geneid | 7060 |
---|---|
ensemblid | ENSG00000113296.14 |
hgncid | 11788 |
symbol | THBS4 |
name | thrombospondin 4 |
refseq_nuc | NM_003248.6 |
refseq_prot | NP_003239.2 |
ensembl_nuc | ENST00000350881.6 |
ensembl_prot | ENSP00000339730.2 |
mane_status | MANE Select |
chr | chr5 |
start | 80035348 |
end | 80083287 |
strand | + |
ver | v1.2 |
region | chr5:80035348-80083287 |
region5000 | chr5:80030348-80088287 |
regionname0 | THBS4_chr5_80035348_80083287 |
regionname5000 | THBS4_chr5_80030348_80088287 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 961 | 317 | 57 | 44 | 166 | 13 | 35 | 123 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002 | 0/0 | 961 | 57 | 10 | 16 | 23 | 2 | 6 | 21 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0003 | 0/0 | 961 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0004 | 0/0 | 961 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0005 | 0/0 | 961 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0006 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0007 | 0/0 | 961 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0008 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0009 | 0/0 | 961 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0010 | 0/0 | 961 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0011 | 0/0 | 961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2886 | 148 | 24 | 10 | 85 | 6 | 21 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0002 | 0/0 | 2886 | 88 | 14 | 23 | 36 | 5 | 10 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0003 | 0/0 | 2886 | 79 | 17 | 11 | 45 | 2 | 4 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0004 | 0/0 | 2886 | 38 | 10 | 16 | 5 | 2 | 5 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0005 | 0/0 | 2886 | 11 | 0 | 0 | 11 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0006 | 0/0 | 2886 | 7 | 0 | 7 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0007 | 0/0 | 2886 | 7 | 0 | 0 | 7 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0008 | 0/0 | 2886 | 4 | 3 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0009 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0010 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0011 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0012 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0013 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0014 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0015 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0016 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
c0017 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 337 | 378 | 76 | 64 | 181 | 15 | 41 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
t0002 | 0/0 | 337 | 7 | 0 | 0 | 7 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
t0003 | 0/0 | 337 | 5 | 0 | 4 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
t0004 | 1/0 | 337 | 2 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
t0005 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
t0006 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 7 | 0 | 1 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0002 | 0/0 | 9 | 0 | 2 | 5 | 2 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0019 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2886 | 148 | 24 | 10 | 85 | 6 | 21 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0002 | 0/0 | 2886 | 88 | 14 | 23 | 36 | 5 | 10 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0003 | 0/0 | 2886 | 79 | 17 | 11 | 45 | 2 | 4 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0010 | 0/0 | 2886 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0004 | 0/0 | 2886 | 38 | 10 | 16 | 5 | 2 | 5 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0005 | 0/0 | 2886 | 11 | 0 | 0 | 11 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0007 | 0/0 | 2886 | 7 | 0 | 0 | 7 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0013 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0003c0006 | 0/0 | 2886 | 7 | 0 | 7 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0004c0008 | 0/0 | 2886 | 4 | 3 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0005c0009 | 0/0 | 2886 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0006c0011 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0007c0014 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0008c0015 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0009c0016 | 0/0 | 2886 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0010c0012 | 0/0 | 2886 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0011c0017 | 0/0 | 2886 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3222 | 145 | 24 | 10 | 84 | 5 | 21 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0001t0004 | 1/0 | 3222 | 2 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0001t0005 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0002t0001 | 0/0 | 3222 | 83 | 14 | 19 | 36 | 5 | 9 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0002t0003 | 0/0 | 3222 | 5 | 0 | 4 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0003t0001 | 0/0 | 3222 | 78 | 17 | 11 | 44 | 2 | 4 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0003t0006 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0001c0010t0001 | 0/0 | 3222 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0004t0001 | 0/0 | 3222 | 38 | 10 | 16 | 5 | 2 | 5 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0005t0001 | 0/0 | 3222 | 11 | 0 | 0 | 11 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0007t0002 | 0/0 | 3222 | 7 | 0 | 0 | 7 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0002c0013t0001 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0003c0006t0001 | 0/0 | 3222 | 7 | 0 | 7 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0004c0008t0001 | 0/0 | 3222 | 4 | 3 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0005c0009t0001 | 0/0 | 3222 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0006c0011t0001 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0007c0014t0001 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0008c0015t0001 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0009c0016t0001 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0010c0012t0001 | 0/0 | 3222 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
a0011c0017t0001 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | copy fasta | chr5 | 80030348 | 80088287 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0004g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0002t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0001 | 0/0 | 10 | 0 | 7 | 0 | 1 | 2 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0003t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0010t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0001c0010t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0005t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0007t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0007t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0007t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0007t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0007t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0002c0013t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0003c0006t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0003c0006t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0003c0006t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0003c0006t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0004c0008t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0004c0008t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0005c0009t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0005c0009t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0005c0009t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0006c0011t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0007c0014t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0008c0015t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0009c0016t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0010c0012t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
a0011c0017t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0275 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0277 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00140 | hp2 | a0002 | c0004 | t0001 | g0031 | EUR | GBR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0001 | EUR | FIN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00408 | hp1 | a0002 | c0005 | t0001 | g0198 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00408 | hp2 | a0010 | c0012 | t0001 | g0005 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0211 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0246 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00642 | hp1 | a0002 | c0004 | t0001 | g0178 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0236 | EAS | CHS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00733 | hp1 | a0002 | c0004 | t0001 | g0250 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0226 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0030 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG00741 | hp2 | a0002 | c0004 | t0001 | g0249 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01069 | hp1 | a0002 | c0004 | t0001 | g0177 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0234 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0229 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01099 | hp2 | a0002 | c0004 | t0001 | g0227 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01106 | hp2 | a0001 | c0002 | t0003 | g0274 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01109 | hp2 | a0002 | c0004 | t0001 | g0028 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01167 | hp1 | a0002 | c0004 | t0001 | g0010 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0307 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01168 | hp2 | a0002 | c0004 | t0001 | g0319 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01169 | hp2 | a0002 | c0004 | t0001 | g0010 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01192 | hp2 | a0002 | c0004 | t0001 | g0228 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01243 | hp2 | a0004 | c0008 | t0001 | g0014 | AMR | PUR | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0281 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01258 | hp2 | a0003 | c0006 | t0001 | g0080 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01261 | hp1 | a0002 | c0004 | t0001 | g0180 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01346 | hp1 | a0002 | c0004 | t0001 | g0038 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01346 | hp2 | a0001 | c0003 | t0001 | g0030 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01515 | hp1 | a0002 | c0004 | t0001 | g0028 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0257 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0256 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01884 | hp1 | a0008 | c0015 | t0001 | g0022 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0241 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01891 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01952 | hp2 | a0003 | c0006 | t0001 | g0020 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01975 | hp1 | a0003 | c0006 | t0001 | g0002 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01978 | hp2 | a0002 | c0004 | t0001 | g0225 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02004 | hp1 | a0003 | c0006 | t0001 | g0007 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0293 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0205 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02040 | hp1 | a0002 | c0004 | t0001 | g0248 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02055 | hp2 | a0002 | c0004 | t0001 | g0322 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0237 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0232 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02148 | hp1 | a0003 | c0006 | t0001 | g0020 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02148 | hp2 | a0002 | c0004 | t0001 | g0039 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0167 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CDX | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02257 | hp1 | a0005 | c0009 | t0001 | g0308 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02273 | hp1 | a0003 | c0006 | t0001 | g0007 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02280 | hp1 | a0002 | c0004 | t0001 | g0184 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02280 | hp2 | a0002 | c0004 | t0001 | g0166 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02293 | hp1 | a0003 | c0006 | t0001 | g0007 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02293 | hp2 | a0002 | c0004 | t0001 | g0031 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0316 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0208 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02602 | hp1 | a0002 | c0004 | t0001 | g0182 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0273 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0304 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0175 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02683 | hp1 | a0002 | c0004 | t0001 | g0190 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02698 | hp2 | a0002 | c0004 | t0001 | g0185 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02723 | hp1 | a0001 | c0010 | t0001 | g0251 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0233 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02818 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02896 | hp2 | a0006 | c0011 | t0001 | g0222 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0144 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02965 | hp1 | a0001 | c0010 | t0001 | g0252 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03041 | hp1 | a0004 | c0008 | t0001 | g0269 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0169 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03130 | hp2 | a0011 | c0017 | t0001 | g0262 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0315 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0224 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03239 | hp2 | a0002 | c0004 | t0001 | g0188 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0170 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0240 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03486 | hp2 | a0002 | c0004 | t0001 | g0189 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0230 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03540 | hp1 | a0005 | c0009 | t0001 | g0287 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03579 | hp2 | a0002 | c0004 | t0001 | g0013 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03688 | hp1 | a0002 | c0013 | t0001 | g0099 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0270 | SAS | PJL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03942 | hp1 | a0009 | c0016 | t0001 | g0181 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | BEB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04199 | hp1 | a0002 | c0004 | t0001 | g0010 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0301 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0291 