geneid | 4090 |
---|---|
ensemblid | ENSG00000113658.18 |
hgncid | 6771 |
symbol | SMAD5 |
name | SMAD family member 5 |
refseq_nuc | NM_005903.7 |
refseq_prot | NP_005894.3 |
ensembl_nuc | ENST00000545279.6 |
ensembl_prot | ENSP00000441954.2 |
mane_status | MANE Select |
chr | chr5 |
start | 136132845 |
end | 136182733 |
strand | + |
ver | v1.2 |
region | chr5:136132845-136182733 |
region5000 | chr5:136127845-136187733 |
regionname0 | SMAD5_chr5_136132845_136182733 |
regionname5000 | SMAD5_chr5_136127845_136187733 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 465 | 294 | 80 | 46 | 132 | 14 | 20 | 98 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1398 | 291 | 80 | 43 | 132 | 14 | 20 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
c0002 | 0/0 | 1398 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
c0003 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 5616 | 117 | 19 | 18 | 61 | 5 | 12 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0002 | 0/0 | 5620 | 60 | 10 | 5 | 36 | 4 | 5 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0003 | 0/0 | 5619 | 43 | 14 | 12 | 12 | 2 | 3 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0004 | 0/0 | 5619 | 8 | 6 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0005 | 0/0 | 5620 | 7 | 5 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0006 | 0/0 | 5620 | 7 | 0 | 0 | 7 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0007 | 0/0 | 5619 | 6 | 6 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0008 | 0/0 | 5616 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0009 | 0/0 | 5616 | 4 | 0 | 3 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0010 | 0/0 | 5616 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0011 | 0/0 | 5621 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0012 | 0/0 | 5615 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0013 | 0/0 | 5619 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0014 | 0/0 | 5617 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0015 | 0/0 | 5619 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0016 | 0/0 | 5617 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0017 | 0/0 | 5619 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0018 | 0/0 | 5619 | 2 | 0 | 0 | 0 | 2 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0019 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0020 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0021 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0022 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0023 | 0/0 | 5616 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0024 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0025 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0026 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0027 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0028 | 0/0 | 5620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0029 | 0/0 | 5617 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0030 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0031 | 0/0 | 5620 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
t0032 | 0/0 | 5617 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0012 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0034 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1398 | 291 | 80 | 43 | 132 | 14 | 20 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0002 | 0/0 | 1398 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0003 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7013 | 115 | 19 | 16 | 61 | 5 | 12 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0002 | 0/0 | 7017 | 60 | 10 | 5 | 36 | 4 | 5 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0003 | 0/0 | 7016 | 43 | 14 | 12 | 12 | 2 | 3 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0004 | 0/0 | 7016 | 8 | 6 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0005 | 0/0 | 7017 | 7 | 5 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0006 | 0/0 | 7017 | 7 | 0 | 0 | 7 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0007 | 0/0 | 7016 | 6 | 6 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0008 | 0/0 | 7013 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0009 | 0/0 | 7013 | 3 | 0 | 2 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0010 | 0/0 | 7013 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0011 | 0/0 | 7018 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0012 | 0/0 | 7012 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0013 | 0/0 | 7016 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0014 | 0/0 | 7014 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0015 | 0/0 | 7016 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0016 | 0/0 | 7014 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0017 | 0/0 | 7016 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0018 | 0/0 | 7016 | 2 | 0 | 0 | 0 | 2 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0019 | 0/0 | 7013 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0020 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0021 | 0/0 | 7013 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0022 | 0/0 | 7013 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0023 | 0/0 | 7013 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0024 | 0/0 | 7013 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0025 | 0/0 | 7017 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0026 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0027 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0028 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0029 | 0/0 | 7014 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0030 | 0/0 | 7016 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0031 | 0/0 | 7017 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0001t0032 | 0/0 | 7014 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0002t0001 | 0/0 | 7013 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
a0001c0003t0009 | 0/0 | 7013 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | copy fasta | chr5 | 136127845 | 136187733 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0034 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0007g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0010g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0011g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0012g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0012g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0014g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0014g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0015g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0015g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0016g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0017g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0017g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0018g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0019g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0020g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0021g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0022g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0023g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0024g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0025g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0026g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0027g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0028g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0029g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0030g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0031g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0032g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0003t0009g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0118 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0061 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0097 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | FIN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00323 | hp2 | a0001 | c0001 | t0009 | g0153 | EUR | FIN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0216 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00423 | hp2 | a0001 | c0001 | t0020 | g0123 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0217 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00609 | hp1 | a0001 | c0001 | t0019 | g0012 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00735 | hp2 | a0001 | c0001 | t0023 | g0219 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0135 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0139 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0133 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0079 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0159 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01258 | hp1 | a0001 | c0001 | t0009 | g0032 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01496 | hp2 | a0001 | c0001 | t0014 | g0136 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01516 | hp1 | a0001 | c0001 | t0018 | g0013 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01517 | hp1 | a0001 | c0001 | t0018 | g0013 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0190 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01934 | hp1 | a0001 | c0003 | t0009 | g0154 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02040 | hp2 | a0001 | c0001 | t0027 | g0122 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02155 | hp2 | a0001 | c0001 | t0006 | g0119 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02165 | hp1 | a0001 | c0001 | t0028 | g0066 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02451 | hp2 | a0001 | c0001 | t0029 | g0065 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0075 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0071 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0081 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02897 | hp1 | a0001 | c0001 | t0016 | g0080 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02970 | hp2 | a0001 | c0001 | t0024 | g0214 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0021 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03195 | hp1 | a0001 | c0001 | t0031 | g0108 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0067 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0078 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03516 | hp1 | a0001 | c0001 | t0032 | g0074 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03540 | hp1 | a0001 | c0001 | t0030 | g0001 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0137 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0021 | AFR | YRI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18939 | hp2 | a0001 | c0001 | t0011 | g0024 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18961 | hp1 | a0001 | c0001 | t0026 | g0007 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18964 | hp2 | a0001 | c0001 | t0008 | g0218 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18988 | hp1 | a0001 | c0001 | t0021 | g0164 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19030 | hp2 | a0001 | c0001 | t0025 | g0006 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19056 | hp1 | a0001 | c0001 | t0012 | g0038 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19068 | hp2 | a0001 | c0001 | t0012 | g0039 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19070 | hp2 | a0001 | c0001 | t0012 | g0037 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19084 | hp1 | a0001 | c0001 | t0011 | g0024 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | ASW | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ASW | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0048 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0072 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0158 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03471 | hp2 | a0001 | c0001 | t0017 | g0073 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA21309 | hp1 | a0001 | c0001 | t0022 | g0237 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0034 | REF | REF | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0184 | REF | REF | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136154066
|
T | C | 1 | a0001c0002 | 2 | HG01168.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.306T>C | p.His102His | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/8 | 668/7013 | 306/1398 | 102/465 | chr5 | 136154066 | ||
chr5:136174389
|
C | T | 1 | a0001c0003 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1011C>T | p.Tyr337Tyr | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/8 | 1373/7013 | 1011/1398 | 337/465 | chr5 | 136174389 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136132914
|
G | A | 1 | a0001c0001t0019 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-293G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/8 | 20847 | chr5 | 136132914 | |||||
chr5:136147866
|
G | A | 1 | a0001c0001t0020 | 1 | HG00423.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/8 | 5895 | chr5 | 136147866 | |||||
chr5:136153746
|
G | A | 2 | a0001c0001t0008a0001c0001t0021 | 5 | HG00423.hp1 HG00438.hp2 NA18964.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/8 | 15 | chr5 | 136153746 | |||||
chr5:136178162
|
T | A | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*682T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 682 | chr5 | 136178162 | |||||
