geneid | 89122 |
---|---|
ensemblid | ENSG00000146833.16 |
hgncid | 16275 |
symbol | TRIM4 |
name | tripartite motif containing 4 |
refseq_nuc | NM_033091.3 |
refseq_prot | NP_149082.1 |
ensembl_nuc | ENST00000349062.7 |
ensembl_prot | ENSP00000275736.4 |
mane_status | MANE Select |
chr | chr7 |
start | 99890403 |
end | 99919530 |
strand | - |
ver | v1.2 |
region | chr7:99890403-99919530 |
region5000 | chr7:99885403-99924530 |
regionname0 | TRIM4_chr7_99890403_99919530 |
regionname5000 | TRIM4_chr7_99885403_99924530 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 474 | 283 | 62 | 57 | 112 | 13 | 37 | 84 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0002 | 0/0 | 474 | 16 | 0 | 1 | 15 | 0 | 0 | 14 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0003 | 0/0 | 474 | 13 | 7 | 2 | 0 | 1 | 3 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0004 | 0/0 | 474 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0005 | 0/0 | 474 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0006 | 0/0 | 474 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0007 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1425 | 121 | 5 | 28 | 65 | 5 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0002 | 0/0 | 1425 | 101 | 11 | 23 | 45 | 6 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0003 | 0/0 | 1425 | 56 | 45 | 6 | 0 | 2 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0004 | 0/0 | 1425 | 16 | 0 | 1 | 15 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0005 | 0/0 | 1425 | 13 | 7 | 2 | 0 | 1 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0006 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0007 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0008 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0009 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0010 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0011 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0012 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
c0013 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1890 | 182 | 60 | 30 | 61 | 8 | 23 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0002 | 1/1 | 1890 | 112 | 4 | 24 | 61 | 5 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0003 | 0/0 | 1890 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0004 | 0/0 | 1890 | 5 | 0 | 4 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0005 | 0/0 | 1890 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0006 | 0/0 | 1890 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0007 | 0/0 | 1890 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0008 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0009 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0010 | 0/0 | 1890 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0011 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0012 | 0/0 | 1890 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0013 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0014 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
t0015 | 0/0 | 1890 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/1 | 50 | 2 | 10 | 28 | 1 | 7 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0002 | 0/0 | 43 | 0 | 13 | 22 | 3 | 5 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0003 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0005 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0016 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1425 | 121 | 5 | 28 | 65 | 5 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0002 | 0/0 | 1425 | 101 | 11 | 23 | 45 | 6 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0003 | 0/0 | 1425 | 56 | 45 | 6 | 0 | 2 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0009 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0011 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0012 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0013 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0002c0004 | 0/0 | 1425 | 16 | 0 | 1 | 15 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0003c0005 | 0/0 | 1425 | 13 | 7 | 2 | 0 | 1 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0004c0006 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0005c0007 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0006c0008 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0007c0010 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0001t0002 | 1/1 | 3314 | 110 | 4 | 24 | 60 | 4 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0001t0004 | 0/0 | 3314 | 5 | 0 | 4 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0001t0005 | 0/0 | 3314 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0001t0013 | 0/0 | 3302 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0001t0014 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0002t0001 | 0/0 | 3314 | 99 | 10 | 23 | 45 | 5 | 16 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0002t0002 | 0/0 | 3314 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0002t0012 | 0/0 | 3314 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0003t0001 | 0/0 | 3314 | 49 | 40 | 4 | 0 | 2 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0003t0003 | 0/0 | 3314 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0003t0009 | 0/0 | 3314 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0003t0015 | 0/0 | 3314 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0009t0002 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0009t0005 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0011t0010 | 0/0 | 3314 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0012t0011 | 0/0 | 3314 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0001c0013t0001 | 0/0 | 3314 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0002c0004t0001 | 0/0 | 3314 | 16 | 0 | 1 | 15 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0003c0005t0001 | 0/0 | 3314 | 13 | 7 | 2 | 0 | 1 | 3 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0004c0006t0007 | 0/0 | 3314 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0005c0007t0001 | 0/0 | 3314 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0006c0008t0006 | 0/0 | 3314 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
a0007c0010t0008 | 0/0 | 3314 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | copy fasta | chr7 | 99885403 | 99924530 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0001 | 1/1 | 50 | 2 | 10 | 28 | 1 | 7 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0004g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0005g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0001t0014g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0002 | 0/0 | 43 | 0 | 13 | 22 | 3 | 5 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0002t0012g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0003 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0016 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0003g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0003t0015g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0009t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0009t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0011t0010g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0012t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0001c0013t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0002c0004t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0002c0004t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0002c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0002c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0002c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0003c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0004c0006t0007g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0005c0007t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0005c0007t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0006c0008t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0006c0008t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