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18522 | hp2 | a0004 | c0008 | t0001 | g0014 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | CHB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18940 | hp2 | a0002 | c0004 | t0001 | g0187 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18942 | hp1 | a0002 | c0005 | t0001 | g0165 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0317 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18947 | hp2 | a0002 | c0007 | t0002 | g0027 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18948 | hp2 | a0002 | c0007 | t0002 | g0026 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18952 | hp1 | a0002 | c0007 | t0002 | g0163 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18954 | hp2 | a0002 | c0007 | t0002 | g0026 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18964 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18970 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18972 | hp2 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18973 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18974 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18978 | hp1 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18988 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18993 | hp1 | a0002 | c0007 | t0002 | g0027 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0196 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19002 | hp2 | a0002 | c0004 | t0001 | g0186 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19003 | hp1 | a0002 | c0005 | t0001 | g0216 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19006 | hp1 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0242 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19043 | hp1 | a0002 | c0004 | t0001 | g0193 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19043 | hp2 | a0004 | c0008 | t0001 | g0014 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19054 | hp2 | a0002 | c0004 | t0001 | g0183 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19056 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19058 | hp2 | a0002 | c0007 | t0002 | g0164 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19060 | hp2 | a0001 | c0003 | t0006 | g0172 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19064 | hp2 | a0002 | c0004 | t0001 | g0199 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19065 | hp1 | a0002 | c0005 | t0001 | g0215 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19075 | hp1 | a0002 | c0005 | t0001 | g0214 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19077 | hp2 | a0002 | c0005 | t0001 | g0192 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0238 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19079 | hp1 | a0002 | c0005 | t0001 | g0217 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19080 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19081 | hp1 | a0002 | c0005 | t0001 | g0201 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19089 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19091 | hp2 | a0002 | c0007 | t0002 | g0162 | EAS | JPT | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA19240 | hp2 | a0002 | c0004 | t0001 | g0200 | AFR | YRI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA20129 | hp2 | a0002 | c0004 | t0001 | g0321 | AFR | ASW | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0231 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0276 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA20805 | hp2 | a0007 | c0014 | t0001 | g0146 | EUR | TSI | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01123 | hp1 | a0002 | c0004 | t0001 | g0179 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0324 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03471 | hp1 | a0005 | c0009 | t0001 | g0300 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | MSL | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | USA | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0243 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0100 | REF | REF | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0019 | REF | REF | THBS4_chr5_80030348_80088287 | THBS4 | chr5 | 80030348 | 80088287 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80055899
|
G | A | 1 | a0006 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.407G>A | p.Arg136Gln | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/22 | 597/3222 | 407/2886 | 136/961 | chr5 | 80055899 | ||
chr5:80058737
|
A | G | 1 | a0011 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.679A>G | p.Met227Val | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/22 | 869/3222 | 679/2886 | 227/961 | chr5 | 80058737 | ||
chr5:80059736
|
C | T | 1 | a0005 | 3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.818C>T | p.Thr273Met | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/22 | 1008/3222 | 818/2886 | 273/961 | chr5 | 80059736 | ||
chr5:80061729
|
G | A | 1 | a0010 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.1022G>A | p.Cys341Tyr | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/22 | 1212/3222 | 1022/2886 | 341/961 | chr5 | 80061729 | ||
chr5:80065442
|
G | C | 3 | a0002a0006a0009 | 59 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(56): Show |
missense_variant | MODERATE | c.1159G>C | p.Ala387Pro | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/22 | 1349/3222 | 1159/2886 | 387/961 | chr5 | 80065442 | ||
chr5:80070405
|
A | C | 1 | a0008 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1447A>C | p.Lys483Gln | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 11/22 | 1637/3222 | 1447/2886 | 483/961 | chr5 | 80070405 | ||
chr5:80076898
|
G | A | 1 | a0004 | 4 | HG01243.hp2 HG03041.hp1 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.1936G>A | p.Val646Ile | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/22 | 2126/3222 | 1936/2886 | 646/961 | chr5 | 80076898 | ||
chr5:80078171
|
G | A | 1 | a0003 | 7 | HG01258.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
missense_variant | MODERATE | c.2209G>A | p.Val737Ile | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/22 | 2399/3222 | 2209/2886 | 737/961 | chr5 | 80078171 | ||
chr5:80079215
|
C | T | 1 | a0007 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.2468C>T | p.Ala823Val | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/22 | 2658/3222 | 2468/2886 | 823/961 | chr5 | 80079215 | ||
chr5:80080056
|
G | A | 1 | a0009 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2663G>A | p.Arg888Lys | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/22 | 2853/3222 | 2663/2886 | 888/961 | chr5 | 80080056 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80035615
|
C | T | 1 | a0002c0005 | 11 | HG00408.hp1 NA18942.hp1 NA18974.hp1 others(8): Show |
synonymous_variant | LOW | c.78C>T | p.Ala26Ala | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 268/3222 | 78/2886 | 26/961 | chr5 | 80035615 | ||
chr5:80055912
|
C | T | 5 | a0001c0002a0002c0007a0004c0008others(2): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
synonymous_variant | LOW | c.420C>T | p.Ser140Ser | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/22 | 610/3222 | 420/2886 | 140/961 | chr5 | 80055912 | ||
chr5:80056029
|
A | T | 11 | a0001c0002a0001c0003a0001c0010others(8): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
synonymous_variant | LOW | c.537A>T | p.Pro179Pro | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/22 | 727/3222 | 537/2886 | 179/961 | chr5 | 80056029 | ||
chr5:80065459
|
G | A | 1 | a0001c0010 | 2 | HG02723.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.1176G>A | p.Ser392Ser | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/22 | 1366/3222 | 1176/2886 | 392/961 | chr5 | 80065459 | ||
chr5:80068110
|
G | A | 1 | a0005c0009 | 3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.1332G>A | p.Gly444Gly | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/22 | 1522/3222 | 1332/2886 | 444/961 | chr5 | 80068110 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80035371
|
A | G | 20 | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(17): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
5_prime_UTR_variant | MODIFIER | c.-167A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 167 | chr5 | 80035371 | |||||
chr5:80035406
|
C | G | 1 | a0002c0007t0002 | 7 | NA18947.hp2 NA18948.hp2 NA18952.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-132C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 132 | chr5 | 80035406 | |||||
chr5:80035420
|
G | C | 1 | a0001c0001t0005 | 1 | NA19080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 118 | chr5 | 80035420 | |||||
chr5:80035461
|
A | G | 1 | a0001c0003t0006 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-77A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/22 | 77 | chr5 | 80035461 | |||||
chr5:80083266
|
G | A | 1 | a0001c0002t0003 | 5 | HG00733.hp2 HG01106.hp2 HG01256.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*125G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 22/22 | 125 | chr5 | 80083266 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:80035714
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.88+89C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80035714 | ||||||
chr5:80036039
|
A | G | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+414A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036039 | ||||||
chr5:80036196
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.88+571G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036196 | ||||||
chr5:80036325
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.88+700G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036325 | ||||||
chr5:80036519
|
A | G | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.88+894A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036519 | ||||||
chr5:80036544
|
T | G | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+919T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036544 | ||||||
chr5:80036554
|
C | A | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+929C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036554 | ||||||
chr5:80036644
|
G | A | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+1019G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036644 | ||||||
chr5:80036857
|
A | T | 1 | a0002c0004t0001g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.88+1232A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80036857 | ||||||
chr5:80037050
|
C | A | 2 | a0002c0004t0001g0038a0002c0004t0001g0039 | 2 | HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.88+1425C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037050 | ||||||
chr5:80037282
|
G | T | 1 | a0001c0002t0001g0320 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.88+1657G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037282 | ||||||
chr5:80037440
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88+1815G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037440 | ||||||
chr5:80037562
|
T | C | 3 | a0001c0001t0001g0043a0001c0003t0001g0041a0001c0003t0001g0042 | 3 | HG02559.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.88+1937T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037562 | ||||||
chr5:80037592
|
G | T | 194 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0001t0001g0253others(191): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.88+1967G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037592 | ||||||
chr5:80037664
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.88+2039T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037664 | ||||||
chr5:80037890
|
C | T | 1 | a0002c0004t0001g0319 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.89-2187C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80037890 | ||||||
chr5:80038104
|
A | T | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.89-1973A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038104 | ||||||
chr5:80038215
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.89-1862G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038215 | ||||||
chr5:80038287
|
A | G | 1 | a0001c0001t0001g0025 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.89-1790A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038287 | ||||||
chr5:80038403
|
T | C | 7 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0157others(4): Show | 7 | HG01358.hp1 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-1674T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038403 | ||||||
chr5:80038470
|
G | A | 102 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0003g0226others(99): Show | 128 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.89-1607G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038470 | ||||||
chr5:80038573
|
T | C | 1 | a0001c0002t0001g0247 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.89-1504T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038573 | ||||||
chr5:80038765
|
C | T | 82 | a0001c0001t0001g0253a0001c0002t0001g0006a0001c0002t0001g0015others(79): Show | 93 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.89-1312C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038765 | ||||||
chr5:80038940
|
A | G | 8 | a0001c0001t0001g0024a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 9 | HG00621.hp1 HG00673.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-1137A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038940 | ||||||
chr5:80038958
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.89-1119A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80038958 | ||||||
chr5:80039095
|
G | T | 1 | a0001c0002t0001g0318 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.89-982G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039095 | ||||||
chr5:80039149
|
T | C | 107 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0003g0226others(104): Show | 134 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.89-928T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039149 | ||||||
chr5:80039444
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.89-633A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039444 | ||||||
chr5:80039530
|
G | A | 1 | a0001c0001t0001g0025 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.89-547G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039530 | ||||||
chr5:80039663
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.89-414G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039663 | ||||||
chr5:80039883
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.89-194T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 1/21 | chr5 | 80039883 | ||||||
chr5:80040447
|
CG | C | 107 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0003g0226others(104): Show | 132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.292+174delG | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80040447 | |||||
chr5:80040454
|
G | T | 1 | a0001c0003t0001g0246 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.292+174G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040454 | ||||||
chr5:80040455
|
T | G | 1 | a0001c0003t0001g0246 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.292+175T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040455 | ||||||
chr5:80040868
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.292+588A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040868 | ||||||
chr5:80040888