chr5:136178234
|
T | C | 1 | a0001c0001t0022 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*754T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 754 | chr5 | 136178234 | |||||
chr5:136178367
|
A | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*887A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 887 | chr5 | 136178367 | |||||
chr5:136178528
|
A | G | 2 | a0001c0001t0003a0001c0001t0032 | 44 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1048A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1048 | chr5 | 136178528 | |||||
chr5:136178653
|
G | A | 2 | a0001c0001t0004a0001c0001t0025 | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1173G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1173 | chr5 | 136178653 | |||||
chr5:136178662
|
T | C | 1 | a0001c0001t0005 | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1182T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1182 | chr5 | 136178662 | |||||
chr5:136178801
|
T | A | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1321T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1321 | chr5 | 136178801 | |||||
chr5:136179045
|
T | A | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1565T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1565 | chr5 | 136179045 | |||||
chr5:136179054
|
A | G | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1574A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1574 | chr5 | 136179054 | |||||
chr5:136179114
|
C | T | 1 | a0001c0001t0031 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1634C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1634 | chr5 | 136179114 | |||||
chr5:136179190
|
G | T | 1 | a0001c0001t0017 | 2 | HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1710G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1710 | chr5 | 136179190 | |||||
chr5:136179268
|
T | C | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1788T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1788 | chr5 | 136179268 | |||||
chr5:136179440
|
T | C | 1 | a0001c0001t0012 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1960T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1960 | chr5 | 136179440 | |||||
chr5:136179468
|
G | GA | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(5): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1998dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1999 | INFO_REALIGN_3_PRIME | chr5 | 136179468 | ||||
chr5:136179480
|
C | T | 1 | a0001c0001t0024 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2000 | chr5 | 136179480 | |||||
chr5:136179500
|
T | G | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2020T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2020 | chr5 | 136179500 | |||||
chr5:136179504
|
A | G | 1 | a0001c0001t0031 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2024A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2024 | chr5 | 136179504 | |||||
chr5:136179651
|
CCTTAA | C | 1 | a0001c0001t0012 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2172_*2176delCTTA others(1): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2172 | chr5 | 136179651 | |||||
chr5:136179670
|
A | G | 1 | a0001c0001t0021 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2190A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2190 | chr5 | 136179670 | |||||
chr5:136179808
|
G | GA | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*2334dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2335 | INFO_REALIGN_3_PRIME | chr5 | 136179808 | ||||
chr5:136179823
|
A | G | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2343A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2343 | chr5 | 136179823 | |||||
chr5:136180020
|
A | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2540A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2540 | chr5 | 136180020 | |||||
chr5:136180050
|
T | C | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2570T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2570 | chr5 | 136180050 | |||||
chr5:136180268
|
T | C | 2 | a0001c0001t0009a0001c0003t0009 | 4 | HG00323.hp2 HG01071.hp1 HG01258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2788T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2788 | chr5 | 136180268 | |||||
chr5:136180287
|
T | G | 17 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2807T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2807 | chr5 | 136180287 | |||||
chr5:136180500
|
T | G | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*3020T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3020 | chr5 | 136180500 | |||||
chr5:136180515
|
T | C | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3035T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3035 | chr5 | 136180515 | |||||
chr5:136180594
|
G | A | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3114G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3114 | chr5 | 136180594 | |||||
chr5:136180798
|
G | T | 3 | a0001c0001t0006a0001c0001t0020a0001c0001t0028 | 9 | HG00423.hp2 HG02083.hp1 HG02129.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3318G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3318 | chr5 | 136180798 | |||||
chr5:136181019
|
A | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3539A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3539 | chr5 | 136181019 | |||||
chr5:136181047
|
A | G | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3567A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3567 | chr5 | 136181047 | |||||
chr5:136181069
|
A | C | 1 | a0001c0001t0027 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3589A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3589 | chr5 | 136181069 | |||||
chr5:136181148
|
T | C | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3668T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3668 | chr5 | 136181148 | |||||
chr5:136181231
|
A | G | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3751A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3751 | chr5 | 136181231 | |||||
chr5:136181462
|
T | C | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(19): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3982T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3982 | chr5 | 136181462 | |||||
chr5:136181519
|
C | T | 1 | a0001c0001t0012 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4039C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4039 | chr5 | 136181519 | |||||
chr5:136181544
|
C | T | 1 | a0001c0001t0010 | 3 | HG01243.hp1 HG01884.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4064C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4064 | chr5 | 136181544 | |||||
chr5:136181717
|
G | C | 1 | a0001c0001t0029 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4237G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4237 | chr5 | 136181717 | |||||
chr5:136181857
|
A | T | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4377A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4377 | chr5 | 136181857 | |||||
chr5:136182052
|
T | G | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(5): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*4572T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4572 | chr5 | 136182052 | |||||
chr5:136182123
|
G | A | 1 | a0001c0001t0018 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4643G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4643 | chr5 | 136182123 | |||||
chr5:136182140
|
C | T | 1 | a0001c0001t0023 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4660C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4660 | chr5 | 136182140 | |||||
chr5:136182169
|
A | G | 1 | a0001c0001t0028 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4689A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4689 | chr5 | 136182169 | |||||
chr5:136182233
|
G | GAA | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(12): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*4766_*4767dupAA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4768 | INFO_REALIGN_3_PRIME | chr5 | 136182233 | ||||
chr5:136182233
|
G | GAAA | 4 | a0001c0001t0005a0001c0001t0011a0001c0001t0012others(1): Show | 14 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4765_*4767dupAAA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4768 | INFO_REALIGN_3_PRIME | chr5 | 136182233 | ||||
chr5:136182276
|
T | A | 1 | a0001c0001t0018 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4796T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4796 | chr5 | 136182276 | |||||
chr5:136182481
|
G | T | 1 | a0001c0001t0030 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5001G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5001 | chr5 | 136182481 | |||||
chr5:136182519
|
C | G | 1 | a0001c0001t0026 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5039C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5039 | chr5 | 136182519 | |||||
chr5:136182554
|
G | T | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*5074G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5074 | chr5 | 136182554 | |||||
chr5:136182592
|
A | G | 1 | a0001c0001t0005 | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5112A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5112 | chr5 | 136182592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136133001
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+39T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133001 | ||||||
chr5:136133092
|
G | T | 1 | a0001c0001t0003g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-245+130G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133092 | ||||||
chr5:136133174
|
T | A | 1 | a0001c0001t0002g0035 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-245+212T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133174 | ||||||
chr5:136133177
|
C | G | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-245+215C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133177 | ||||||
chr5:136133404
|
C | T | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-245+442C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133404 | ||||||
chr5:136133435
|
G | A | 1 | a0001c0001t0009g0139 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-245+473G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133435 | ||||||
chr5:136133811
|
C | T | 62 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(59): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-245+849C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133811 | ||||||
chr5:136133831
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-245+869A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133831 | ||||||
chr5:136133838
|
T | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-245+876T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133838 | ||||||
chr5:136134037
|
T | TG | 21 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0030others(18): Show | 28 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-245+1091dupG | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | |||||
chr5:136134037
|
TG | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(30): Show | 40 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-245+1091delG | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | |||||
chr5:136134037
|
TGG | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0001g0142others(25): Show | 30 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-245+1090_-245+109 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | |||||
chr5:136134037
|
TGGG | T | 126 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0002g0007others(123): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.-245+1089_-245+109 others(7): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | |||||
chr5:136134042
|
G | C | 3 | a0001c0001t0001g0140a0001c0001t0016g0080a0001c0001t0016g0081 | 3 | HG02895.hp2 HG02897.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-245+1080G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134042 | ||||||
chr5:136134043
|
G | C | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | NA18947.hp1 NA18952.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-245+1081G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134043 | ||||||
chr5:136134048
|
G | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-245+1086G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134048 | ||||||
chr5:136134050
|
G | T | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-245+1088G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134050 | ||||||
chr5:136134081
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1119T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134081 | ||||||
chr5:136134255
|
G | A | 1 | a0001c0001t0002g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-245+1293G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134255 | ||||||
chr5:136134352
|
T | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1390T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134352 | ||||||
chr5:136134447
|
A | T | 1 | a0001c0001t0002g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-245+1485A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134447 | ||||||
chr5:136134493
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1531T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134493 | ||||||
chr5:136134576
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-245+1614A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134576 | ||||||
