
C | 33 | a0001c0001t0001g0341a0001c0001t0003g0010a0001c0001t0003g0034others(30): Show | 35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-4260_482-4242d others(21): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108298972 | |||||
chr13:108299158
|
G | A | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-4095G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299158 | ||||||
chr13:108299163
|
A | C | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-4090A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299163 | ||||||
chr13:108299251
|
G | A | 2 | a0001c0001t0006g0038a0001c0001t0006g0039 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-4002G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299251 | ||||||
chr13:108299297
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.482-3956G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299297 | ||||||
chr13:108299462
|
G | C | 29 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0069others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-3791G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299462 | ||||||
chr13:108299495
|
G | A | 1 | a0001c0001t0010g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.482-3758G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299495 | ||||||
chr13:108299537
|
T | C | 1 | a0001c0001t0006g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.482-3716T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299537 | ||||||
chr13:108299651
|
T | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0069a0001c0001t0001g0070others(21): Show | 24 | HG00099.hp1 HG00735.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-3602T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299651 | ||||||
chr13:108299962
|
G | A | 1 | a0001c0001t0006g0279 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.482-3291G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299962 | ||||||
chr13:108299994
|
T | C | 2 | a0001c0001t0004g0080a0001c0001t0004g0329 | 2 | NA18957.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.482-3259T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299994 | ||||||
chr13:108300010
|
G | A | 4 | a0001c0001t0006g0022a0001c0001t0006g0054a0001c0001t0006g0199others(1): Show | 4 | HG01074.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-3243G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300010 | ||||||
chr13:108300159
|
C | G | 52 | a0001c0001t0001g0050a0001c0001t0001g0264a0001c0001t0002g0197others(49): Show | 55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.482-3094C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300159 | ||||||
chr13:108300204
|
A | G | 1 | a0001c0001t0004g0249 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.482-3049A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300204 | ||||||
chr13:108300205
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0006g0220 | 2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.482-3048T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300205 | ||||||
chr13:108300343
|
C | T | 1 | a0001c0001t0006g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.482-2910C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300343 | ||||||
chr13:108300354
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.482-2899A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300354 | ||||||
chr13:108300420
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0259a0001c0001t0001g0278others(3): Show | 7 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-2833C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300420 | ||||||
chr13:108300430
|
A | G | 1 | a0001c0001t0005g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.482-2823A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300430 | ||||||
chr13:108300665
|
T | C | 1 | a0001c0001t0003g0350 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.482-2588T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300665 | ||||||
chr13:108300949
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0004g0118 | 2 | HG02040.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.482-2304A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300949 | ||||||
chr13:108300968
|
G | A | 1 | a0001c0001t0005g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.482-2285G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300968 | ||||||
chr13:108301127
|
A | G | 1 | a0001c0001t0006g0121 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.482-2126A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301127 | ||||||
chr13:108301481
|
C | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0278a0001c0001t0001g0305 | 4 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-1772C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301481 | ||||||
chr13:108301503
|
A | G | 3 | a0001c0001t0016g0201a0001c0001t0016g0209a0001c0001t0020g0141 | 3 | HG01884.hp1 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.482-1750A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301503 | ||||||
chr13:108301601
|
A | G | 1 | a0001c0001t0011g0017 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.482-1652A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301601 | ||||||
chr13:108301611
|
A | G | 1 | a0001c0001t0006g0121 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.482-1642A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301611 | ||||||
chr13:108301643
|
C | T | 89 | a0001c0001t0001g0050a0001c0001t0001g0098a0001c0001t0001g0264others(86): Show | 92 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.482-1610C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301643 | ||||||
chr13:108301714
|
A | G | 1 | a0001c0001t0003g0120 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.482-1539A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301714 | ||||||
chr13:108301878
|
A | G | 5 | a0001c0001t0006g0022a0001c0001t0006g0054a0001c0001t0006g0075others(2): Show | 5 | HG02559.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-1375A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301878 | ||||||
chr13:108301904
|
T | G | 1 | a0001c0001t0024g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.482-1349T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301904 | ||||||
chr13:108301943
|
G | A | 8 | a0001c0001t0001g0112a0001c0001t0001g0160a0001c0001t0001g0165others(5): Show | 8 | HG01192.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-1310G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301943 | ||||||
chr13:108301956
|
A | C | 84 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0192others(81): Show | 88 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.482-1297A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301956 | ||||||
chr13:108302085
|
C | T | 2 | a0001c0001t0006g0164a0001c0001t0006g0184 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.482-1168C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302085 | ||||||
chr13:108302232
|
A | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0171others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1021A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302232 | ||||||
chr13:108302387
|
A | C | 1 | a0001c0001t0031g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.482-866A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302387 | ||||||
chr13:108302396
|
C | T | 2 | a0001c0001t0004g0109a0001c0001t0004g0284 | 2 | NA18948.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.482-857C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302396 | ||||||
chr13:108302537
|
TC | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0030others(263): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.482-710delC | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108302537 | |||||
chr13:108302552
|
A | G | 1 | a0001c0001t0024g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.482-701A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302552 | ||||||
chr13:108302674
|
C | T | 2 | a0001c0001t0002g0028a0001c0001t0002g0321 | 2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.482-579C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302674 | ||||||
chr13:108302728
|