|
G | T | 1 | a0001c0003t0001g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.292+608G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80040888 | ||||||
chr5:80040933
|
ACT | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 5 | HG03130.hp1 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+659_292+660del others(2): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80040933 | |||||
chr5:80041003
|
G | A | 1 | a0001c0002t0001g0247 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.292+723G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041003 | ||||||
chr5:80041153
|
C | T | 1 | a0001c0003t0001g0244 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.292+873C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041153 | ||||||
chr5:80041162
|
G | A | 1 | a0002c0005t0001g0165 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.292+882G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041162 | ||||||
chr5:80041203
|
T | A | 1 | a0002c0004t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.292+923T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041203 | ||||||
chr5:80041264
|
T | C | 1 | a0001c0003t0001g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.292+984T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041264 | ||||||
chr5:80041334
|
C | T | 109 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0003g0226others(106): Show | 134 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.292+1054C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041334 | ||||||
chr5:80041408
|
C | G | 3 | a0001c0003t0001g0241a0001c0003t0001g0242a0001c0003t0001g0243 | 3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.292+1128C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041408 | ||||||
chr5:80041418
|
C | T | 1 | a0001c0002t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.292+1138C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041418 | ||||||
chr5:80041484
|
C | T | 90 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(87): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+1204C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041484 | ||||||
chr5:80041543
|
G | A | 4 | a0001c0002t0001g0254a0001c0002t0001g0255a0001c0002t0001g0256others(1): Show | 4 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+1263G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041543 | ||||||
chr5:80041644
|
G | T | 1 | a0001c0003t0001g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292+1364G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041644 | ||||||
chr5:80041709
|
T | A | 1 | a0001c0003t0001g0168 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.292+1429T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041709 | ||||||
chr5:80041759
|
T | A | 3 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170 | 3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292+1479T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041759 | ||||||
chr5:80041772
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.292+1492T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041772 | ||||||
chr5:80041880
|
A | G | 1 | a0001c0001t0001g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292+1600A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041880 | ||||||
chr5:80041992
|
T | C | 1 | a0001c0003t0001g0171 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.292+1712T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80041992 | ||||||
chr5:80042310
|
C | T | 3 | a0001c0003t0001g0241a0001c0003t0001g0242a0001c0003t0001g0243 | 3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.292+2030C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042310 | ||||||
chr5:80042438
|
A | C | 2 | a0001c0003t0001g0238a0001c0003t0001g0239 | 2 | NA18975.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.292+2158A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042438 | ||||||
chr5:80042823
|
A | G | 200 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0219others(197): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.292+2543A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042823 | ||||||
chr5:80042869
|
G | A | 85 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(82): Show | 96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+2589G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042869 | ||||||
chr5:80042913
|
C | T | 90 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(87): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+2633C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042913 | ||||||
chr5:80042929
|
G | A | 2 | a0001c0003t0001g0173a0001c0003t0006g0172 | 2 | NA18973.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.292+2649G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80042929 | ||||||
chr5:80043224
|
C | T | 90 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(87): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+2944C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043224 | ||||||
chr5:80043347
|
G | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG00423.hp2 HG00597.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.292+3067G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043347 | ||||||
chr5:80043614
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.292+3334G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043614 | ||||||
chr5:80043997
|
C | T | 3 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257 | 3 | HG01515.hp2 HG01517.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.292+3717C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80043997 | ||||||
chr5:80044031
|
G | C | 90 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(87): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+3751G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044031 | ||||||
chr5:80044128
|
T | C | 90 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(87): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+3848T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044128 | ||||||
chr5:80044193
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | NA18957.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.292+3913C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044193 | ||||||
chr5:80044414
|
TA | T | 91 | a0001c0001t0001g0154a0001c0002t0001g0006a0001c0002t0001g0015others(88): Show | 102 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.292+4144delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80044414 | |||||
chr5:80044416
|
A | G | 1 | a0001c0003t0001g0315 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.292+4136A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044416 | ||||||
chr5:80044570
|
G | A | 85 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(82): Show | 96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+4290G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044570 | ||||||
chr5:80044644
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.292+4364C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044644 | ||||||
chr5:80044677
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292+4397G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044677 | ||||||
chr5:80044707
|
G | C | 85 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(82): Show | 96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+4427G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044707 | ||||||
chr5:80044730
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.292+4450A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044730 | ||||||
chr5:80044733
|
AT | A | 90 | a0001c0001t0001g0063a0001c0002t0001g0006a0001c0002t0001g0015others(87): Show | 101 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.292+4464delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80044733 | |||||
chr5:80044756
|
A | G | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+4476A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044756 | ||||||
chr5:80044886
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.292+4606T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044886 | ||||||
chr5:80044942
|
G | A | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+4662G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80044942 | ||||||
chr5:80044987
|
ATCTCTGA others(3): Show |
A | 3 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0257 | 3 | HG01515.hp2 HG01517.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.292+4713_292+4722d others(12): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80044987 | |||||
chr5:80045072
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.292+4792A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045072 | ||||||
chr5:80045339
|
A | C | 90 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(87): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+5059A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045339 | ||||||
chr5:80045399
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.292+5119G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045399 | ||||||
chr5:80045531
|
C | CT | 14 | a0001c0001t0001g0133a0001c0002t0001g0314a0001c0003t0001g0001others(11): Show | 24 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.292+5267dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80045531 | |||||
chr5:80045531
|
CT | C | 16 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0066others(13): Show | 16 | HG00621.hp2 HG01070.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.292+5267delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80045531 | |||||
chr5:80045552
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0040a0008c0015t0001g0022 | 3 | HG01884.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.292+5272C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045552 | ||||||
chr5:80045592
|
G | A | 2 | a0001c0002t0001g0139a0001c0002t0001g0140 | 2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.292+5312G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045592 | ||||||
chr5:80045640
|
C | G | 4 | a0001c0002t0003g0226a0002c0004t0001g0225a0002c0004t0001g0227others(1): Show | 4 | HG00733.hp2 HG01099.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+5360C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045640 | ||||||
chr5:80045671
|
T | C | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+5391T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045671 | ||||||
chr5:80045687
|
G | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.292+5407G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045687 | ||||||
chr5:80045746
|
A | G | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+5466A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045746 | ||||||
chr5:80045797
|
C | T | 1 | a0001c0002t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.292+5517C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045797 | ||||||
chr5:80045810
|
C | T | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.292+5530C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80045810 | ||||||
chr5:80046019
|
C | T | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.292+5739C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046019 | ||||||
chr5:80046021
|
A | T | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.292+5741A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046021 | ||||||
chr5:80046048
|
A | G | 90 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(87): Show | 103 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.292+5768A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046048 | ||||||
chr5:80046166
|
C | A | 94 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0003g0226others(91): Show | 119 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.292+5886C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046166 | ||||||
chr5:80046197
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.292+5917A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046197 | ||||||
chr5:80046603
|
T | C | 2 | a0001c0010t0001g0251a0001c0010t0001g0252 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.292+6323T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046603 | ||||||
chr5:80046695
|
C | T | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.292+6415C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046695 | ||||||
chr5:80046696
|
G | A | 85 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(82): Show | 96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.292+6416G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046696 | ||||||
chr5:80046713
|
A | G | 2 | a0001c0002t0001g0311a0001c0002t0001g0312 | 2 | HG02071.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.292+6433A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80046713 | ||||||
chr5:80047550
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.292+7270G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047550 | ||||||
chr5:80047632
|
A | AAT | 11 | a0001c0003t0001g0001a0001c0003t0001g0030a0001c0003t0001g0173others(8): Show | 21 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.292+7353_292+7354d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80047632 | |||||
chr5:80047634
|
T | TA | 98 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0003g0226others(95): Show | 115 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.292+7354_292+7355i others(3): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047634 | ||||||
chr5:80047635
|
T | A | 5 | a0001c0003t0001g0191a0001c0003t0006g0172a0002c0004t0001g0319others(2): Show | 5 | HG01168.hp2 NA18942.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+7355T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047635 | ||||||
chr5:80047636
|
T | A | 21 | a0001c0002t0003g0226a0002c0004t0001g0010a0002c0004t0001g0028others(18): Show | 24 | HG00642.hp1 HG00733.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.292+7356T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047636 | ||||||
chr5:80047692
|
G | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0036others(10): Show | 15 | HG01361.hp1 HG02698.hp1 HG03491.hp2 others(12): Show |
intron_variant | MODIFIER | c.292+7412G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047692 | ||||||
chr5:80047977
|
C | T | 1 | a0001c0003t0001g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.292+7697C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047977 | ||||||
chr5:80047979
|
C | G | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.292+7699C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80047979 | ||||||
chr5:80048306
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.293-7479C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048306 | ||||||
chr5:80048466
|
T | C | 105 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0003g0226others(102): Show | 130 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.293-7319T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048466 | ||||||
chr5:80048632
|
A | ATG | 12 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0079others(9): Show | 14 | HG01258.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.293-7121_293-7120d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
A | ATGTG | 58 | a0001c0001t0001g0043a0001c0001t0001g0077a0001c0001t0001g0078others(55): Show | 75 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.293-7123_293-7120d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