chr5:136134654
|
A | C | 2 | a0001c0001t0015g0021a0001c0001t0015g0079 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-245+1692A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134654 | ||||||
chr5:136134813
|
T | C | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-245+1851T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134813 | ||||||
chr5:136134855
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1893T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134855 | ||||||
chr5:136135086
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-245+2124G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135086 | ||||||
chr5:136135128
|
C | A | 1 | a0001c0001t0003g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-245+2166C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135128 | ||||||
chr5:136135345
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+2383T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135345 | ||||||
chr5:136135394
|
A | G | 1 | a0001c0001t0013g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-245+2432A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135394 | ||||||
chr5:136135411
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-245+2449G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135411 | ||||||
chr5:136135597
|
C | A | 1 | a0001c0001t0001g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-245+2635C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135597 | ||||||
chr5:136135823
|
C | T | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+2861C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135823 | ||||||
chr5:136135833
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-245+2871A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135833 | ||||||
chr5:136135950
|
C | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+2988C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135950 | ||||||
chr5:136135962
|
G | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3000G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135962 | ||||||
chr5:136136122
|
A | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3160A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136122 | ||||||
chr5:136136204
|
T | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3242T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136204 | ||||||
chr5:136136239
|
G | A | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+3277G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136239 | ||||||
chr5:136136285
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-245+3323C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136285 | ||||||
chr5:136136367
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-245+3405G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136367 | ||||||
chr5:136136384
|
G | T | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+3422G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136384 | ||||||
chr5:136136438
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-245+3476T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136438 | ||||||
chr5:136136505
|
G | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3543G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136505 | ||||||
chr5:136136563
|
A | C | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-245+3601A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136563 | ||||||
chr5:136136691
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-245+3729A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136691 | ||||||
chr5:136136726
|
T | C | 1 | a0001c0001t0021g0164 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-245+3764T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136726 | ||||||
chr5:136136735
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0077 | 3 | HG03041.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-245+3773C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136735 | ||||||
chr5:136136754
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0224 | 2 | HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-245+3792T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136754 | ||||||
chr5:136136759
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-245+3797C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136759 | ||||||
chr5:136136849
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-245+3887C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136849 | ||||||
chr5:136136898
|
C | T | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3936C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136898 | ||||||
chr5:136137016
|
G | A | 2 | a0001c0001t0015g0021a0001c0001t0015g0079 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-245+4054G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137016 | ||||||
chr5:136137017
|
A | AT | 14 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(11): Show | 14 | HG00621.hp1 HG00642.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-245+4075dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137017 | |||||
chr5:136137017
|
AT | A | 16 | a0001c0001t0001g0165a0001c0001t0002g0035a0001c0001t0002g0124others(13): Show | 17 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-245+4075delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137017 | |||||
chr5:136137017
|
ATT | A | 114 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(111): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-245+4074_-245+407 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137017 | |||||
chr5:136137040
|
C | G | 1 | a0001c0001t0001g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-245+4078C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137040 | ||||||
chr5:136137057
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-245+4095G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137057 | ||||||
chr5:136137059
|
T | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+4097T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137059 | ||||||
chr5:136137161
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-245+4199C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137161 | ||||||
chr5:136137188
|
A | G | 1 | a0001c0001t0023g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-245+4226A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137188 | ||||||
chr5:136137257
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+4295T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137257 | ||||||
chr5:136137258
|
G | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0084a0001c0001t0002g0085 | 4 | NA18953.hp2 NA19065.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-245+4296G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137258 | ||||||
chr5:136137270
|
A | ACCCC | 40 | a0001c0001t0002g0010a0001c0001t0002g0025a0001c0001t0002g0026others(37): Show | 48 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-245+4314_-245+431 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137270 | |||||
chr5:136137270
|
A | ACCCCC | 57 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(54): Show | 72 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-245+4313_-245+431 others(9): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137270 | |||||
chr5:136137270
|
A | ACCCCCC | 20 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0088others(17): Show | 22 | HG00597.hp2 HG01255.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-245+4312_-245+431 others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137270 | |||||
chr5:136137284
|
C | A | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+4322C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137284 | ||||||
chr5:136137292
|
A | G | 1 | a0001c0001t0004g0045 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-245+4330A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137292 | ||||||
chr5:136137306
|
C | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-245+4344C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137306 | ||||||
chr5:136137426
|
A | G | 2 | a0001c0001t0006g0116a0001c0001t0018g0013 | 3 | HG01516.hp1 HG01517.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-245+4464A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137426 | ||||||
chr5:136137491
|
C | T | 61 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(58): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-245+4529C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137491 | ||||||
chr5:136137799
|
A | C | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-245+4837A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137799 | ||||||
chr5:136137941
|
C | G | 3 | a0001c0001t0002g0026a0001c0001t0002g0093a0001c0001t0002g0115 | 4 | HG01099.hp1 HG01168.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-245+4979C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137941 | ||||||
chr5:136138003
|
A | G | 1 | a0001c0001t0008g0218 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-245+5041A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138003 | ||||||
chr5:136138073
|
G | A | 34 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0015others(31): Show | 44 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-245+5111G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138073 | ||||||
chr5:136138099
|
T | A | 3 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137 | 3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-245+5137T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138099 | ||||||
chr5:136138136
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+5174T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138136 | ||||||
chr5:136138406
|
C | T | 1 | a0001c0001t0001g0033 | 2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-245+5444C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138406 | ||||||
chr5:136138521
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+5559C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138521 | ||||||
chr5:136138615
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-245+5653A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138615 | ||||||
chr5:136138673
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-245+5711C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138673 | ||||||
chr5:136138757
|
A | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-245+5795A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138757 | ||||||
chr5:136138786
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-245+5824C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138786 | ||||||
chr5:136138811
|
A | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+5849A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138811 | ||||||
chr5:136138837
|
G | C | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+5875G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138837 | ||||||
chr5:136138980
|
G | A | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-245+6018G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138980 | ||||||
chr5:136139125
|
GCT | G | 10 | a0001c0001t0003g0018a0001c0001t0003g0036a0001c0001t0003g0056others(7): Show | 11 | HG01099.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-245+6166_-245+616 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139125 | |||||
chr5:136139126
|
C | CTG | 68 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(65): Show | 87 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.-245+6165_-245+616 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | |||||
chr5:136139126
|
C | CTGTG | 15 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0083others(12): Show | 16 | HG01928.hp1 HG01993.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.-245+6165_-245+616 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | |||||
chr5:136139126
|
C | CTGTGTG | 3 | a0001c0001t0013g0067a0001c0001t0017g0073a0001c0001t0017g0075 | 3 | HG02572.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-245+6165_-245+616 others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | |||||
chr5:136139126
|
CTCTG | C | 5 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0012g0037others(2): Show | 5 | HG00140.hp2 NA18979.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.-245+6166_-245+616 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | |||||
chr5:136139126
|
CTCTGTG | C | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-245+6166_-245+617 others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | |||||
chr5:136139128
|
C | CTG | 13 | a0001c0001t0001g0157a0001c0001t0001g0186a0001c0001t0001g0187others(10): Show | 13 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(10): Show |
intron_variant | MODIFIER | c.-245+6196_-245+619 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139128 | |||||
chr5:136139128
|
C | CTGTG | 3 | a0001c0001t0010g0158a0001c0001t0010g0159a0001c0001t0010g0190 | 3 | HG01243.hp1 HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-245+6194_-245+619 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139128 | |||||
chr5:136139128
|
C | G | 113 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(110): Show | 138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-245+6166C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139128 | ||||||
chr5:136139140
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0225 | 2 | NA18990.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-245+6178G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139140 | ||||||