a0007c0010t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0005 | t0001 | g0022 | EUR | GBR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | GBR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | FIN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0061 | EUR | FIN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00408 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00639 | hp1 | a0003 | c0005 | t0001 | g0022 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01109 | hp1 | a0001 | c0003 | t0015 | g0050 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0118 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01175 | hp2 | a0003 | c0005 | t0001 | g0022 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01243 | hp1 | a0001 | c0003 | t0003 | g0017 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0057 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0016 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0016 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0042 | EUR | IBS | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01884 | hp2 | a0003 | c0005 | t0001 | g0082 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01934 | hp1 | a0002 | c0004 | t0001 | g0055 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02071 | hp2 | a0007 | c0010 | t0008 | g0045 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02258 | hp2 | a0001 | c0003 | t0003 | g0017 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02615 | hp1 | a0001 | c0003 | t0009 | g0053 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0123 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02647 | hp1 | a0001 | c0001 | t0013 | g0048 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02723 | hp1 | a0003 | c0005 | t0001 | g0036 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02809 | hp2 | a0006 | c0008 | t0006 | g0052 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02895 | hp1 | a0004 | c0006 | t0007 | g0018 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02896 | hp1 | a0005 | c0007 | t0001 | g0035 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02897 | hp1 | a0005 | c0007 | t0001 | g0035 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02897 | hp2 | a0004 | c0006 | t0007 | g0018 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02965 | hp1 | a0003 | c0005 | t0001 | g0034 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02965 | hp2 | a0001 | c0003 | t0003 | g0017 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02970 | hp2 | a0006 | c0008 | t0006 | g0026 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0043 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03041 | hp2 | a0004 | c0006 | t0007 | g0018 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03098 | hp2 | a0001 | c0012 | t0011 | g0047 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03139 | hp2 | a0005 | c0007 | t0001 | g0085 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0044 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03225 | hp1 | a0001 | c0003 | t0003 | g0130 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03486 | hp1 | a0003 | c0005 | t0001 | g0117 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03486 | hp2 | a0001 | c0003 | t0003 | g0017 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03579 | hp2 | a0003 | c0005 | t0001 | g0080 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03669 | hp1 | a0003 | c0005 | t0001 | g0036 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0016 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03710 | hp2 | a0001 | c0013 | t0001 | g0058 | SAS | PJL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0016 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04115 | hp2 | a0003 | c0005 | t0001 | g0086 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0122 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04199 | hp2 | a0001 | c0011 | t0010 | g0046 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG04228 | hp2 | a0003 | c0005 | t0001 | g0087 | SAS | STU | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18612 | hp1 | a0001 | c0009 | t0005 | g0133 | EAS | CHB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18951 | hp2 | a0002 | c0004 | t0001 | g0031 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18954 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18956 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18964 | hp1 | a0001 | c0001 | t0014 | g0091 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18966 | hp2 | a0001 | c0009 | t0002 | g0134 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18969 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18972 | hp2 | a0002 | c0004 | t0001 | g0067 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18985 | hp1 | a0002 | c0004 | t0001 | g0068 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18986 | hp2 | a0002 | c0004 | t0001 | g0031 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18992 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | LWK | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | LWK | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19065 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19066 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19070 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19072 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19078 | hp2 | a0002 | c0004 | t0001 | g0129 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0028 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | GIH | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0131 | SAS | GIH | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02486 | hp2 | a0003 | c0005 | t0001 | g0034 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0127 | AFR | ACB | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG03471 | hp2 | a0003 | c0005 | t0001 | g0079 | AFR | MSL | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG06807 | hp1 | a0001 | c0002 | t0012 | g0083 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
HG06807 | hp2 | a0006 | c0008 | t0006 | g0026 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | TRIM4_chr7_99885403_99924530 | TRIM4 | chr7 | 99885403 | 99924530 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99892234
|
G | A | 1 | a0002 | 16 | HG00408.hp2 HG01934.hp1 NA18951.hp2 others(13): Show |
missense_variant | MODERATE | c.1354C>T | p.Arg452Cys | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1483/3314 | 1354/1425 | 452/474 | chr7 | 99892234 | ||
chr7:99892245
|
G | C | 1 | a0003 | 13 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(10): Show |
missense_variant | MODERATE | c.1343C>G | p.Ser448Cys | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1472/3314 | 1343/1425 | 448/474 | chr7 | 99892245 | ||
chr7:99892567
|
G | A | 2 | a0003a0005 | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
missense_variant | MODERATE | c.1021C>T | p.Pro341Ser | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1150/3314 | 1021/1425 | 341/474 | chr7 | 99892567 | ||