A | ATGTGTG | 54 | a0001c0002t0001g0259a0001c0002t0001g0272a0001c0002t0001g0275others(51): Show | 65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.293-7125_293-7120d others(8): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
A | ATGTGTGT others(1): Show |
36 | a0001c0002t0001g0033a0001c0002t0001g0254a0001c0002t0001g0265others(33): Show | 41 | HG00408.hp1 HG00597.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.293-7127_293-7120d others(10): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
A | ATGTGTGT others(3): Show |
17 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(14): Show | 17 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-7129_293-7120d others(12): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
A | ATGTGTGT others(5): Show |
12 | a0001c0002t0001g0032a0001c0002t0001g0255a0001c0002t0001g0258others(9): Show | 15 | HG01069.hp1 HG02071.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.293-7131_293-7120d others(14): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
ATG | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0044others(9): Show | 15 | HG00408.hp2 HG00621.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-7121_293-7120d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
ATGTG | A | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01123.hp2 HG02027.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-7123_293-7120d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048632
|
ATGTGTGT others(5): Show |
A | 5 | a0001c0003t0001g0323a0001c0003t0001g0324a0001c0010t0001g0251others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-7131_293-7120d others(14): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80048632 | |||||
chr5:80048795
|
T | C | 48 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(45): Show | 65 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.293-6990T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048795 | ||||||
chr5:80048837
|
T | C | 1 | a0001c0002t0001g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-6948T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80048837 | ||||||
chr5:80049098
|
C | T | 1 | a0002c0004t0001g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.293-6687C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049098 | ||||||
chr5:80049145
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.293-6640A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049145 | ||||||
chr5:80049314
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.293-6471G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049314 | ||||||
chr5:80049387
|
A | G | 1 | a0001c0003t0001g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.293-6398A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049387 | ||||||
chr5:80049726
|
G | T | 104 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0003t0001g0001others(101): Show | 129 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.293-6059G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049726 | ||||||
chr5:80049846
|
A | G | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-5939A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049846 | ||||||
chr5:80049978
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293-5807C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049978 | ||||||
chr5:80049982
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.293-5803C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049982 | ||||||
chr5:80049987
|
A | G | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-5798A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80049987 | ||||||
chr5:80050194
|
A | C | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02027.hp1 HG02129.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.293-5591A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050194 | ||||||
chr5:80050361
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.293-5424T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050361 | ||||||
chr5:80050519
|
A | C | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-5266A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050519 | ||||||
chr5:80050592
|
G | C | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-5193G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050592 | ||||||
chr5:80050620
|
T | G | 1 | a0001c0003t0001g0223 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.293-5165T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050620 | ||||||
chr5:80050744
|
G | C | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-5041G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050744 | ||||||
chr5:80050776
|
G | A | 85 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(82): Show | 96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.293-5009G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050776 | ||||||
chr5:80050809
|
A | G | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-4976A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050809 | ||||||
chr5:80050984
|
A | G | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-4801A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80050984 | ||||||
chr5:80051057
|
C | T | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4728C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051057 | ||||||
chr5:80051215
|
A | G | 1 | a0001c0003t0001g0324 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.293-4570A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051215 | ||||||
chr5:80051304
|
C | T | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-4481C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051304 | ||||||
chr5:80051330
|
TAATAA | T | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4449_293-4445d others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80051330 | |||||
chr5:80051342
|
T | C | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4443T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051342 | ||||||
chr5:80051382
|
A | C | 4 | a0001c0002t0001g0254a0001c0002t0001g0255a0001c0002t0001g0256others(1): Show | 4 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-4403A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051382 | ||||||
chr5:80051425
|
T | C | 15 | a0001c0002t0001g0032a0001c0002t0001g0247a0001c0002t0001g0254others(12): Show | 18 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-4360T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051425 | ||||||
chr5:80051466
|
G | A | 10 | a0001c0002t0001g0032a0001c0002t0001g0247a0001c0002t0001g0254others(7): Show | 11 | HG01255.hp2 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-4319G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051466 | ||||||
chr5:80051513
|
C | G | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-4272C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051513 | ||||||
chr5:80051697
|
C | T | 2 | a0001c0002t0001g0306a0001c0002t0001g0307 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.293-4088C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051697 | ||||||
chr5:80051703
|
A | G | 1 | a0001c0002t0001g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.293-4082A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051703 | ||||||
chr5:80051816
|
G | C | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-3969G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051816 | ||||||
chr5:80051934
|
G | A | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-3851G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80051934 | ||||||
chr5:80052606
|
G | A | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-3179G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052606 | ||||||
chr5:80052616
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0003t0001g0041others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-3169A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052616 | ||||||
chr5:80052673
|
C | T | 5 | a0002c0007t0002g0026a0002c0007t0002g0027a0002c0007t0002g0162others(2): Show | 7 | NA18947.hp2 NA18948.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-3112C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052673 | ||||||
chr5:80052839
|
T | A | 2 | a0002c0004t0001g0013a0006c0011t0001g0222 | 4 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-2946T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052839 | ||||||
chr5:80052936
|
G | A | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-2849G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80052936 | ||||||
chr5:80053206
|
T | A | 1 | a0001c0002t0001g0312 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.293-2579T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053206 | ||||||
chr5:80053334
|
T | C | 11 | a0001c0003t0001g0001a0001c0003t0001g0030a0001c0003t0001g0173others(8): Show | 21 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.293-2451T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053334 | ||||||
chr5:80053406
|
C | CT | 6 | a0001c0001t0001g0059a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG00558.hp2 HG01981.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-2365dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053406 | |||||
chr5:80053406
|
CT | C | 201 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0124others(198): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.293-2365delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053406 | |||||
chr5:80053406
|
CTT | C | 4 | a0001c0002t0001g0272a0001c0002t0001g0284a0002c0004t0001g0013others(1): Show | 6 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-2366_293-2365d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053406 | |||||
chr5:80053582
|
C | G | 199 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0002t0001g0006others(196): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.293-2203C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053582 | ||||||
chr5:80053590
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.293-2195C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053590 | ||||||
chr5:80053611
|
TG | T | 44 | a0001c0001t0001g0043a0001c0001t0001g0219a0001c0003t0001g0041others(41): Show | 52 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.293-2172delG | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80053611 | |||||
chr5:80053766
|
T | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-2019T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053766 | ||||||
chr5:80053781
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-2004G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053781 | ||||||
chr5:80053955
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-1830G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80053955 | ||||||
chr5:80054134
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.293-1651C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054134 | ||||||
chr5:80054156
|
TTTC | T | 102 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(99): Show | 125 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.293-1626_293-1624d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054156 | |||||
chr5:80054157
|
TTC | T | 5 | a0002c0004t0001g0013a0002c0004t0001g0180a0002c0004t0001g0322others(2): Show | 7 | HG01261.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-1626_293-1625d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054157 | |||||
chr5:80054159
|
C | CT | 4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0046others(1): Show | 7 | HG03130.hp1 HG03139.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-1611dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054159 | |||||
chr5:80054159
|
C | CTT | 85 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(82): Show | 98 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.293-1612_293-1611d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054159 | |||||
chr5:80054164
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293-1621T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054164 | ||||||
chr5:80054176
|
A | T | 3 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170 | 3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.293-1609A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054176 | ||||||
chr5:80054185
|
C | T | 1 | a0001c0003t0001g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-1600C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054185 | ||||||
chr5:80054217
|
C | T | 2 | a0001c0010t0001g0251a0001c0010t0001g0252 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.293-1568C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054217 | ||||||
chr5:80054262
|
C | T | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.293-1523C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054262 | ||||||
chr5:80054318
|
C | CT | 5 | a0001c0001t0001g0016a0001c0001t0001g0076a0001c0001t0001g0112others(2): Show | 6 | HG01361.hp1 HG02698.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-1447dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054318 | |||||
chr5:80054318
|
CTTTT | C | 107 | a0001c0002t0001g0259a0001c0002t0001g0271a0001c0003t0001g0001others(104): Show | 132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.293-1450_293-1447d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054318 | |||||
chr5:80054318
|
CTTTTT | C | 89 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(86): Show | 102 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.293-1451_293-1447d others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80054318 | |||||
chr5:80054342
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.293-1443A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054342 | ||||||
chr5:80054373
|
T | A | 2 | a0001c0003t0001g0175a0001c0003t0001g0176 | 2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.293-1412T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054373 | ||||||
chr5:80054462
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-1323G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054462 | ||||||
chr5:80054556
|
T | C | 1 | a0001c0002t0001g0286 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.293-1229T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054556 | ||||||
chr5:80054610
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.293-1175C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054610 | ||||||
chr5:80054661
|
C | T | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-1124C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054661 | ||||||
chr5:80054903
|
T | C | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-882T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054903 | ||||||
chr5:80054944
|
C | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-841C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80054944 | ||||||
chr5:80055041
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.293-744G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055041 | ||||||
chr5:80055101
|
C | T | 3 | a0001c0003t0001g0175a0001c0003t0001g0176a0001c0003t0001g0245 | 3 | HG02258.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.293-684C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055101 | ||||||
chr5:80055112
|
G | A | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG02027.hp1 HG02129.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.293-673G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055112 | ||||||