chr5:136139234
|
T | C | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+6272T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139234 | ||||||
chr5:136139275
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-245+6313A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139275 | ||||||
chr5:136139280
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0232 | 2 | HG01952.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-245+6318A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139280 | ||||||
chr5:136139441
|
A | C | 1 | a0001c0001t0002g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-245+6479A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139441 | ||||||
chr5:136139450
|
G | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+6488G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139450 | ||||||
chr5:136139568
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-245+6606T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139568 | ||||||
chr5:136139590
|
C | T | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-245+6628C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139590 | ||||||
chr5:136139718
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0014g0071 | 2 | HG00597.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-245+6756C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139718 | ||||||
chr5:136139827
|
A | C | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-245+6865A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139827 | ||||||
chr5:136139827
|
A | G | 130 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(127): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.-245+6865A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139827 | ||||||
chr5:136139937
|
C | T | 5 | a0001c0001t0004g0006a0001c0001t0004g0042a0001c0001t0004g0043others(2): Show | 6 | HG01258.hp2 HG01346.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-245+6975C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139937 | ||||||
chr5:136140023
|
C | CT | 7 | a0001c0001t0001g0156a0001c0001t0002g0095a0001c0001t0007g0001others(4): Show | 11 | HG02615.hp2 HG02809.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-245+7078dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136140023 | |||||
chr5:136140023
|
CT | C | 6 | a0001c0001t0001g0226a0001c0001t0002g0117a0001c0001t0013g0078others(3): Show | 6 | HG01496.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-245+7078delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136140023 | |||||
chr5:136140228
|
C | T | 2 | a0001c0001t0002g0009a0001c0001t0002g0127 | 4 | NA18941.hp2 NA18945.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-245+7266C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136140228 | ||||||
chr5:136141075
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-6757T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141075 | ||||||
chr5:136141088
|
T | C | 119 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(116): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-244-6744T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141088 | ||||||
chr5:136141173
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-244-6659A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141173 | ||||||
chr5:136141179
|
T | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02083.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-244-6653T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141179 | ||||||
chr5:136141197
|
A | T | 1 | a0001c0001t0002g0114 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-244-6635A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141197 | ||||||
chr5:136141254
|
C | A | 1 | a0001c0001t0002g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-244-6578C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141254 | ||||||
chr5:136141494
|
C | T | 2 | a0001c0001t0003g0054a0001c0001t0003g0063 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-244-6338C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141494 | ||||||
chr5:136141604
|
C | T | 1 | a0001c0001t0018g0013 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-244-6228C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141604 | ||||||
chr5:136141702
|
TAAAG | T | 3 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137 | 3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-244-6127_-244-612 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136141702 | |||||
chr5:136141836
|
C | A | 1 | a0001c0001t0004g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-244-5996C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141836 | ||||||
chr5:136141936
|
G | C | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5896G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141936 | ||||||
chr5:136141937
|
C | A | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5895C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141937 | ||||||
chr5:136141938
|
A | G | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5894A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141938 | ||||||
chr5:136141940
|
T | C | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5892T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141940 | ||||||
chr5:136141941
|
TTA | T | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5890_-244-588 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141941 | ||||||
chr5:136141944
|
A | G | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5888A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141944 | ||||||
chr5:136142032
|
C | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-244-5800C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142032 | ||||||
chr5:136142276
|
G | A | 3 | a0001c0001t0013g0067a0001c0001t0013g0072a0001c0001t0014g0071 | 3 | HG02486.hp1 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-244-5556G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142276 | ||||||
chr5:136142621
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-244-5211C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142621 | ||||||
chr5:136142843
|
C | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0057 | 2 | HG01099.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-244-4989C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142843 | ||||||
chr5:136142966
|
G | T | 1 | a0001c0001t0003g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-244-4866G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142966 | ||||||
chr5:136142972
|
C | T | 1 | a0001c0001t0003g0017 | 2 | NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-244-4860C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142972 | ||||||
chr5:136143035
|
A | C | 2 | a0001c0001t0010g0159a0001c0001t0010g0190 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.-244-4797A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143035 | ||||||
chr5:136143113
|
A | G | 1 | a0001c0001t0013g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-244-4719A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143113 | ||||||
chr5:136143198
|
A | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244-4634A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143198 | ||||||
chr5:136143266
|
C | CT | 67 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(64): Show | 83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-244-4552dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136143266 | |||||
chr5:136143659
|
A | C | 119 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(116): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-244-4173A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143659 | ||||||
chr5:136143734
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-244-4098T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143734 | ||||||
chr5:136143746
|
C | G | 1 | a0001c0001t0002g0109 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-244-4086C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143746 | ||||||
chr5:136144055
|
A | G | 2 | a0001c0001t0004g0006a0001c0001t0025g0006 | 3 | HG02451.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-244-3777A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144055 | ||||||
chr5:136144085
|
C | T | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-3747C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144085 | ||||||
chr5:136144325
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0166 | 2 | HG00408.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-244-3507G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144325 | ||||||
chr5:136144392
|
AGCAAAAA others(18): Show |
A | 3 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137 | 3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-244-3439_-244-341 others(29): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144392 | ||||||
chr5:136144429
|
G | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-3403G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144429 | ||||||
chr5:136144721
|
A | G | 1 | a0001c0001t0006g0120 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-244-3111A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144721 | ||||||
chr5:136144753
|
T | G | 4 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0114others(1): Show | 5 | HG02559.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244-3079T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144753 | ||||||
chr5:136145065
|
G | A | 1 | a0001c0001t0004g0044 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-244-2767G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145065 | ||||||
chr5:136145116
|
A | AT | 130 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(127): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.-244-2706dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136145116 | |||||
chr5:136145370
|
C | A | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-2462C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145370 | ||||||
chr5:136145539
|
TC | T | 8 | a0001c0001t0004g0006a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244-2292delC | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145539 | ||||||
chr5:136145672
|
T | C | 61 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(58): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-244-2160T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145672 | ||||||
chr5:136145983
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0167 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-244-1849T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145983 | ||||||
chr5:136146001
|
A | G | 4 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0114others(1): Show | 5 | HG02559.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244-1831A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146001 | ||||||
chr5:136146018
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-244-1814G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146018 | ||||||
chr5:136146457
|
G | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-1375G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146457 | ||||||
chr5:136146508
|
T | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-1324T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146508 | ||||||
chr5:136146527
|
T | G | 1 | a0001c0001t0013g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-244-1305T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146527 | ||||||
chr5:136146580
|
G | T | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-244-1252G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146580 | ||||||
chr5:136146681
|
G | C | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-244-1151G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146681 | ||||||
chr5:136146846
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-244-986G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146846 | ||||||
chr5:136146896
|
C | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-936C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146896 | ||||||
chr5:136147138
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-244-694G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147138 | ||||||
chr5:136147324
|
G | A | 42 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0015others(39): Show | 53 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-244-508G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147324 | ||||||
chr5:136147332
|
G | T | 125 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(122): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-244-500G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147332 | ||||||
chr5:136147645
|
A | G | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-244-187A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147645 | ||||||
chr5:136147691
|
A | G | 1 | a0001c0001t0018g0013 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-244-141A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147691 | ||||||
chr5:136147819
|
A | AT | 111 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(108): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
splice_acceptor_variant&intron_variant | HIGH | c.-244-3dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136147819 | |||||
chr5:136147819
|
A | T | 9 | a0001c0001t0003g0077a0001c0001t0004g0006a0001c0001t0004g0040others(6): Show | 10 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-244-13A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147819 | ||||||