chr7:99903241
|
T | G | 1 | a0006 | 3 | HG02809.hp2 HG02970.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.818A>C | p.Lys273Thr | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 947/3314 | 818/1425 | 273/474 | chr7 | 99903241 | ||
chr7:99903303
|
C | G | 1 | a0004 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
missense_variant | MODERATE | c.756G>C | p.Gln252His | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 885/3314 | 756/1425 | 252/474 | chr7 | 99903303 | ||
chr7:99919265
|
G | T | 1 | a0007 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.137C>A | p.Pro46Gln | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/6 | 266/3314 | 137/1425 | 46/474 | chr7 | 99919265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99892463
|
G | T | 1 | a0004c0006 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.1125C>A | p.Val375Val | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1254/3314 | 1125/1425 | 375/474 | chr7 | 99892463 | ||
chr7:99903276
|
T | C | 5 | a0001c0002a0001c0011a0001c0013others(2): Show | 120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
synonymous_variant | LOW | c.783A>G | p.Val261Val | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 912/3314 | 783/1425 | 261/474 | chr7 | 99903276 | ||
chr7:99903288
|
A | G | 11 | a0001c0002a0001c0003a0001c0011others(8): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
synonymous_variant | LOW | c.771T>C | p.Ser257Ser | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/6 | 900/3314 | 771/1425 | 257/474 | chr7 | 99903288 | ||
chr7:99908681
|
A | G | 1 | a0001c0012 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.621T>C | p.Asn207Asn | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/6 | 750/3314 | 621/1425 | 207/474 | chr7 | 99908681 | ||
chr7:99909628
|
C | A | 1 | a0001c0013 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.426G>T | p.Val142Val | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/6 | 555/3314 | 426/1425 | 142/474 | chr7 | 99909628 | ||
chr7:99919108
|
G | A | 1 | a0001c0009 | 2 | NA18612.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.294C>T | p.Cys98Cys | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/6 | 423/3314 | 294/1425 | 98/474 | chr7 | 99919108 | ||
chr7:99919264
|
C | T | 1 | a0001c0011 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.138G>A | p.Pro46Pro | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/6 | 267/3314 | 138/1425 | 46/474 | chr7 | 99919264 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99890679
|
TGGACACA others(5): Show |
T | 1 | a0001c0001t0013 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472_*1483delTTTT others(8): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1472 | chr7 | 99890679 | |||||
chr7:99890920
|
C | T | 16 | a0001c0001t0001a0001c0002t0001a0001c0002t0012others(13): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1243G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1243 | chr7 | 99890920 | |||||
chr7:99890957
|
G | A | 1 | a0001c0012t0011 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1206 | chr7 | 99890957 | |||||
chr7:99890980
|
T | C | 1 | a0001c0001t0014 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1183A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1183 | chr7 | 99890980 | |||||
chr7:99890987
|
A | G | 1 | a0001c0011t0010 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1176T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1176 | chr7 | 99890987 | |||||
chr7:99890994
|
A | T | 2 | a0001c0003t0009a0006c0008t0006 | 4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1169T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1169 | chr7 | 99890994 | |||||
chr7:99891122
|
G | A | 1 | a0001c0002t0012 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1041C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1041 | chr7 | 99891122 | |||||
chr7:99891134
|
C | T | 1 | a0001c0003t0003 | 5 | HG01243.hp1 HG02258.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1029G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 1029 | chr7 | 99891134 | |||||
chr7:99891275
|
C | A | 1 | a0004c0006t0007 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*888G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 888 | chr7 | 99891275 | |||||
chr7:99891317
|
A | T | 16 | a0001c0001t0001a0001c0002t0001a0001c0002t0012others(13): Show | 199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*846T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 846 | chr7 | 99891317 | |||||
chr7:99891382
|
A | G | 17 | a0001c0001t0001a0001c0001t0013a0001c0002t0001others(14): Show | 200 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*781T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 781 | chr7 | 99891382 | |||||
chr7:99891395
|
G | A | 1 | a0001c0003t0015 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 768 | chr7 | 99891395 | |||||
chr7:99891607
|
A | G | 2 | a0001c0001t0005a0001c0009t0005 | 4 | HG02040.hp1 HG02080.hp1 NA18612.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*556T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 556 | chr7 | 99891607 | |||||
chr7:99891827
|
C | T | 1 | a0001c0003t0009 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*336G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 336 | chr7 | 99891827 | |||||
chr7:99891948
|
G | A | 1 | a0001c0001t0004 | 5 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*215C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 215 | chr7 | 99891948 | |||||
chr7:99892138
|
A | T | 1 | a0007c0010t0008 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 6/6 | 25 | chr7 | 99892138 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:99892878
|
T | A | 22 | a0001c0003t0001g0003a0001c0003t0001g0010a0001c0003t0001g0014others(19): Show | 53 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.842-132A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99892878 | ||||||
chr7:99893110
|
C | A | 1 | a0001c0002t0001g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.842-364G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893110 | ||||||
chr7:99893117
|
A | G | 1 | a0001c0003t0001g0024 | 3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.842-371T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893117 | ||||||
chr7:99893333
|
A | T | 88 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(85): Show | 198 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.842-587T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893333 | ||||||
chr7:99893368
|
C | CAT | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-623_842-622ins others(2): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893368 | ||||||
chr7:99893370
|
C | CAT | 78 | a0001c0001t0013g0048a0001c0002t0001g0002a0001c0002t0001g0005others(75): Show | 183 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.842-625_842-624ins others(2): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893370 | ||||||
chr7:99893370
|
C | T | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-624G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893370 | ||||||
chr7:99893432
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.842-686C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893432 | ||||||
chr7:99893455
|
A | T | 1 | a0001c0012t0011g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.842-709T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893455 | ||||||
chr7:99893623
|