chr5:80055131
|
G | A | 2 | a0002c0004t0001g0038a0002c0004t0001g0039 | 2 | HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.293-654G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055131 | ||||||
chr5:80055227
|
C | T | 282 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0016others(279): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.293-558C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055227 | ||||||
chr5:80055264
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.293-521G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055264 | ||||||
chr5:80055311
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.293-474G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055311 | ||||||
chr5:80055317
|
G | T | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-468G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055317 | ||||||
chr5:80055588
|
T | C | 196 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(193): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.293-197T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055588 | ||||||
chr5:80055593
|
GA | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-188delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr5 | 80055593 | |||||
chr5:80055721
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.293-64G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055721 | ||||||
chr5:80055721
|
G | C | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.293-64G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 2/21 | chr5 | 80055721 | ||||||
chr5:80056036
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
splice_region_variant&intron_variant | LOW | c.540+4G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056036 | ||||||
chr5:80056037
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
splice_region_variant&intron_variant | LOW | c.540+5G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056037 | ||||||
chr5:80056058
|
A | G | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.540+26A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056058 | ||||||
chr5:80056125
|
G | A | 3 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170 | 3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.540+93G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056125 | ||||||
chr5:80056354
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.540+322G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056354 | ||||||
chr5:80056397
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540+365A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056397 | ||||||
chr5:80056678
|
GAACTAGT others(80): Show |
G | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.540+652_540+738del others(87): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr5 | 80056678 | |||||
chr5:80056787
|
T | C | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.540+755T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056787 | ||||||
chr5:80056789
|
C | T | 2 | a0001c0003t0001g0238a0001c0003t0001g0239 | 2 | NA18975.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.540+757C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056789 | ||||||
chr5:80056904
|
T | C | 1 | a0001c0002t0001g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540+872T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80056904 | ||||||
chr5:80057044
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.540+1012G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057044 | ||||||
chr5:80057120
|
A | T | 3 | a0001c0002t0001g0033a0001c0002t0001g0304a0001c0002t0001g0313 | 4 | HG01074.hp2 HG01192.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-1086A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057120 | ||||||
chr5:80057163
|
G | A | 101 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(98): Show | 126 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.541-1043G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057163 | ||||||
chr5:80057262
|
C | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-944C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057262 | ||||||
chr5:80057294
|
T | G | 1 | a0001c0001t0001g0025 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.541-912T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057294 | ||||||
chr5:80057605
|
T | C | 8 | a0001c0003t0001g0001a0001c0003t0001g0030a0001c0003t0001g0229others(5): Show | 18 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-601T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057605 | ||||||
chr5:80057676
|
C | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-530C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057676 | ||||||
chr5:80057713
|
G | A | 1 | a0002c0004t0001g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.541-493G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057713 | ||||||
chr5:80057718
|
A | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-488A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057718 | ||||||
chr5:80057731
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-475G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057731 | ||||||
chr5:80057805
|
A | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-401A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057805 | ||||||
chr5:80057824
|
C | T | 196 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(193): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.541-382C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057824 | ||||||
chr5:80057895
|
C | T | 1 | a0001c0003t0001g0197 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.541-311C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80057895 | ||||||
chr5:80058012
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541-194A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058012 | ||||||
chr5:80058137
|
G | A | 1 | a0001c0003t0001g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.541-69G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058137 | ||||||
chr5:80058143
|
A | G | 1 | a0001c0002t0001g0035 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.541-63A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058143 | ||||||
chr5:80058179
|
C | A | 1 | a0005c0009t0001g0287 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.541-27C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 3/21 | chr5 | 80058179 | ||||||
chr5:80058324
|
C | T | 198 | a0001c0001t0001g0081a0001c0002t0001g0006a0001c0002t0001g0015others(195): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.649+10C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058324 | ||||||
chr5:80058361
|
A | G | 109 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(106): Show | 136 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.649+47A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058361 | ||||||
chr5:80058363
|
A | G | 1 | a0001c0003t0001g0244 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.649+49A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058363 | ||||||
chr5:80058391
|
C | G | 1 | a0001c0002t0001g0303 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.649+77C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058391 | ||||||
chr5:80058398
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.649+84T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058398 | ||||||
chr5:80058470
|
A | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.649+156A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058470 | ||||||
chr5:80058544
|
A | AT | 105 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(102): Show | 132 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.650-156dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr5 | 80058544 | |||||
chr5:80058582
|
A | G | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.650-126A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 4/21 | chr5 | 80058582 | ||||||
chr5:80058824
|
C | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.732+34C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80058824 | ||||||
chr5:80058879
|
C | T | 195 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0032others(192): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.732+89C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80058879 | ||||||
chr5:80058905
|
C | T | 85 | a0001c0001t0001g0075a0001c0002t0001g0006a0001c0002t0001g0015others(82): Show | 96 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.732+115C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80058905 | ||||||
chr5:80058972
|
GTGA | G | 3 | a0001c0002t0001g0033a0001c0002t0001g0304a0001c0002t0001g0313 | 4 | HG01074.hp2 HG01192.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+186_732+188del others(3): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 80058972 | |||||
chr5:80059025
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.732+235C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059025 | ||||||
chr5:80059069
|
T | C | 196 | a0001c0001t0001g0136a0001c0002t0001g0006a0001c0002t0001g0015others(193): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.732+279T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059069 | ||||||
chr5:80059172
|
A | G | 3 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143 | 3 | HG00642.hp2 HG01167.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.733-268A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059172 | ||||||
chr5:80059199
|
G | A | 196 | a0001c0001t0001g0136a0001c0002t0001g0006a0001c0002t0001g0015others(193): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.733-241G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059199 | ||||||
chr5:80059315
|
C | G | 1 | a0001c0001t0001g0151 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.733-125C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059315 | ||||||
chr5:80059327
|
C | CA | 5 | a0001c0001t0001g0098a0001c0001t0001g0126a0001c0001t0001g0149others(2): Show | 7 | HG00280.hp2 HG02027.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.733-94dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 80059327 | |||||
chr5:80059327
|
CA | C | 108 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0096others(105): Show | 133 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.733-94delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr5 | 80059327 | |||||
chr5:80059341
|
A | G | 1 | a0004c0008t0001g0014 | 3 | HG01243.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.733-99A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059341 | ||||||
chr5:80059369
|
T | A | 198 | a0001c0001t0001g0136a0001c0002t0001g0006a0001c0002t0001g0015others(195): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.733-71T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 5/21 | chr5 | 80059369 | ||||||
chr5:80059555
|
G | A | 1 | a0002c0004t0001g0227 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.784+64G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059555 | ||||||
chr5:80059572
|
C | T | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.784+81C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059572 | ||||||
chr5:80059648
|
C | T | 89 | a0001c0001t0001g0136a0001c0002t0001g0006a0001c0002t0001g0015others(86): Show | 100 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.785-55C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059648 | ||||||
chr5:80059667
|
C | T | 1 | a0001c0002t0001g0270 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.785-36C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 6/21 | chr5 | 80059667 | ||||||
chr5:80060001
|
T | G | 1 | a0001c0002t0003g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.987+96T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060001 | ||||||
chr5:80060106
|
T | C | 3 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170 | 3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.987+201T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060106 | ||||||
chr5:80060169
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.987+264C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060169 | ||||||
chr5:80060337
|
C | T | 2 | a0001c0010t0001g0251a0001c0010t0001g0252 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.987+432C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060337 | ||||||
chr5:80060424
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.987+519A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060424 | ||||||
chr5:80060543
|
T | G | 1 | a0002c0004t0001g0177 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.987+638T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060543 | ||||||
chr5:80060759
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.987+854A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060759 | ||||||
chr5:80060762
|
CA | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0046others(2): Show | 6 | HG03130.hp1 HG03139.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+866delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr5 | 80060762 | |||||
chr5:80060808
|
T | C | 1 | a0001c0003t0001g0230 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.988-887T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060808 | ||||||
chr5:80060997
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.988-698G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80060997 | ||||||
chr5:80061039
|
T | C | 1 | a0001c0002t0001g0318 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.988-656T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061039 | ||||||
chr5:80061294
|
G | A | 8 | a0002c0005t0001g0012a0002c0005t0001g0165a0002c0005t0001g0192others(5): Show | 10 | HG00408.hp1 NA18942.hp1 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-401G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061294 | ||||||
chr5:80061323
|
C | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG02027.hp1 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-372C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061323 | ||||||
chr5:80061350
|
C | T | 1 | a0001c0002t0001g0311 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.988-345C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061350 | ||||||
chr5:80061361
|
T | C | 1 | a0001c0003t0001g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.988-334T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061361 | ||||||
chr5:80061515
|
C | G | 1 | a0002c0004t0001g0179 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.988-180C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061515 | ||||||
chr5:80061613
|
A | C | 1 | a0001c0002t0001g0270 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.988-82A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 7/21 | chr5 | 80061613 | ||||||
chr5:80062045
|
A | C | 1 | a0001c0003t0001g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1125+213A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062045 | ||||||
chr5:80062150
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1125+318T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062150 | ||||||
chr5:80062491
|
A | C | 1 | a0002c0004t0001g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+659A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062491 | ||||||
chr5:80062495
|
T | C | 1 | a0002c0004t0001g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+663T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062495 | ||||||