chr5:136148163
|
T | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-170+257T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148163 | ||||||
chr5:136148200
|
A | G | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-170+294A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148200 | ||||||
chr5:136148254
|
G | GT | 126 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(123): Show | 156 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-170+350dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 136148254 | |||||
chr5:136148257
|
C | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+351C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148257 | ||||||
chr5:136148323
|
T | A | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-170+417T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148323 | ||||||
chr5:136148324
|
G | T | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-170+418G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148324 | ||||||
chr5:136148363
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-170+457T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148363 | ||||||
chr5:136148459
|
T | A | 7 | a0001c0001t0001g0034a0001c0001t0001g0168a0001c0001t0001g0198others(4): Show | 8 | HG00099.hp1 HG00642.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-170+553T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148459 | ||||||
chr5:136148500
|
C | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+594C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148500 | ||||||
chr5:136148830
|
C | T | 1 | a0001c0001t0014g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-170+924C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148830 | ||||||
chr5:136148832
|
C | T | 1 | a0001c0001t0022g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-170+926C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148832 | ||||||
chr5:136148874
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+968A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148874 | ||||||
chr5:136148909
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-170+1003A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148909 | ||||||
chr5:136149139
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-170+1233A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149139 | ||||||
chr5:136149247
|
G | C | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-170+1341G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149247 | ||||||
chr5:136149288
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137 | 3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-170+1382T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149288 | ||||||
chr5:136149298
|
T | C | 2 | a0001c0001t0013g0067a0001c0001t0014g0071 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-170+1392T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149298 | ||||||
chr5:136149332
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-170+1426T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149332 | ||||||
chr5:136149337
|
C | T | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-170+1431C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149337 | ||||||
chr5:136149433
|
A | G | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-170+1527A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149433 | ||||||
chr5:136149440
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+1534A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149440 | ||||||
chr5:136149482
|
C | CT | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-170+1590dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 136149482 | |||||
chr5:136149708
|
C | T | 63 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(60): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-170+1802C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149708 | ||||||
chr5:136149742
|
C | A | 119 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(116): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-170+1836C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149742 | ||||||
chr5:136149804
|
A | C | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-170+1898A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149804 | ||||||
chr5:136149805
|
G | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-170+1899G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149805 | ||||||
chr5:136149926
|
A | G | 120 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(117): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.-170+2020A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149926 | ||||||
chr5:136149984
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-170+2078A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149984 | ||||||
chr5:136150341
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-170+2435G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150341 | ||||||
chr5:136150441
|
C | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+2535C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150441 | ||||||
chr5:136150519
|
T | C | 49 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(46): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-170+2613T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150519 | ||||||
chr5:136150631
|
A | G | 2 | a0001c0001t0004g0006a0001c0001t0025g0006 | 3 | HG02451.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-170+2725A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150631 | ||||||
chr5:136150678
|
A | T | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-170+2772A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150678 | ||||||
chr5:136150695
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0003g0047 | 2 | HG02738.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-170+2789G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150695 | ||||||
chr5:136150696
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-170+2790T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150696 | ||||||
chr5:136150847
|
G | T | 127 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(124): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-169-2745G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150847 | ||||||
chr5:136150887
|
T | G | 5 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG01928.hp2 HG01952.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-169-2705T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150887 | ||||||
chr5:136151050
|
A | G | 9 | a0001c0001t0002g0035a0001c0001t0002g0096a0001c0001t0002g0099others(6): Show | 9 | HG00140.hp1 HG00673.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-169-2542A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151050 | ||||||
chr5:136151153
|
A | G | 5 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG01928.hp2 HG01952.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-169-2439A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151153 | ||||||
chr5:136151175
|
TG | T | 9 | a0001c0001t0003g0077a0001c0001t0004g0006a0001c0001t0004g0040others(6): Show | 10 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-169-2415delG | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 136151175 | |||||
chr5:136151626
|
G | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1966G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151626 | ||||||
chr5:136151691
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-169-1901C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151691 | ||||||
chr5:136151719
|
A | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-169-1873A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151719 | ||||||
chr5:136151737
|
A | T | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-1855A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151737 | ||||||
chr5:136151780
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1812A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151780 | ||||||
chr5:136151804
|
A | T | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-1788A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151804 | ||||||
chr5:136151820
|
G | C | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1772G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151820 | ||||||
chr5:136151854
|
A | G | 1 | a0001c0001t0003g0052 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-169-1738A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151854 | ||||||
chr5:136151952
|
G | T | 1 | a0001c0001t0003g0051 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-169-1640G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151952 | ||||||
chr5:136152263
|
G | T | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-169-1329G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152263 | ||||||
chr5:136152464
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1128A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152464 | ||||||
chr5:136152611
|
G | T | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-981G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152611 | ||||||
chr5:136152707
|
C | T | 8 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(5): Show | 10 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-169-885C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152707 | ||||||
chr5:136152797
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0233a0001c0001t0013g0078 | 3 | HG03130.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-169-795G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152797 | ||||||
chr5:136152876
|
T | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0156others(2): Show | 10 | NA18941.hp1 NA18964.hp1 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.-169-716T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152876 | ||||||
chr5:136153041
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-169-551G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136153041 | ||||||
chr5:136153215
|
G | A | 1 | a0001c0001t0018g0013 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-169-377G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136153215 | ||||||
chr5:136153536
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-56A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136153536 | ||||||
chr5:136154202
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.403+39A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154202 | ||||||
chr5:136154384
|
G | A | 1 | a0001c0001t0029g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403+221G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154384 | ||||||
chr5:136154493
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.403+330A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154493 | ||||||
chr5:136154948
|
G | A | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.403+785G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154948 | ||||||
chr5:136154954
|
CTT | C | 3 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137 | 3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.403+793_403+794del others(2): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136154954 | |||||
chr5:136154964
|
G | A | 7 | a0001c0001t0001g0163a0001c0001t0004g0006a0001c0001t0004g0041others(4): Show | 8 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+801G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154964 | ||||||
chr5:136155046
|
A | G | 1 | a0001c0001t0015g0079 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.403+883A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155046 | ||||||
chr5:136155127
|
C | T | 1 | a0001c0001t0027g0122 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.403+964C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155127 | ||||||
chr5:136155128
|
A | G | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.403+965A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155128 | ||||||
chr5:136155196
|
G | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0057 | 2 | HG01099.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.403+1033G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155196 | ||||||
chr5:136155222
|
A | G | 1 | a0001c0001t0018g0013 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.403+1059A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155222 | ||||||
chr5:136155293
|
T | C | 1 | a0001c0001t0012g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.403+1130T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155293 | ||||||
chr5:136155457
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.403+1294G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155457 | ||||||
chr5:136155707
|
C | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.403+1544C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155707 | ||||||
chr5:136155887
|
T | G | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+1724T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155887 | ||||||
chr5:136156276
|
G | C | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.403+2113G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156276 | ||||||
chr5:136156355
|
T | A | 1 | a0001c0001t0002g0089 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.403+2192T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156355 | ||||||
chr5:136156708