T | A | 1 | a0001c0002t0001g0062 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.842-877A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893623 | ||||||
chr7:99893695
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.842-949A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893695 | ||||||
chr7:99893715
|
T | C | 1 | a0001c0012t0011g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.842-969A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893715 | ||||||
chr7:99893967
|
C | CT | 12 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0040others(9): Show | 23 | HG00408.hp1 HG00738.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.842-1222dupA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893967 | ||||||
chr7:99893967
|
C | CTT | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-1223_842-1222d others(4): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99893967 | ||||||
chr7:99894414
|
C | T | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.842-1668G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894414 | ||||||
chr7:99894430
|
C | T | 3 | a0001c0002t0001g0060a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG02976.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.842-1684G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894430 | ||||||
chr7:99894538
|
G | A | 2 | a0002c0004t0001g0031a0002c0004t0001g0129 | 3 | NA18951.hp2 NA18986.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.842-1792C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894538 | ||||||
chr7:99894637
|
A | C | 1 | a0001c0002t0001g0030 | 2 | HG01928.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.842-1891T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894637 | ||||||
chr7:99894670
|
C | G | 1 | a0001c0001t0002g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.842-1924G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894670 | ||||||
chr7:99894673
|
A | C | 76 | a0001c0001t0002g0094a0001c0002t0001g0002a0001c0002t0001g0005others(73): Show | 179 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-1927T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894673 | ||||||
chr7:99894674
|
A | C | 1 | a0001c0003t0001g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.842-1928T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99894674 | ||||||
chr7:99895082
|
A | T | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.842-2336T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895082 | ||||||
chr7:99895133
|
A | G | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-2387T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895133 | ||||||
chr7:99895493
|
C | T | 1 | a0001c0001t0002g0038 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.842-2747G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895493 | ||||||
chr7:99895536
|
T | A | 1 | a0001c0003t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.842-2790A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895536 | ||||||
chr7:99895647
|
G | C | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-2901C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895647 | ||||||
chr7:99895809
|
T | G | 1 | a0004c0006t0007g0018 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.842-3063A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895809 | ||||||
chr7:99895849
|
T | C | 1 | a0001c0001t0013g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.842-3103A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99895849 | ||||||
chr7:99896037
|
G | A | 22 | a0001c0003t0001g0003a0001c0003t0001g0010a0001c0003t0001g0014others(19): Show | 53 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.842-3291C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896037 | ||||||
chr7:99896187
|
T | C | 1 | a0001c0002t0001g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.842-3441A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896187 | ||||||
chr7:99896188
|
G | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-3442C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896188 | ||||||
chr7:99896257
|
G | C | 52 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(49): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.842-3511C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896257 | ||||||
chr7:99896312
|
G | T | 1 | a0001c0003t0001g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.842-3566C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896312 | ||||||
chr7:99896407
|
G | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-3661C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896407 | ||||||
chr7:99896609
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.842-3863C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896609 | ||||||
chr7:99896774
|
C | T | 1 | a0001c0002t0001g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.842-4028G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896774 | ||||||
chr7:99896840
|
A | C | 1 | a0001c0001t0002g0103 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.842-4094T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896840 | ||||||
chr7:99896882
|
C | T | 5 | a0001c0003t0001g0015a0001c0003t0001g0025a0001c0003t0001g0043others(2): Show | 11 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.842-4136G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896882 | ||||||
chr7:99896890
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.842-4144G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896890 | ||||||
chr7:99896916
|
A | G | 1 | a0001c0003t0009g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.842-4170T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896916 | ||||||
chr7:99896944
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.842-4198C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896944 | ||||||
chr7:99896972
|
T | C | 2 | a0001c0001t0002g0040a0001c0001t0002g0103 | 3 | HG01358.hp2 HG01943.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.842-4226A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896972 | ||||||
chr7:99896985
|
A | G | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-4239T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99896985 | ||||||
chr7:99897057
|
T | C | 1 | a0001c0001t0013g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.842-4311A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99897057 | ||||||
chr7:99897849
|
T | G | 52 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(49): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.842-5103A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99897849 | ||||||
chr7:99897936
|
C | G | 1 | a0001c0001t0002g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.842-5190G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99897936 | ||||||
chr7:99898109
|
A | G | 2 | a0001c0001t0004g0012a0001c0001t0004g0098 | 5 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.841+5109T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898109 | ||||||
chr7:99898119
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.841+5099G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898119 | ||||||
chr7:99898208
|
A | G | 2 | a0006c0008t0006g0026a0006c0008t0006g0052 | 3 | HG02809.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.841+5010T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898208 | ||||||
chr7:99898310
|
C | T | 2 | a0001c0012t0011g0047a0004c0006t0007g0018 | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.841+4908G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898310 | ||||||