chr5:80062496
|
T | A | 1 | a0002c0004t0001g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+664T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062496 | ||||||
chr5:80062498
|
C | A | 1 | a0002c0004t0001g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+666C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062498 | ||||||
chr5:80062499
|
C | G | 38 | a0001c0003t0001g0004a0001c0003t0001g0011a0001c0003t0001g0029others(35): Show | 45 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1125+667C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062499 | ||||||
chr5:80062503
|
C | A | 1 | a0002c0004t0001g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+671C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062503 | ||||||
chr5:80062506
|
C | T | 1 | a0002c0004t0001g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1125+674C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062506 | ||||||
chr5:80062610
|
G | A | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1125+778G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062610 | ||||||
chr5:80062798
|
C | T | 2 | a0001c0010t0001g0251a0001c0010t0001g0252 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1125+966C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062798 | ||||||
chr5:80062804
|
G | A | 3 | a0001c0003t0001g0241a0001c0003t0001g0242a0001c0003t0001g0243 | 3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1125+972G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062804 | ||||||
chr5:80062837
|
A | G | 1 | a0001c0003t0001g0237 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1125+1005A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062837 | ||||||
chr5:80062837
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1125+1005A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80062837 | ||||||
chr5:80063046
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1125+1214G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063046 | ||||||
chr5:80063403
|
T | TTAAG | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+1573_1125+157 others(8): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr5 | 80063403 | |||||
chr5:80063419
|
G | A | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+1587G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063419 | ||||||
chr5:80063504
|
G | T | 1 | a0002c0004t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1125+1672G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063504 | ||||||
chr5:80063665
|
A | G | 8 | a0001c0002t0001g0033a0001c0002t0001g0263a0001c0002t0001g0264others(5): Show | 11 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1126-1744A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063665 | ||||||
chr5:80063782
|
G | C | 1 | a0001c0003t0001g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1126-1627G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80063782 | ||||||
chr5:80064215
|
A | G | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1126-1194A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064215 | ||||||
chr5:80064351
|
T | C | 197 | a0001c0001t0001g0136a0001c0002t0001g0006a0001c0002t0001g0015others(194): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1126-1058T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064351 | ||||||
chr5:80064352
|
G | A | 9 | a0001c0003t0001g0001a0001c0003t0001g0030a0001c0003t0001g0229others(6): Show | 19 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1126-1057G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064352 | ||||||
chr5:80064568
|
T | C | 1 | a0001c0002t0001g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1126-841T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064568 | ||||||
chr5:80064588
|
G | A | 2 | a0001c0003t0001g0041a0001c0003t0001g0042 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1126-821G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064588 | ||||||
chr5:80064635
|
G | T | 2 | a0001c0003t0001g0171a0001c0003t0001g0196 | 2 | NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1126-774G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064635 | ||||||
chr5:80064688
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0135 | 2 | HG02698.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1126-721T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064688 | ||||||
chr5:80064712
|
A | T | 44 | a0002c0004t0001g0010a0002c0004t0001g0013a0002c0004t0001g0028others(41): Show | 52 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1126-697A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80064712 | ||||||
chr5:80065003
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1126-406T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80065003 | ||||||
chr5:80065059
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1126-350T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 8/21 | chr5 | 80065059 | ||||||
chr5:80065579
|
CATAAT | C | 84 | a0001c0001t0001g0136a0001c0002t0001g0006a0001c0002t0001g0015others(81): Show | 95 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1194+106_1194+110d others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80065579 | |||||
chr5:80065589
|
T | A | 1 | a0007c0014t0001g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1194+112T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80065589 | ||||||
chr5:80065665
|
T | C | 17 | a0001c0003t0001g0173a0001c0003t0006g0172a0002c0004t0001g0199others(14): Show | 21 | HG00408.hp1 NA18942.hp1 NA18947.hp2 others(18): Show |
intron_variant | MODIFIER | c.1194+188T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80065665 | ||||||
chr5:80066019
|
C | T | 2 | a0001c0001t0001g0136a0001c0002t0001g0316 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1194+542C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066019 | ||||||
chr5:80066027
|
G | A | 1 | a0001c0003t0001g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1194+550G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066027 | ||||||
chr5:80066031
|
C | T | 38 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1194+554C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066031 | ||||||
chr5:80066050
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1194+573G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066050 | ||||||
chr5:80066093
|
T | C | 7 | a0001c0002t0001g0033a0001c0002t0001g0263a0001c0002t0001g0264others(4): Show | 10 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+616T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066093 | ||||||
chr5:80066094
|
C | CA | 18 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 19 | HG01261.hp2 HG01891.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1194+638dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80066094 | |||||
chr5:80066094
|
C | CAA | 9 | a0001c0002t0001g0259a0001c0002t0001g0270a0001c0002t0001g0275others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1194+637_1194+638d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80066094 | |||||
chr5:80066094
|
CA | C | 95 | a0001c0001t0001g0059a0001c0001t0001g0104a0001c0002t0001g0257others(92): Show | 120 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1194+638delA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80066094 | |||||
chr5:80066095
|
A | C | 1 | a0004c0008t0001g0269 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1194+618A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066095 | ||||||
chr5:80066349
|
T | C | 4 | a0001c0002t0001g0275a0001c0002t0001g0276a0001c0002t0001g0277others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+872T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066349 | ||||||
chr5:80066408
|
C | A | 1 | a0001c0001t0001g0085 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1194+931C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066408 | ||||||
chr5:80066420
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1194+943A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066420 | ||||||
chr5:80066477
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1194+1000T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066477 | ||||||
chr5:80066626
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1194+1149G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066626 | ||||||
chr5:80066689
|
G | T | 2 | a0001c0002t0001g0263a0001c0002t0001g0264 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1194+1212G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066689 | ||||||
chr5:80066690
|
C | T | 1 | a0001c0002t0001g0301 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1194+1213C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066690 | ||||||
chr5:80066727
|
G | A | 9 | a0001c0002t0001g0259a0001c0002t0001g0270a0001c0002t0001g0275others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195-1246G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066727 | ||||||
chr5:80066756
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1195-1217T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066756 | ||||||
chr5:80066789
|
G | C | 45 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(42): Show | 62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1195-1184G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066789 | ||||||
chr5:80066858
|
G | A | 37 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(34): Show | 38 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1195-1115G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066858 | ||||||
chr5:80066895
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1195-1078A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066895 | ||||||
chr5:80066926
|
G | T | 1 | a0001c0002t0001g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1195-1047G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80066926 | ||||||
chr5:80067039
|
G | A | 2 | a0001c0003t0001g0041a0001c0003t0001g0042 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1195-934G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067039 | ||||||
chr5:80067234
|
T | TA | 38 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1195-737dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80067234 | |||||
chr5:80067254
|
C | T | 2 | a0001c0002t0001g0160a0001c0002t0001g0161 | 2 | HG01358.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1195-719C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067254 | ||||||
chr5:80067388
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1195-585T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067388 | ||||||
chr5:80067450
|
G | A | 98 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(95): Show | 123 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1195-523G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067450 | ||||||
chr5:80067480
|
G | T | 1 | a0001c0003t0001g0315 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1195-493G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067480 | ||||||
chr5:80067501
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0253 | 3 | HG01891.hp2 HG02145.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1195-472C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067501 | ||||||
chr5:80067785
|
C | CA | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1195-187dupA | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr5 | 80067785 | |||||
chr5:80067936
|
A | C | 2 | a0001c0003t0001g0030a0001c0003t0001g0234 | 3 | HG00738.hp1 HG01069.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1195-37A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067936 | ||||||
chr5:80067968
|
T | C | 1 | a0001c0003t0001g0218 | 1 | NA19064.hp1 | splice_region_variant&intron_variant | LOW | c.1195-5T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 9/21 | chr5 | 80067968 | ||||||
chr5:80068200
|
G | A | 1 | a0002c0004t0001g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1347+75G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068200 | ||||||
chr5:80068492
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1347+367T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068492 | ||||||
chr5:80068577
|
T | C | 38 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1347+452T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068577 | ||||||
chr5:80068595
|
G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0047a0008c0015t0001g0022 | 3 | HG01884.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1347+470G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068595 | ||||||
chr5:80068728
|
G | A | 1 | a0001c0003t0001g0230 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1347+603G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068728 | ||||||
chr5:80068751
|
C | T | 2 | a0001c0002t0001g0160a0001c0002t0001g0161 | 2 | HG01358.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1347+626C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068751 | ||||||
chr5:80068853
|
A | C | 38 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1347+728A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80068853 | ||||||
chr5:80069186
|
A | G | 106 | a0001c0003t0001g0001a0001c0003t0001g0004a0001c0003t0001g0011others(103): Show | 133 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1347+1061A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069186 | ||||||
chr5:80069224
|
T | A | 1 | a0001c0003t0001g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1348-1082T>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069224 | ||||||
chr5:80069262
|
A | G | 38 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(35): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1348-1044A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069262 | ||||||
chr5:80069493
|
T | C | 1 | a0001c0002t0001g0143 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1348-813T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069493 | ||||||
chr5:80069727
|
C | G | 3 | a0005c0009t0001g0287a0005c0009t0001g0300a0005c0009t0001g0308 | 3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1348-579C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069727 | ||||||
chr5:80069734
|
G | T | 3 | a0002c0004t0001g0183a0002c0004t0001g0186a0002c0004t0001g0187 | 3 | NA18940.hp2 NA19002.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1348-572G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069734 | ||||||
chr5:80069802
|
C | T | 1 | a0002c0004t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1348-504C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069802 | ||||||
chr5:80069836
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1348-470G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069836 | ||||||
chr5:80069848
|
G | A | 2 | a0001c0003t0001g0229a0001c0003t0001g0231 | 2 | HG01070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1348-458G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80069848 | ||||||
chr5:80070003
|
C | T | 2 | a0001c0003t0001g0041a0001c0003t0001g0042 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1348-303C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070003 | ||||||
chr5:80070121
|
C | CT | 238 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(235): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1348-182dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr5 | 80070121 | |||||
chr5:80070153
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1348-153G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070153 | ||||||