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.403+2545C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156708 | ||||||
chr5:136156824
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.403+2661C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156824 | ||||||
chr5:136156835
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0221 | 2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.403+2672C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156835 | ||||||
chr5:136156955
|
A | AC | 44 | a0001c0001t0002g0023a0001c0001t0003g0003a0001c0001t0003g0014others(41): Show | 56 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.403+2798dupC | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136156955 | |||||
chr5:136156980
|
C | T | 1 | a0001c0001t0018g0013 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.403+2817C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156980 | ||||||
chr5:136157201
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(241): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.403+3038T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157201 | ||||||
chr5:136157512
|
A | T | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.404-3344A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157512 | ||||||
chr5:136157615
|
G | A | 2 | a0001c0001t0015g0021a0001c0001t0015g0079 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.404-3241G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157615 | ||||||
chr5:136157712
|
G | A | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.404-3144G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157712 | ||||||
chr5:136157759
|
C | T | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-3097C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157759 | ||||||
chr5:136157879
|
G | A | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-2977G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157879 | ||||||
chr5:136157899
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.404-2957G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157899 | ||||||
chr5:136157900
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.404-2956G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157900 | ||||||
chr5:136158171
|
C | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.404-2685C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158171 | ||||||
chr5:136158223
|
G | A | 1 | a0001c0002t0001g0029 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.404-2633G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158223 | ||||||
chr5:136158283
|
A | T | 1 | a0001c0001t0002g0092 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.404-2573A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158283 | ||||||
chr5:136158332
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-2524A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158332 | ||||||
chr5:136158385
|
T | C | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.404-2471T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158385 | ||||||
chr5:136158472
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0221 | 2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.404-2384C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158472 | ||||||
chr5:136158538
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.404-2318A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158538 | ||||||
chr5:136158548
|
A | C | 1 | a0001c0001t0013g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-2308A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158548 | ||||||
chr5:136158563
|
G | C | 1 | a0001c0001t0005g0131 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-2293G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158563 | ||||||
chr5:136158656
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.404-2200T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158656 | ||||||
chr5:136158696
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.404-2160G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158696 | ||||||
chr5:136158823
|
C | G | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-2033C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158823 | ||||||
chr5:136158823
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.404-2033C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158823 | ||||||
chr5:136158878
|
G | A | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.404-1978G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158878 | ||||||
chr5:136158898
|
C | CA | 128 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(125): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.404-1947dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136158898 | |||||
chr5:136158987
|
G | A | 2 | a0001c0001t0015g0021a0001c0001t0015g0079 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.404-1869G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158987 | ||||||
chr5:136159001
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.404-1855T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159001 | ||||||
chr5:136159049
|
T | A | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-1807T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159049 | ||||||
chr5:136159167
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.404-1689T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159167 | ||||||
chr5:136159179
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0099 | 2 | HG00673.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.404-1677G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159179 | ||||||
chr5:136159336
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0165 | 3 | NA18956.hp2 NA19001.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.404-1520T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159336 | ||||||
chr5:136159489
|
C | T | 1 | a0001c0001t0003g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.404-1367C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159489 | ||||||
chr5:136159505
|
A | G | 1 | a0001c0001t0013g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-1351A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159505 | ||||||
chr5:136159589
|
T | A | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-1267T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159589 | ||||||
chr5:136159634
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.404-1222A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159634 | ||||||
chr5:136159645
|
C | CT | 114 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(111): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.404-1210dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136159645 | |||||
chr5:136159768
|
G | A | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.404-1088G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159768 | ||||||
chr5:136160011
|
T | G | 1 | a0001c0001t0004g0045 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.404-845T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160011 | ||||||
chr5:136160083
|
C | T | 1 | a0001c0001t0002g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.404-773C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160083 | ||||||
chr5:136160312
|
T | A | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-544T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160312 | ||||||
chr5:136160755
|
G | A | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-101G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160755 | ||||||
chr5:136161131
|
C | CA | 124 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(121): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.655+37dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136161131 | |||||
chr5:136161131
|
C | CAA | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+36_655+37dupAA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136161131 | |||||
chr5:136161145
|
T | A | 1 | a0001c0001t0031g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.655+38T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161145 | ||||||
chr5:136161153
|
A | C | 1 | a0001c0001t0013g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.655+46A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161153 | ||||||
chr5:136161206
|
TATA | T | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.655+103_655+105del others(3): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136161206 | |||||
chr5:136161540
|
G | C | 2 | a0001c0001t0004g0006a0001c0001t0025g0006 | 3 | HG02451.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.655+433G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161540 | ||||||
chr5:136161582
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.655+475G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161582 | ||||||
chr5:136162094
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.655+987C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162094 | ||||||
chr5:136162124
|
A | G | 8 | a0001c0001t0002g0008a0001c0001t0002g0025a0001c0001t0002g0086others(5): Show | 11 | HG00597.hp2 HG00621.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.655+1017A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162124 | ||||||
chr5:136162320
|
G | A | 8 | a0001c0001t0004g0006a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-952G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162320 | ||||||
chr5:136162487
|
T | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-785T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162487 | ||||||
chr5:136162553
|
A | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.656-719A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162553 | ||||||
chr5:136162630
|
C | G | 1 | a0001c0001t0005g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.656-642C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162630 | ||||||
chr5:136162732
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-540C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162732 | ||||||
chr5:136162840
|
G | A | 5 | a0001c0001t0004g0006a0001c0001t0004g0042a0001c0001t0004g0043others(2): Show | 6 | HG01258.hp2 HG01346.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-432G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162840 | ||||||
chr5:136162851
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.656-421C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162851 | ||||||
chr5:136162861
|
T | G | 1 | a0001c0001t0031g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.656-411T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162861 | ||||||
chr5:136163011
|
A | C | 1 | a0001c0001t0002g0088 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.656-261A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136163011 | ||||||
chr5:136163092
|
A | G | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.656-180A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136163092 | ||||||
chr5:136163156
|
T | C | 4 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137others(1): Show | 5 | HG01496.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-116T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136163156 | ||||||
chr5:136163255
|
AT | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.656-9delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136163255 | |||||
chr5:136163522
|
T | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+131T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163522 | ||||||
chr5:136163607
|
G | A | 2 | a0001c0001t0003g0054a0001c0001t0003g0063 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.775+216G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163607 | ||||||
chr5:136163711
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.775+320A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163711 | ||||||
chr5:136163884
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.775+493A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163884 | ||||||
chr5:136163960
|
C | A | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.775+569C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163960 | ||||||
chr5:136164132
|
G | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+741G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164132 | ||||||
chr5:136164183
|
G | A | 4 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137others(1): Show | 5 | HG01496.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+792G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164183 | ||||||
chr5:136164232
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.775+841T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164232 | ||||||
chr5:136164314
|
C | T | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.775+923C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164314 | ||||||
chr5:136164533
|
T | A | 7 | a0001c0001t0002g0035a0001c0001t0002g0096a0001c0001t0002g0099others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+1142T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164533 | ||||||
chr5:136164569
|
G | A | 1 | a0001c0001t0004g0045 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.775+1178G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164569 | ||||||
chr5:136164707
|
G | A | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.775+1316G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164707 | ||||||
chr5:136164743
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.775+1352T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164743 | ||||||