chr7:99898369
|
C | T | 1 | a0004c0006t0007g0018 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.841+4849G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898369 | ||||||
chr7:99898418
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.841+4800C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898418 | ||||||
chr7:99898532
|
C | G | 1 | a0001c0001t0002g0006 | 6 | HG00423.hp1 HG00673.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+4686G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898532 | ||||||
chr7:99898554
|
G | A | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+4664C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898554 | ||||||
chr7:99898860
|
A | G | 1 | a0001c0001t0004g0098 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.841+4358T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99898860 | ||||||
chr7:99899044
|
G | A | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+4174C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899044 | ||||||
chr7:99899118
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.841+4100G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899118 | ||||||
chr7:99899137
|
C | G | 1 | a0001c0003t0001g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.841+4081G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899137 | ||||||
chr7:99899156
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.841+4062T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899156 | ||||||
chr7:99899391
|
T | C | 1 | a0007c0010t0008g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.841+3827A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899391 | ||||||
chr7:99899644
|
A | G | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+3574T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899644 | ||||||
chr7:99899699
|
C | T | 2 | a0001c0002t0001g0072a0001c0002t0001g0074 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.841+3519G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899699 | ||||||
chr7:99899878
|
C | A | 4 | a0001c0003t0001g0044a0001c0003t0001g0119a0001c0003t0001g0125others(1): Show | 5 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.841+3340G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899878 | ||||||
chr7:99899941
|
C | T | 1 | a0002c0004t0001g0055 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.841+3277G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899941 | ||||||
chr7:99899978
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.841+3240C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99899978 | ||||||
chr7:99900080
|
C | G | 1 | a0001c0003t0001g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841+3138G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900080 | ||||||
chr7:99900334
|
T | A | 76 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(73): Show | 179 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+2884A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900334 | ||||||
chr7:99900395
|
A | C | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.841+2823T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900395 | ||||||
chr7:99900522
|
G | A | 90 | a0001c0001t0013g0048a0001c0002t0001g0002a0001c0002t0001g0005others(87): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.841+2696C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900522 | ||||||
chr7:99900709
|
A | AT | 52 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(49): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.841+2508dupA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900709 | ||||||
chr7:99900876
|
A | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.841+2342T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900876 | ||||||
chr7:99900918
|
T | A | 1 | a0001c0003t0009g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.841+2300A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900918 | ||||||
chr7:99900929
|
C | CTCAGGGT others(4): Show |
46 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(43): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.841+2288_841+2289i others(13): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900929 | ||||||
chr7:99900934
|
A | ATTTCT | 46 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(43): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.841+2283_841+2284i others(7): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99900934 | ||||||
chr7:99901105
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.841+2113C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901105 | ||||||
chr7:99901290
|
G | A | 2 | a0001c0012t0011g0047a0004c0006t0007g0018 | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.841+1928C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901290 | ||||||
chr7:99901388
|
G | A | 1 | a0004c0006t0007g0018 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.841+1830C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901388 | ||||||
chr7:99901442
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.841+1776T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901442 | ||||||
chr7:99901486
|
T | C | 1 | a0001c0003t0015g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.841+1732A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901486 | ||||||
chr7:99901583
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.841+1635A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901583 | ||||||
chr7:99901733
|
G | A | 1 | a0003c0005t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.841+1485C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99901733 | ||||||
chr7:99902176
|
T | C | 1 | a0001c0001t0002g0013 | 4 | HG00738.hp1 HG01175.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+1042A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902176 | ||||||
chr7:99902249
|
A | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.841+969T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902249 | ||||||
chr7:99902419
|
T | G | 49 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(46): Show | 120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.841+799A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902419 | ||||||
chr7:99902631
|
G | A | 2 | a0001c0002t0001g0064a0001c0002t0001g0071 | 2 | HG03017.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.841+587C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902631 | ||||||
chr7:99902700
|
C | G | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+518G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902700 | ||||||
chr7:99902782
|
T | G | 1 | a0001c0003t0015g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.841+436A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902782 | ||||||
chr7:99902889
|
C | A | 1 | a0001c0002t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.841+329G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902889 | ||||||
chr7:99902974
|
G | A | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.841+244C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 5/5 | chr7 | 99902974 | ||||||
chr7:99903343
|
G | A | 1 | a0001c0001t0002g0113 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.744-28C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903343 | ||||||
chr7:99903391
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.744-76T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903391 | ||||||
chr7:99903463
|
C | T | 1 | a0001c0003t0001g0044 | 2 | HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.743+113G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903463 | ||||||