chr5:80070257
|
T | C | 104 | a0001c0001t0001g0136a0001c0001t0001g0145a0001c0002t0001g0259others(101): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1348-49T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070257 | ||||||
chr5:80070303
|
C | T | 2 | a0001c0010t0001g0251a0001c0010t0001g0252 | 2 | HG02723.hp1 HG02965.hp1 |
splice_region_variant&intron_variant | LOW | c.1348-3C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 10/21 | chr5 | 80070303 | ||||||
chr5:80070426
|
T | G | 103 | a0001c0001t0001g0062a0001c0002t0001g0259a0001c0002t0001g0270others(100): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1452+16T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 11/21 | chr5 | 80070426 | ||||||
chr5:80070790
|
C | G | 1 | a0001c0002t0001g0303 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1560+40C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070790 | ||||||
chr5:80070809
|
G | A | 3 | a0001c0002t0001g0033a0001c0002t0001g0304a0001c0002t0001g0313 | 4 | HG01074.hp2 HG01192.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1560+59G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070809 | ||||||
chr5:80070910
|
T | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(28): Show | 32 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1561-111T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070910 | ||||||
chr5:80070936
|
G | A | 1 | a0002c0004t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1561-85G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 12/21 | chr5 | 80070936 | ||||||
chr5:80071274
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1720+94G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071274 | ||||||
chr5:80071285
|
G | A | 4 | a0001c0003t0001g0041a0001c0003t0001g0042a0002c0004t0001g0013others(1): Show | 6 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+105G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071285 | ||||||
chr5:80071655
|
T | TAC | 19 | a0001c0001t0001g0048a0001c0001t0001g0105a0001c0001t0001g0106others(16): Show | 22 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1720+505_1720+506d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80071655 | |||||
chr5:80071655
|
TAC | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(208): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1720+505_1720+506d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80071655 | |||||
chr5:80071655
|
TACAC | T | 25 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0219others(22): Show | 27 | HG00609.hp1 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1720+503_1720+506d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80071655 | |||||
chr5:80071659
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1720+479C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071659 | ||||||
chr5:80071745
|
A | T | 1 | a0001c0002t0001g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1721-533A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071745 | ||||||
chr5:80071903
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1721-375G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80071903 | ||||||
chr5:80072193
|
T | C | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(324): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1721-85T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | chr5 | 80072193 | ||||||
chr5:80072225
|
TAGA | T | 94 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0094others(91): Show | 116 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.1721-47_1721-45del others(3): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr5 | 80072225 | |||||
chr5:80072522
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1839+126G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80072522 | ||||||
chr5:80072569
|
A | G | 129 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(126): Show | 144 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1839+173A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80072569 | ||||||
chr5:80072993
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1840-282C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80072993 | ||||||
chr5:80073155
|
C | T | 1 | a0001c0003t0001g0168 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1840-120C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80073155 | ||||||
chr5:80073226
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1840-49C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 14/21 | chr5 | 80073226 | ||||||
chr5:80073389
|
TG | T | 15 | a0001c0001t0001g0062a0001c0002t0001g0033a0001c0002t0001g0263others(12): Show | 28 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1892+63delG | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073389 | ||||||
chr5:80073390
|
G | T | 120 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(117): Show | 132 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1892+63G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073390 | ||||||
chr5:80073472
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1892+145T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073472 | ||||||
chr5:80073586
|
A | G | 3 | a0001c0001t0001g0022a0001c0001t0001g0047a0008c0015t0001g0022 | 3 | HG01884.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1892+259A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073586 | ||||||
chr5:80073635
|
C | T | 2 | a0001c0003t0001g0323a0001c0003t0001g0324 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1892+308C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073635 | ||||||
chr5:80073856
|
T | C | 8 | a0002c0005t0001g0012a0002c0005t0001g0165a0002c0005t0001g0192others(5): Show | 10 | NA18942.hp1 NA18974.hp1 NA18988.hp1 others(7): Show |
intron_variant | MODIFIER | c.1892+529T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073856 | ||||||
chr5:80073857
|
C | T | 1 | a0001c0002t0001g0259 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1892+530C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80073857 | ||||||
chr5:80074055
|
C | A | 13 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0060others(10): Show | 14 | HG01361.hp1 HG02698.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.1892+728C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074055 | ||||||
chr5:80074067
|
G | A | 4 | a0001c0001t0001g0136a0001c0002t0001g0316a0001c0010t0001g0251others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1892+740G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074067 | ||||||
chr5:80074301
|
C | T | 3 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143 | 3 | HG00642.hp2 HG01167.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1892+974C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074301 | ||||||
chr5:80074386
|
C | G | 1 | a0002c0004t0001g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1892+1059C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074386 | ||||||
chr5:80074424
|
G | T | 7 | a0001c0001t0001g0062a0001c0003t0001g0001a0001c0003t0001g0030others(4): Show | 17 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1892+1097G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074424 | ||||||
chr5:80074521
|
C | T | 236 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(233): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1892+1194C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074521 | ||||||
chr5:80074615
|
GCTCT | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0044 | 3 | HG02615.hp2 NA18942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1892+1297_1892+130 others(8): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074615 | |||||
chr5:80074626
|
C | CT | 8 | a0001c0001t0001g0077a0001c0001t0001g0114a0001c0001t0001g0120others(5): Show | 10 | HG01243.hp2 HG02055.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.1892+1314dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | |||||
chr5:80074626
|
C | CTT | 33 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0058others(30): Show | 36 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1892+1313_1892+131 others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | |||||
chr5:80074626
|
C | CTTT | 6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG00597.hp1 HG02451.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.1892+1312_1892+131 others(7): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | |||||
chr5:80074626
|
CT | C | 12 | a0001c0001t0001g0062a0001c0001t0001g0088a0001c0001t0001g0147others(9): Show | 22 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1892+1314delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074626 | |||||
chr5:80074833
|
G | A | 1 | a0001c0002t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1892+1506G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074833 | ||||||
chr5:80074931
|
C | T | 1 | a0001c0002t0001g0158 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1892+1604C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074931 | ||||||
chr5:80074938
|
TGTCCCAG others(7): Show |
T | 2 | a0001c0010t0001g0251a0001c0010t0001g0252 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1892+1620_1892+163 others(18): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr5 | 80074938 | |||||
chr5:80074941
|
C | T | 1 | a0001c0003t0001g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1892+1614C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074941 | ||||||
chr5:80074952
|
G | A | 1 | a0001c0002t0001g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1892+1625G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80074952 | ||||||
chr5:80075036
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1892+1709A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075036 | ||||||
chr5:80075043
|
A | G | 133 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(130): Show | 152 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.1892+1716A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075043 | ||||||
chr5:80075118
|
A | G | 1 | a0001c0002t0001g0313 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1893-1737A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075118 | ||||||
chr5:80075382
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1893-1473G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075382 | ||||||
chr5:80075424
|
C | T | 2 | a0001c0010t0001g0251a0001c0010t0001g0252 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1893-1431C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075424 | ||||||
chr5:80075595
|
A | G | 1 | a0001c0003t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1893-1260A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075595 | ||||||
chr5:80075900
|
A | G | 1 | a0002c0004t0001g0322 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1893-955A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80075900 | ||||||
chr5:80076032
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1893-823T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076032 | ||||||
chr5:80076228
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1893-627C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076228 | ||||||
chr5:80076584
|
C | T | 229 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(226): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1893-271C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076584 | ||||||
chr5:80076608
|
T | C | 1 | a0001c0002t0001g0318 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1893-247T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076608 | ||||||
chr5:80076645
|
G | A | 2 | a0002c0004t0001g0013a0006c0011t0001g0222 | 4 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-210G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 15/21 | chr5 | 80076645 | ||||||
chr5:80077132
|
C | T | 3 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170 | 3 | HG02922.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2086+84C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077132 | ||||||
chr5:80077212
|
A | G | 2 | a0001c0003t0001g0209a0001c0003t0001g0210 | 2 | HG00544.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2086+164A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077212 | ||||||
chr5:80077287
|
G | A | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2086+239G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077287 | ||||||
chr5:80077461
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2086+413A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077461 | ||||||
chr5:80077598
|
G | A | 1 | a0002c0004t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2087-451G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077598 | ||||||
chr5:80077617
|
C | T | 11 | a0001c0003t0001g0029a0001c0003t0001g0168a0001c0003t0001g0174others(8): Show | 12 | HG00544.hp2 NA18948.hp1 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.2087-432C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077617 | ||||||
chr5:80077640
|
G | C | 35 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0050others(32): Show | 36 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2087-409G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077640 | ||||||
chr5:80077698
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2087-351G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077698 | ||||||
chr5:80077960
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2087-89T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077960 | ||||||
chr5:80077980
|
C | T | 137 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(134): Show | 164 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.2087-69C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077980 | ||||||
chr5:80077989
|
C | A | 2 | a0001c0003t0001g0041a0001c0003t0001g0042 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2087-60C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80077989 | ||||||
chr5:80078012
|
C | T | 1 | a0001c0003t0001g0224 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2087-37C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 16/21 | chr5 | 80078012 | ||||||
chr5:80078342
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0078 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2265+115G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078342 | ||||||
chr5:80078468
|
C | T | 2 | a0001c0003t0001g0041a0001c0003t0001g0042 | 2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2265+241C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078468 | ||||||
chr5:80078556
|
C | T | 41 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0003t0001g0004others(38): Show | 50 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2265+329C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078556 | ||||||
chr5:80078650
|
T | C | 1 | a0001c0003t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2266-271T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078650 | ||||||
chr5:80078658
|
A | T | 1 | a0001c0002t0001g0258 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2266-263A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078658 | ||||||
chr5:80078765
|
A | C | 1 | a0002c0004t0001g0028 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2266-156A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078765 | ||||||
chr5:80078784
|