chr5:136164858
|
T | G | 5 | a0001c0001t0001g0150a0001c0001t0001g0160a0001c0001t0001g0175others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+1467T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164858 | ||||||
chr5:136165373
|
T | G | 3 | a0001c0001t0002g0113a0001c0001t0015g0021a0001c0001t0015g0079 | 4 | HG01167.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+1982T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165373 | ||||||
chr5:136165377
|
G | T | 8 | a0001c0001t0002g0027a0001c0001t0002g0091a0001c0001t0002g0096others(5): Show | 9 | HG00673.hp1 HG02040.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.775+1986G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165377 | ||||||
chr5:136165393
|
T | G | 63 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(60): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.775+2002T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165393 | ||||||
chr5:136165421
|
T | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+2030T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165421 | ||||||
chr5:136165639
|
C | T | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+2248C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165639 | ||||||
chr5:136165662
|
A | AT | 6 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0155others(3): Show | 6 | HG02056.hp2 HG02071.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+2308dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165662
|
AT | A | 34 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0140others(31): Show | 35 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.775+2308delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165662
|
ATTTTTTT others(2): Show |
A | 5 | a0001c0001t0002g0087a0001c0001t0007g0001a0001c0001t0007g0070others(2): Show | 9 | HG00423.hp2 HG02056.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+2300_775+2308d others(11): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165662
|
ATTTTTTT others(3): Show |
A | 58 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(55): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.775+2299_775+2308d others(12): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165662
|
ATTTTTTT others(4): Show |
A | 50 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0091others(47): Show | 61 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.775+2298_775+2308d others(13): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165662
|
ATTTTTTT others(5): Show |
A | 9 | a0001c0001t0003g0059a0001c0001t0003g0138a0001c0001t0005g0028others(6): Show | 11 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.775+2297_775+2308d others(14): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165662
|
ATTTTTTT others(6): Show |
A | 7 | a0001c0001t0001g0169a0001c0001t0008g0196a0001c0001t0013g0078others(4): Show | 8 | HG01167.hp2 HG01496.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.775+2296_775+2308d others(15): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165662
|
ATTTTTTT others(8): Show |
A | 5 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039others(2): Show | 5 | HG02895.hp2 HG02897.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+2294_775+2308d others(17): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | |||||
chr5:136165663
|
T | TA | 9 | a0001c0001t0001g0192a0001c0001t0001g0198a0001c0001t0001g0199others(6): Show | 9 | HG01175.hp1 HG01952.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+2272_775+2273i others(3): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165663 | ||||||
chr5:136165664
|
T | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0033others(23): Show | 36 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.775+2273T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165664 | ||||||
chr5:136165665
|
T | A | 12 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0178others(9): Show | 12 | HG01069.hp1 HG01884.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.775+2274T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165665 | ||||||
chr5:136165666
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.775+2275T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165666 | ||||||
chr5:136165670
|
T | A | 1 | a0001c0001t0010g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.775+2279T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165670 | ||||||
chr5:136165672
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.775+2281T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165672 | ||||||
chr5:136165673
|
T | A | 5 | a0001c0001t0002g0087a0001c0001t0007g0001a0001c0001t0007g0070others(2): Show | 9 | HG00423.hp2 HG02056.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+2282T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165673 | ||||||
chr5:136165674
|
T | A | 58 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(55): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.775+2283T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165674 | ||||||
chr5:136165675
|
T | A | 50 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0091others(47): Show | 61 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.775+2284T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165675 | ||||||
chr5:136165676
|
T | A | 9 | a0001c0001t0003g0059a0001c0001t0003g0138a0001c0001t0005g0028others(6): Show | 11 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.775+2285T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165676 | ||||||
chr5:136165677
|
T | A | 6 | a0001c0001t0001g0169a0001c0001t0013g0078a0001c0001t0014g0136others(3): Show | 7 | HG01167.hp2 HG01496.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+2286T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165677 | ||||||
chr5:136165679
|
T | A | 5 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039others(2): Show | 5 | HG02895.hp2 HG02897.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+2288T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165679 | ||||||
chr5:136165890
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.775+2499G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165890 | ||||||
chr5:136165933
|
A | G | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.775+2542A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165933 | ||||||
chr5:136166035
|
T | C | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+2644T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166035 | ||||||
chr5:136166054
|
A | T | 1 | a0001c0001t0005g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.775+2663A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166054 | ||||||
chr5:136166155
|
A | AT | 23 | a0001c0001t0003g0003a0001c0001t0003g0014a0001c0001t0003g0015others(20): Show | 31 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.775+2772dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136166155 | |||||
chr5:136166166
|
C | CT | 12 | a0001c0001t0001g0238a0001c0001t0003g0014a0001c0001t0003g0015others(9): Show | 14 | HG01993.hp1 HG02602.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.775+2788dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136166166 | |||||
chr5:136166240
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.775+2849T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166240 | ||||||
chr5:136166305
|
C | T | 1 | a0001c0001t0021g0164 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.775+2914C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166305 | ||||||
chr5:136166437
|
A | G | 130 | a0001c0001t0001g0210a0001c0001t0002g0007a0001c0001t0002g0008others(127): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.775+3046A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166437 | ||||||
chr5:136166510
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.775+3119A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166510 | ||||||
chr5:136166571
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.775+3180A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166571 | ||||||
chr5:136166712
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+3321A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166712 | ||||||
chr5:136166728
|
C | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+3337C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166728 | ||||||
chr5:136166786
|
T | C | 2 | a0001c0001t0015g0021a0001c0001t0015g0079 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.775+3395T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166786 | ||||||
chr5:136166820
|
C | T | 2 | a0001c0001t0009g0153a0001c0003t0009g0154 | 2 | HG00323.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.775+3429C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166820 | ||||||
chr5:136166895
|
A | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.775+3504A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166895 | ||||||
chr5:136166904
|
C | T | 6 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0187others(3): Show | 6 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+3513C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166904 | ||||||
chr5:136167084
|
A | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+3693A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167084 | ||||||
chr5:136167170
|
AT | A | 130 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(127): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.775+3790delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136167170 | |||||
chr5:136167181
|
T | C | 1 | a0001c0001t0031g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.775+3790T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167181 | ||||||
chr5:136167265
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.775+3874G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167265 | ||||||
chr5:136167289
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0142 | 2 | NA18952.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.775+3898C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167289 | ||||||
chr5:136167412
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.775+4021C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167412 | ||||||
chr5:136167460
|
T | A | 1 | a0001c0001t0003g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.775+4069T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167460 | ||||||
chr5:136167670
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0084a0001c0001t0002g0085 | 4 | NA18953.hp2 NA19065.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+4279C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167670 | ||||||
chr5:136167810
|
T | G | 1 | a0001c0001t0003g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.775+4419T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167810 | ||||||
chr5:136167891
|
G | A | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.775+4500G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167891 | ||||||
chr5:136168296
|
A | G | 1 | a0001c0001t0006g0103 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.776-4138A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136168296 | ||||||
chr5:136168393
|
GTTGTT | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.776-4033_776-4029d others(7): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136168393 | |||||
chr5:136168490
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.776-3944C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136168490 | ||||||
chr5:136169001
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.776-3433T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169001 | ||||||
chr5:136169008
|
G | A | 1 | a0001c0001t0014g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.776-3426G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169008 | ||||||
chr5:136169291
|
C | T | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(128): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.776-3143C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169291 | ||||||
chr5:136169299
|
C | T | 1 | a0001c0001t0002g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.776-3135C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169299 | ||||||
chr5:136169387
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.776-3047C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169387 | ||||||
chr5:136169506
|
AGTTT | A | 3 | a0001c0001t0007g0001a0001c0001t0007g0070a0001c0001t0030g0001 | 7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.776-2923_776-2920d others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136169506 | |||||
chr5:136169829
|
T | C | 1 | a0001c0001t0029g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.776-2605T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169829 | ||||||
chr5:136169938
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-2496A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169938 | ||||||
chr5:136170152
|
G | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-2282G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170152 | ||||||
chr5:136170264
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-2170A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170264 | ||||||
chr5:136170428
|
G | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-2006G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170428 | ||||||
chr5:136170606
|
A | G | 4 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137others(1): Show | 5 | HG01496.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.776-1828A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170606 | ||||||