chr7:99903566
|
G | A | 1 | a0001c0003t0015g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.743+10C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 4/5 | chr7 | 99903566 | ||||||
chr7:99903690
|
A | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.721-92T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903690 | ||||||
chr7:99903752
|
T | C | 3 | a0003c0005t0001g0034a0003c0005t0001g0082a0003c0005t0001g0117 | 4 | HG01884.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-154A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903752 | ||||||
chr7:99903853
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.721-255G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903853 | ||||||
chr7:99903899
|
C | T | 1 | a0001c0003t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.721-301G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99903899 | ||||||
chr7:99904204
|
T | C | 1 | a0001c0003t0001g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.721-606A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904204 | ||||||
chr7:99904245
|
G | A | 1 | a0004c0006t0007g0018 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.721-647C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904245 | ||||||
chr7:99904351
|
A | T | 3 | a0001c0003t0009g0053a0006c0008t0006g0026a0006c0008t0006g0052 | 4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-753T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904351 | ||||||
chr7:99904488
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0029a0001c0002t0001g0049 | 6 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-890T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904488 | ||||||
chr7:99904790
|
G | A | 3 | a0001c0002t0001g0059a0001c0002t0001g0066a0001c0011t0010g0046 | 3 | HG02735.hp2 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.721-1192C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904790 | ||||||
chr7:99904964
|
G | A | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.721-1366C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99904964 | ||||||
chr7:99905050
|
TA | T | 67 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(64): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.721-1453delT | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905050 | ||||||
chr7:99905208
|
T | C | 1 | a0001c0003t0001g0120 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.721-1610A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905208 | ||||||
chr7:99905582
|
G | C | 1 | a0001c0003t0001g0120 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.721-1984C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905582 | ||||||
chr7:99905674
|
A | G | 2 | a0001c0001t0002g0004a0001c0001t0002g0116 | 8 | HG00408.hp1 HG02040.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-2076T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905674 | ||||||
chr7:99905687
|
A | G | 1 | a0001c0003t0009g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.721-2089T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905687 | ||||||
chr7:99905919
|
C | T | 23 | a0001c0003t0001g0003a0001c0003t0001g0010a0001c0003t0001g0014others(20): Show | 54 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(51): Show |
intron_variant | MODIFIER | c.721-2321G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905919 | ||||||
chr7:99905929
|
G | A | 1 | a0001c0002t0001g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.721-2331C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99905929 | ||||||
chr7:99906002
|
A | G | 90 | a0001c0001t0013g0048a0001c0002t0001g0002a0001c0002t0001g0005others(87): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.721-2404T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906002 | ||||||
chr7:99906100
|
G | A | 1 | a0001c0003t0009g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.720+2482C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906100 | ||||||
chr7:99906313
|
A | T | 1 | a0003c0005t0001g0082 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.720+2269T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906313 | ||||||
chr7:99906453
|
A | C | 1 | a0001c0002t0001g0019 | 3 | HG02055.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.720+2129T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906453 | ||||||
chr7:99906809
|
G | A | 1 | a0001c0003t0001g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.720+1773C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99906809 | ||||||
chr7:99907340
|
C | T | 1 | a0001c0012t0011g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.720+1242G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907340 | ||||||
chr7:99907353
|
A | C | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.720+1229T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907353 | ||||||
chr7:99907431
|
G | A | 49 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(46): Show | 120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.720+1151C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907431 | ||||||
chr7:99907483
|
T | C | 2 | a0001c0003t0001g0025a0001c0003t0001g0118 | 4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1099A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907483 | ||||||
chr7:99907600
|
G | A | 46 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(43): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.720+982C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907600 | ||||||
chr7:99907783
|
T | C | 1 | a0001c0003t0001g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.720+799A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907783 | ||||||
chr7:99907787
|
A | C | 1 | a0006c0008t0006g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.720+795T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907787 | ||||||
chr7:99907857
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.720+725G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907857 | ||||||
chr7:99907996
|
G | A | 2 | a0006c0008t0006g0026a0006c0008t0006g0052 | 3 | HG02809.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.720+586C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99907996 | ||||||
chr7:99908027
|
G | A | 1 | a0001c0002t0001g0057 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.720+555C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908027 | ||||||
chr7:99908268
|
T | C | 1 | a0001c0002t0001g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.720+314A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908268 | ||||||
chr7:99908282
|
T | C | 4 | a0001c0012t0011g0047a0004c0006t0007g0018a0005c0007t0001g0035others(1): Show | 7 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+300A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908282 | ||||||
chr7:99908525
|
G | C | 2 | a0001c0003t0001g0016a0001c0003t0001g0122 | 5 | HG01516.hp2 HG01517.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+57C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 3/5 | chr7 | 99908525 | ||||||
chr7:99908920
|
G | A | 3 | a0003c0005t0001g0034a0003c0005t0001g0082a0003c0005t0001g0117 | 4 | HG01884.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-108C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99908920 | ||||||
chr7:99908960
|
C | G | 1 | a0001c0002t0001g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-148G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99908960 | ||||||
chr7:99909133
|