AT | A | 133 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(130): Show | 160 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.2266-134delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr5 | 80078784 | |||||
chr5:80078858
|
A | T | 1 | a0001c0002t0001g0309 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2266-63A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 17/21 | chr5 | 80078858 | ||||||
chr5:80079435
|
A | C | 2 | a0001c0001t0001g0136a0001c0002t0001g0316 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2511+177A>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079435 | ||||||
chr5:80079691
|
CATGGAAT others(5): Show |
C | 1 | a0001c0003t0001g0213 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2512-206_2512-195d others(14): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 80079691 | |||||
chr5:80079752
|
T | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0072others(11): Show | 16 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.2512-153T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079752 | ||||||
chr5:80079772
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2512-133T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079772 | ||||||
chr5:80079868
|
T | TGTCCTGT others(4): Show |
1 | a0001c0003t0001g0213 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2512-36_2512-26dup others(11): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr5 | 80079868 | |||||
chr5:80079889
|
T | C | 1 | a0001c0002t0001g0278 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2512-16T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079889 | ||||||
chr5:80079901
|
G | C | 135 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(132): Show | 162 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(159): Show |
splice_region_variant&intron_variant | LOW | c.2512-4G>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 19/21 | chr5 | 80079901 | ||||||
chr5:80080112
|
G | A | 1 | a0001c0003t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2684+35G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080112 | ||||||
chr5:80080128
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2684+51C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080128 | ||||||
chr5:80080321
|
G | A | 2 | a0001c0001t0001g0136a0001c0002t0001g0316 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2684+244G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080321 | ||||||
chr5:80080408
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0072others(10): Show | 15 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.2684+331G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080408 | ||||||
chr5:80080509
|
TGCA | T | 234 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(231): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.2684+436_2684+438d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080509 | |||||
chr5:80080565
|
A | G | 235 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(232): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2684+488A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080565 | ||||||
chr5:80080577
|
A | ATTTTTTT others(7): Show |
1 | a0002c0004t0001g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2684+501_2684+502i others(16): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080577 | |||||
chr5:80080579
|
C | CT | 6 | a0001c0001t0001g0065a0001c0001t0001g0091a0001c0001t0001g0253others(3): Show | 7 | HG01070.hp2 HG01952.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.2684+527dupT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTT | 5 | a0001c0001t0001g0024a0001c0001t0001g0148a0001c0001t0001g0152others(2): Show | 6 | HG00673.hp1 HG02074.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2684+525_2684+527d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(4): Show |
1 | a0005c0009t0001g0287 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2684+517_2684+527d others(13): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(6): Show |
20 | a0001c0002t0001g0270a0001c0002t0001g0275a0001c0003t0001g0229others(17): Show | 23 | HG00099.hp2 HG01070.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2684+515_2684+527d others(15): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(7): Show |
27 | a0001c0001t0001g0108a0001c0002t0001g0276a0001c0002t0001g0279others(24): Show | 33 | HG00609.hp2 HG00642.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.2684+514_2684+527d others(16): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(8): Show |
17 | a0001c0002t0001g0247a0001c0002t0001g0277a0001c0002t0001g0280others(14): Show | 19 | HG00140.hp1 HG00408.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2684+513_2684+527d others(17): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(9): Show |
15 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0002t0001g0306others(12): Show | 16 | HG00140.hp2 HG00673.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2684+512_2684+527d others(18): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(10): Show |
11 | a0001c0002t0001g0157a0001c0002t0001g0158a0001c0002t0001g0161others(8): Show | 11 | HG00609.hp1 HG00741.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2684+511_2684+527d others(19): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(11): Show |
12 | a0001c0002t0001g0139a0001c0002t0001g0141a0001c0002t0001g0155others(9): Show | 12 | HG01167.hp2 HG01952.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.2684+510_2684+527d others(20): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(12): Show |
14 | a0001c0002t0001g0006a0001c0002t0001g0142a0001c0002t0001g0143others(11): Show | 19 | HG00544.hp2 HG00642.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2684+509_2684+527d others(21): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(13): Show |
15 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0002t0001g0015others(12): Show | 18 | HG00597.hp2 HG01891.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.2684+508_2684+527d others(22): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(14): Show |
13 | a0001c0002t0001g0034a0001c0002t0001g0140a0001c0002t0001g0258others(10): Show | 15 | HG00733.hp2 HG01099.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.2684+507_2684+527d others(23): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0054a0001c0002t0001g0311a0001c0002t0001g0312others(1): Show | 5 | HG02071.hp2 HG03704.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.2684+506_2684+527d others(24): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0001g0056a0001c0002t0001g0266a0002c0007t0002g0163 | 3 | HG00597.hp1 HG02559.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2684+505_2684+527d others(25): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0050a0001c0002t0001g0283a0001c0002t0001g0299 | 3 | HG02040.hp2 HG02615.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2684+504_2684+527d others(26): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0058a0001c0003t0001g0212 | 2 | NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2684+503_2684+527d others(27): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(19): Show |
4 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0094others(1): Show | 4 | HG02056.hp2 HG02155.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.2684+527_2684+528i others(28): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(20): Show |
5 | a0001c0001t0001g0049a0001c0001t0001g0106a0001c0001t0001g0109others(2): Show | 5 | HG02129.hp2 HG02735.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2684+527_2684+528i others(29): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0069a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG00621.hp2 NA18994.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2684+527_2684+528i others(30): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(22): Show |
6 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0001g0107others(3): Show | 6 | HG01123.hp2 HG02818.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+527_2684+528i others(31): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(23): Show |
3 | a0001c0001t0001g0110a0001c0001t0001g0125a0001c0003t0001g0174 | 3 | HG02300.hp1 NA18948.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2684+527_2684+528i others(32): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0154 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2684+527_2684+528i others(35): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0126 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2684+527_2684+528i others(36): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
C | T | 1 | a0002c0004t0001g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2684+502C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080579 | ||||||
chr5:80080579
|
CT | C | 10 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0084others(7): Show | 10 | HG02132.hp1 HG03486.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.2684+527delT | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080579
|
CTT | C | 13 | a0001c0002t0001g0033a0001c0002t0001g0263a0001c0002t0001g0264others(10): Show | 26 | HG00323.hp2 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2684+526_2684+527d others(4): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080579 | |||||
chr5:80080588
|
T | TTTTTTTT others(10): Show |
2 | a0001c0002t0001g0285a0001c0002t0001g0294 | 2 | HG00438.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.2684+527_2684+528i others(19): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80080588 | |||||
chr5:80080691
|
A | T | 127 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(124): Show | 144 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.2684+614A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080691 | ||||||
chr5:80080735
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2684+658C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080735 | ||||||
chr5:80080736
|
G | A | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2684+659G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080736 | ||||||
chr5:80080743
|
C | T | 1 | a0001c0002t0001g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2684+666C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080743 | ||||||
chr5:80080744
|
G | A | 9 | a0001c0003t0001g0144a0001c0003t0001g0169a0001c0003t0001g0170others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2684+667G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080744 | ||||||
chr5:80080993
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2684+916T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80080993 | ||||||
chr5:80081082
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2684+1005T>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081082 | ||||||
chr5:80081140
|
G | A | 1 | a0001c0003t0001g0196 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2684+1063G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081140 | ||||||
chr5:80081211
|
A | T | 1 | a0001c0002t0001g0285 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2684+1134A>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081211 | ||||||
chr5:80081308
|
C | T | 3 | a0001c0003t0001g0241a0001c0003t0001g0242a0001c0003t0001g0243 | 3 | HG01884.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2685-1098C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081308 | ||||||
chr5:80081347
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2685-1059C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081347 | ||||||
chr5:80081410
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2685-996G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081410 | ||||||
chr5:80081426
|
A | G | 48 | a0001c0002t0001g0006a0001c0002t0001g0015a0001c0002t0001g0034others(45): Show | 55 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.2685-980A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081426 | ||||||
chr5:80081532
|
C | T | 1 | a0002c0004t0001g0185 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2685-874C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081532 | ||||||
chr5:80081750
|
T | C | 1 | a0001c0003t0001g0324 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2685-656T>C | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80081750 | ||||||
chr5:80082018
|
G | GGTA | 4 | a0001c0003t0001g0323a0001c0003t0001g0324a0002c0004t0001g0013others(1): Show | 6 | HG01891.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2685-387_2685-385d others(5): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr5 | 80082018 | |||||
chr5:80082033
|
C | T | 1 | a0001c0002t0001g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2685-373C>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082033 | ||||||
chr5:80082077
|
G | T | 235 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(232): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2685-329G>T | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082077 | ||||||
chr5:80082114
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2685-292A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082114 | ||||||
chr5:80082204
|
A | G | 3 | a0001c0002t0001g0275a0001c0002t0001g0277a0001c0002t0001g0280 | 3 | HG00099.hp2 HG00140.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.2685-202A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082204 | ||||||
chr5:80082247
|
C | G | 235 | a0001c0001t0001g0024a0001c0001t0001g0044a0001c0001t0001g0049others(232): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.2685-159C>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082247 | ||||||
chr5:80082311
|
A | G | 2 | a0001c0001t0001g0059a0001c0003t0001g0211 | 2 | HG00558.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.2685-95A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 20/21 | chr5 | 80082311 | ||||||
chr5:80082624
|
T | TC | 85 | a0001c0001t0001g0094a0001c0002t0001g0006a0001c0002t0001g0015others(82): Show | 98 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.2824+86dupC | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr5 | 80082624 | |||||
chr5:80082686
|
C | A | 1 | a0002c0004t0001g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2824+141C>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80082686 | ||||||
chr5:80082705
|
A | G | 292 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(289): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.2824+160A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80082705 | ||||||
chr5:80082812
|
A | G | 2 | a0001c0003t0001g0169a0001c0003t0001g0170 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2824+267A>G | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80082812 | ||||||
chr5:80082839
|
T | TAATC | 3 | a0005c0009t0001g0287a0005c0009t0001g0300a0005c0009t0001g0308 | 3 | HG02257.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2825-239_2825-236d others(6): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr5 | 80082839 | |||||
chr5:80082960
|
TGCGGGGC others(7): Show |
T | 94 | a0001c0001t0001g0044a0001c0001t0001g0094a0001c0002t0001g0006others(91): Show | 110 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.2825-114_2825-101d others(16): Show |
THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr5 | 80082960 | |||||
chr5:80083002
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2825-78G>A | THBS4 | ENSG00000113296.14 | transcript | ENST00000350881.6 | protein_coding | 21/21 | chr5 | 80083002 |