G | A | 1 | a0001c0001t0005g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.482-525G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302728 | ||||||
chr13:108302771
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0050others(17): Show | 21 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.482-482C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302771 | ||||||
chr13:108303054
|
A | C | 1 | a0001c0001t0006g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.482-199A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303054 | ||||||
chr13:108303116
|
C | G | 278 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(275): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.482-137C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303116 | ||||||
chr13:108303181
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.482-72C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303181 | ||||||
chr13:108303227
|
C | T | 8 | a0001c0001t0013g0074a0001c0001t0013g0091a0001c0001t0013g0122others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-26C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303227 | ||||||
chr13:108303801
|
T | A | 2 | a0001c0001t0012g0085a0001c0001t0012g0163 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.745+197T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303801 | ||||||
chr13:108303814
|
A | G | 1 | a0001c0001t0005g0216 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.745+210A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303814 | ||||||
chr13:108303815
|
T | C | 1 | a0001c0001t0013g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.745+211T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303815 | ||||||
chr13:108303821
|
T | A | 280 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(277): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.745+217T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303821 | ||||||
chr13:108303958
|
T | C | 1 | a0001c0001t0035g0307 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.745+354T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303958 | ||||||
chr13:108303969
|
G | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(36): Show | 41 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.745+365G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303969 | ||||||
chr13:108304140
|
G | T | 5 | a0001c0001t0001g0086a0001c0001t0006g0038a0001c0001t0006g0039others(2): Show | 5 | HG01081.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+536G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304140 | ||||||
chr13:108304191
|
C | A | 1 | a0001c0001t0031g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.745+587C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304191 | ||||||
chr13:108304284
|
A | C | 2 | a0001c0001t0001g0157a0001c0001t0031g0221 | 2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.745+680A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304284 | ||||||
chr13:108304325
|
A | G | 1 | a0001c0001t0012g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.745+721A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304325 | ||||||
chr13:108304410
|
C | T | 281 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(278): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.745+806C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304410 | ||||||
chr13:108304446
|
A | G | 277 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(274): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.745+842A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304446 | ||||||
chr13:108304478
|
G | T | 276 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(273): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.745+874G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304478 | ||||||
chr13:108304489
|
G | A | 2 | a0001c0001t0019g0113a0001c0001t0019g0213 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.745+885G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304489 | ||||||
chr13:108304552
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.745+948A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304552 | ||||||
chr13:108304642
|
C | T | 276 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(273): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.745+1038C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304642 | ||||||
chr13:108304715
|
A | G | 100 | a0001c0001t0004g0009a0001c0001t0004g0012a0001c0001t0004g0014others(97): Show | 106 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.745+1111A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304715 | ||||||
chr13:108305015
|
G | A | 2 | a0001c0001t0006g0164a0001c0001t0006g0184 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.745+1411G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305015 | ||||||
chr13:108305250
|
A | G | 1 | a0001c0001t0009g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.746-1576A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305250 | ||||||
chr13:108305287
|
A | G | 5 | a0001c0001t0003g0115a0001c0001t0003g0152a0001c0001t0003g0167others(2): Show | 5 | HG02080.hp2 NA18946.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-1539A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305287 | ||||||
chr13:108305361
|
T | C | 1 | a0001c0001t0008g0190 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.746-1465T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305361 | ||||||
chr13:108305594
|
T | A | 277 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(274): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.746-1232T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305594 | ||||||
chr13:108305644
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.746-1182A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305644 | ||||||
chr13:108305728
|
A | G | 2 | a0001c0001t0005g0277a0001c0001t0005g0330 | 2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.746-1098A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305728 | ||||||
chr13:108306017
|
C | T | 28 | a0001c0001t0007g0003a0001c0001t0007g0008a0001c0001t0007g0011others(25): Show | 32 | HG00408.hp1 HG00597.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.746-809C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306017 | ||||||
chr13:108306020
|
C | T | 1 | a0001c0001t0004g0334 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.746-806C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306020 | ||||||
chr13:108306560
|
T | C | 2 | a0001c0001t0004g0062a0001c0001t0035g0307 | 2 | NA18612.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.746-266T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306560 | ||||||
chr13:108306654
|
A | T | 28 | a0001c0001t0007g0003a0001c0001t0007g0008a0001c0001t0007g0011others(25): Show | 32 | HG00408.hp1 HG00597.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.746-172A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306654 | ||||||
chr13:108306732
|
A | AT | 258 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(255): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.746-84dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr13 | 108306732 | |||||
chr13:108306732
|
A | ATT | 20 | a0001c0001t0004g0044a0001c0001t0004g0059a0001c0001t0004g0061others(17): Show | 20 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.746-85_746-84dupTT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr13 | 108306732 | |||||
chr13:108306737
|
T | G | 1 | a0001c0001t0016g0201 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.746-89T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306737 | ||||||
chr13:108306759
|
T | C | 1 | a0001c0001t0004g0357 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.746-67T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306759 | ||||||
chr13:108306765
|
A | C | 2 | a0001c0001t0005g0277a0001c0001t0005g0330 | 2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.746-61A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306765 | ||||||
chr13:108306804
|
C | T | 1 | a0001c0001t0008g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.746-22C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306804 |