G | GGT | 7 | a0001c0001t0013g0048a0001c0002t0001g0072a0001c0002t0001g0073others(4): Show | 10 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-323_490-322dup others(2): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | ||||||
chr7:99909133
|
G | GGTGT | 21 | a0001c0002t0001g0020a0001c0002t0001g0033a0001c0002t0001g0070others(18): Show | 33 | HG00408.hp2 HG01109.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.490-325_490-322dup others(4): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | ||||||
chr7:99909133
|
G | GGTGTGT | 11 | a0001c0002t0001g0005a0001c0002t0001g0021a0001c0002t0001g0069others(8): Show | 24 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.490-327_490-322dup others(6): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | ||||||
chr7:99909133
|
G | GGTGTGTG others(1): Show |
25 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0019others(22): Show | 75 | HG00099.hp2 HG00280.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-329_490-322dup others(8): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | ||||||
chr7:99909133
|
G | GGTGTGTG others(3): Show |
1 | a0001c0002t0001g0028 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.490-331_490-322dup others(10): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | ||||||
chr7:99909133
|
G | GGTGTGTG others(5): Show |
1 | a0001c0002t0001g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.490-333_490-322dup others(12): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909133 | ||||||
chr7:99909157
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.490-345A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909157 | ||||||
chr7:99909157
|
T | TGTGC | 1 | a0003c0005t0001g0022 | 3 | HG00099.hp1 HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.490-346_490-345ins others(4): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909157 | ||||||
chr7:99909159
|
C | T | 1 | a0001c0002t0001g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.490-347G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909159 | ||||||
chr7:99909177
|
T | G | 2 | a0001c0003t0001g0016a0001c0003t0001g0122 | 5 | HG01516.hp2 HG01517.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-365A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909177 | ||||||
chr7:99909358
|
C | A | 1 | a0006c0008t0006g0026 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.489+207G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909358 | ||||||
chr7:99909360
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.489+205C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 2/5 | chr7 | 99909360 | ||||||
chr7:99909729
|
GT | G | 71 | a0001c0001t0002g0041a0001c0001t0002g0107a0001c0001t0002g0110others(68): Show | 174 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.394-70delA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909729 | ||||||
chr7:99909729
|
GTT | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0003c0005t0001g0022others(7): Show | 14 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-71_394-70delAA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909729 | ||||||
chr7:99909730
|
T | G | 8 | a0001c0002t0001g0027a0001c0002t0001g0056a0001c0002t0001g0057others(5): Show | 9 | HG01361.hp2 HG01516.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-70A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909730 | ||||||
chr7:99909731
|
T | G | 67 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(64): Show | 169 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.394-71A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909731 | ||||||
chr7:99909732
|
T | G | 10 | a0001c0002t0001g0076a0001c0002t0001g0077a0003c0005t0001g0022others(7): Show | 14 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-72A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909732 | ||||||
chr7:99909733
|
T | G | 2 | a0001c0012t0011g0047a0004c0006t0007g0018 | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-73A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909733 | ||||||
chr7:99909734
|
T | G | 3 | a0001c0001t0002g0108a0005c0007t0001g0035a0005c0007t0001g0085 | 4 | HG02896.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-74A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909734 | ||||||
chr7:99909736
|
T | G | 1 | a0001c0001t0002g0109 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.394-76A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99909736 | ||||||
chr7:99910037
|
ATTT | A | 9 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(6): Show | 13 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-380_394-378del others(3): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910037 | ||||||
chr7:99910318
|
C | T | 1 | a0003c0005t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394-658G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910318 | ||||||
chr7:99910570
|
C | T | 1 | a0001c0003t0001g0119 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.394-910G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910570 | ||||||
chr7:99910716
|
G | T | 1 | a0001c0003t0001g0119 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.394-1056C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910716 | ||||||
chr7:99910802
|
T | C | 2 | a0001c0003t0003g0017a0001c0003t0003g0130 | 5 | HG01243.hp1 HG02258.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-1142A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99910802 | ||||||
chr7:99911028
|
T | C | 11 | a0003c0005t0001g0022a0003c0005t0001g0034a0003c0005t0001g0036others(8): Show | 16 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.394-1368A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911028 | ||||||
chr7:99911118
|
A | G | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-1458T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911118 | ||||||
chr7:99911384
|
G | A | 1 | a0001c0012t0011g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394-1724C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911384 | ||||||
chr7:99911701
|
C | T | 49 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(46): Show | 120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.394-2041G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911701 | ||||||
chr7:99911952
|
C | G | 1 | a0001c0012t0011g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394-2292G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99911952 | ||||||
chr7:99912315
|
G | A | 1 | a0001c0001t0013g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-2655C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912315 | ||||||
chr7:99912530
|
T | TC | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-2871_394-2870i others(3): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912530 | ||||||
chr7:99912531
|
T | A | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-2871A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912531 | ||||||
chr7:99912531
|
T | TA | 81 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(78): Show | 187 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.394-2872dupT | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912531 | ||||||
chr7:99912541
|
A | T | 1 | a0001c0001t0005g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-2881T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912541 | ||||||
chr7:99912543
|
AT | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0110 | 3 | HG01515.hp2 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.394-2884delA | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912543 | ||||||