chr5:136170618
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137 | 3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.776-1816T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170618 | ||||||
chr5:136170708
|
T | C | 1 | a0001c0001t0014g0071 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.776-1726T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170708 | ||||||
chr5:136170774
|
T | C | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-1660T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170774 | ||||||
chr5:136170788
|
A | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0040a0001c0001t0004g0041others(5): Show | 9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.776-1646A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170788 | ||||||
chr5:136170951
|
C | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-1483C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170951 | ||||||
chr5:136170985
|
A | G | 1 | a0001c0001t0020g0123 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.776-1449A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170985 | ||||||
chr5:136171008
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.776-1426A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171008 | ||||||
chr5:136171017
|
C | T | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-1417C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171017 | ||||||
chr5:136171106
|
G | T | 1 | a0001c0001t0003g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.776-1328G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171106 | ||||||
chr5:136171157
|
A | G | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.776-1277A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171157 | ||||||
chr5:136171164
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-1270A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171164 | ||||||
chr5:136171263
|
T | G | 2 | a0001c0001t0013g0067a0001c0001t0014g0071 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.776-1171T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171263 | ||||||
chr5:136171374
|
A | G | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.776-1060A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171374 | ||||||
chr5:136171457
|
C | G | 1 | a0001c0001t0002g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.776-977C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171457 | ||||||
chr5:136171565
|
C | T | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-869C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171565 | ||||||
chr5:136171590
|
T | A | 1 | a0001c0001t0001g0011 | 3 | NA18964.hp1 NA18988.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.776-844T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171590 | ||||||
chr5:136171720
|
T | C | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.776-714T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171720 | ||||||
chr5:136171878
|
A | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-556A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171878 | ||||||
chr5:136171935
|
T | C | 1 | a0001c0001t0018g0013 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.776-499T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171935 | ||||||
chr5:136172133
|
C | G | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-301C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172133 | ||||||
chr5:136172190
|
C | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-244C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172190 | ||||||
chr5:136172217
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.776-217C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172217 | ||||||
chr5:136172243
|
G | A | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.776-191G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172243 | ||||||
chr5:136172425
|
T | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0059 | 3 | NA18961.hp2 NA18965.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.776-9T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172425 | ||||||
chr5:136172692
|
A | G | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.997+37A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136172692 | ||||||
chr5:136172722
|
A | G | 8 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(5): Show | 10 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.997+67A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136172722 | ||||||
chr5:136172797
|
G | A | 1 | a0001c0001t0013g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.997+142G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136172797 | ||||||
chr5:136173225
|
C | CA | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.997+571dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 136173225 | |||||
chr5:136173286
|
G | T | 1 | a0001c0001t0002g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.997+631G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173286 | ||||||
chr5:136173418
|
A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0145 | 3 | NA18947.hp1 NA19056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.997+763A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173418 | ||||||
chr5:136173541
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.998-835T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173541 | ||||||
chr5:136173597
|
T | A | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.998-779T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173597 | ||||||
chr5:136173654
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.998-722T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173654 | ||||||
chr5:136173756
|
T | C | 3 | a0001c0001t0013g0078a0001c0001t0014g0136a0001c0001t0014g0137 | 3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.998-620T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173756 | ||||||
chr5:136173912
|
C | G | 2 | a0001c0001t0017g0073a0001c0001t0017g0075 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.998-464C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173912 | ||||||
chr5:136173941
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0156others(2): Show | 10 | NA18941.hp1 NA18964.hp1 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.998-435T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173941 | ||||||
chr5:136173943
|
G | GT | 7 | a0001c0001t0003g0047a0001c0001t0005g0028a0001c0001t0005g0131others(4): Show | 8 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.998-424dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 136173943 | |||||
chr5:136174032
|
G | C | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.998-344G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174032 | ||||||
chr5:136174163
|
C | A | 128 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(125): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.998-213C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174163 | ||||||
chr5:136174163
|
C | G | 1 | a0001c0001t0005g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.998-213C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174163 | ||||||
chr5:136174183
|
C | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.998-193C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174183 | ||||||
chr5:136174328
|
A | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0221 | 2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.998-48A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174328 | ||||||
chr5:136174344
|
T | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.998-32T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174344 | ||||||
chr5:136174349
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.998-27G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174349 | ||||||
chr5:136174365
|
G | A | 6 | a0001c0001t0005g0028a0001c0001t0005g0131a0001c0001t0005g0132others(3): Show | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-11G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174365 | ||||||
chr5:136174741
|
C | G | 62 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(59): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1254+109C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136174741 | ||||||
chr5:136175057
|
CAA | C | 62 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(59): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1254+427_1254+428d others(4): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136175057 | |||||
chr5:136175470
|
T | A | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1254+838T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175470 | ||||||
chr5:136175517
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1254+885A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175517 | ||||||
chr5:136175521
|
A | G | 1 | a0001c0001t0003g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1254+889A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175521 | ||||||
chr5:136175687
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1254+1055C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175687 | ||||||
chr5:136175852
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0206 | 2 | HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1254+1220C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175852 | ||||||
chr5:136175878
|
G | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1254+1246G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175878 | ||||||
chr5:136175988
|
A | G | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1255-1349A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175988 | ||||||
chr5:136176176
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG00621.hp1 NA18970.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1255-1161G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176176 | ||||||
chr5:136176387
|
G | A | 2 | a0001c0001t0016g0080a0001c0001t0016g0081 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1255-950G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176387 | ||||||
chr5:136176406
|
G | A | 3 | a0001c0001t0012g0037a0001c0001t0012g0038a0001c0001t0012g0039 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1255-931G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176406 | ||||||
chr5:136176457
|
C | CA | 17 | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0001t0001g0175others(14): Show | 17 | HG00423.hp1 HG00621.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1255-854dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
C | CAAA | 2 | a0001c0001t0007g0001a0001c0001t0030g0001 | 6 | HG02615.hp2 HG02976.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-856_1255-854d others(5): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
C | CAAAAAAA others(1): Show |
4 | a0001c0001t0005g0028a0001c0001t0005g0134a0001c0001t0005g0135others(1): Show | 6 | HG01069.hp2 HG01884.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-861_1255-854d others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0012g0037 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1255-868_1255-854d others(17): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0012g0038 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1255-876_1255-854d others(25): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0012g0039 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1255-878_1255-854d others(27): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
CAAAA | C | 10 | a0001c0001t0002g0126a0001c0001t0003g0058a0001c0001t0003g0064others(7): Show | 11 | HG01496.hp2 HG02257.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255-857_1255-854d others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
CAAAAA | C | 95 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(92): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1255-858_1255-854d others(7): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
CAAAAAA | C | 6 | a0001c0001t0002g0085a0001c0001t0002g0091a0001c0001t0003g0047others(3): Show | 6 | HG02602.hp1 HG02735.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-859_1255-854d others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176457
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0013g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1255-866_1255-854d others(15): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | |||||
chr5:136176833
|
G | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG00621.hp1 NA18970.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1255-504G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176833 | ||||||
chr5:136176983
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0002g0112 | 2 | HG01928.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1255-354A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176983 | ||||||
chr5:136177077
|
A | T | 1 | a0001c0001t0029g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1255-260A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136177077 | ||||||
chr5:136177227
|
C | A | 129 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(126): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1255-110C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136177227 | ||||||
chr5:136177248
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1255-89A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136177248 |