chr7:99912544
|
T | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.394-2884A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912544 | ||||||
chr7:99912611
|
A | C | 52 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(49): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.394-2951T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912611 | ||||||
chr7:99912620
|
G | T | 3 | a0001c0001t0001g0090a0001c0001t0002g0092a0001c0001t0014g0091 | 3 | NA18964.hp1 NA18988.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.394-2960C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912620 | ||||||
chr7:99912656
|
G | A | 1 | a0001c0003t0009g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.394-2996C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912656 | ||||||
chr7:99912892
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.394-3232T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99912892 | ||||||
chr7:99913227
|
T | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.394-3567A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913227 | ||||||
chr7:99913248
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.394-3588C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913248 | ||||||
chr7:99913438
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.394-3778C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913438 | ||||||
chr7:99913594
|
C | T | 1 | a0003c0005t0001g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.394-3934G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913594 | ||||||
chr7:99913596
|
G | A | 1 | a0001c0001t0002g0112 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.394-3936C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913596 | ||||||
chr7:99913628
|
G | A | 1 | a0001c0002t0001g0021 | 3 | HG00423.hp2 NA18941.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.394-3968C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913628 | ||||||
chr7:99913661
|
A | T | 1 | a0006c0008t0006g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394-4001T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913661 | ||||||
chr7:99913670
|
C | CAAAT | 47 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(44): Show | 115 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.394-4014_394-4011d others(6): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913670 | ||||||
chr7:99913670
|
C | CAAATAAA others(1): Show |
6 | a0001c0002t0001g0054a0001c0003t0009g0053a0001c0003t0015g0050others(3): Show | 10 | HG01109.hp1 HG01433.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-4018_394-4011d others(10): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913670 | ||||||
chr7:99913723
|
T | C | 1 | a0001c0002t0001g0033 | 2 | NA18948.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.394-4063A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913723 | ||||||
chr7:99913749
|
A | G | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.394-4089T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913749 | ||||||
chr7:99913940
|
A | T | 49 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(46): Show | 120 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.394-4280T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99913940 | ||||||
chr7:99914000
|
C | T | 1 | a0001c0001t0013g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-4340G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914000 | ||||||
chr7:99914086
|
C | A | 1 | a0001c0002t0001g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-4426G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914086 | ||||||
chr7:99914102
|
C | T | 3 | a0003c0005t0001g0034a0003c0005t0001g0082a0003c0005t0001g0117 | 4 | HG01884.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-4442G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914102 | ||||||
chr7:99914243
|
G | A | 2 | a0003c0005t0001g0034a0003c0005t0001g0082 | 3 | HG01884.hp2 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.394-4583C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914243 | ||||||
chr7:99914405
|
C | T | 3 | a0001c0003t0009g0053a0006c0008t0006g0026a0006c0008t0006g0052 | 4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+4604G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914405 | ||||||
chr7:99914601
|
G | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(86): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.393+4408C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914601 | ||||||
chr7:99914712
|
G | A | 1 | a0007c0010t0008g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.393+4297C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914712 | ||||||
chr7:99914965
|
G | A | 1 | a0001c0002t0012g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.393+4044C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99914965 | ||||||
chr7:99915000
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.393+4009C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915000 | ||||||
chr7:99915123
|
T | C | 1 | a0001c0003t0015g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+3886A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915123 | ||||||
chr7:99915316
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.393+3693T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915316 | ||||||
chr7:99915504
|
T | C | 2 | a0005c0007t0001g0035a0005c0007t0001g0085 | 3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.393+3505A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915504 | ||||||
chr7:99915609
|
G | C | 1 | a0004c0006t0007g0018 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.393+3400C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99915609 | ||||||
chr7:99916064
|
G | A | 1 | a0001c0003t0015g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+2945C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916064 | ||||||
chr7:99916246
|
T | G | 1 | a0001c0001t0002g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.393+2763A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916246 | ||||||
chr7:99916375
|
C | A | 1 | a0001c0001t0002g0113 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.393+2634G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916375 | ||||||
chr7:99916474
|
T | C | 4 | a0003c0005t0001g0022a0003c0005t0001g0036a0003c0005t0001g0086others(1): Show | 7 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+2535A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916474 | ||||||
chr7:99916758
|
C | G | 1 | a0001c0001t0002g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.393+2251G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916758 | ||||||
chr7:99916794
|
A | C | 88 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0011others(85): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.393+2215T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916794 | ||||||
chr7:99916883
|
A | T | 1 | a0001c0001t0002g0088 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.393+2126T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916883 | ||||||
chr7:99916963
|
A | G | 1 | a0001c0003t0001g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.393+2046T>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99916963 | ||||||
chr7:99917024
|
A | T | 1 | a0001c0001t0002g0037 | 2 | HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.393+1985T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917024 | ||||||
chr7:99917476
|
T | C | 1 | a0001c0001t0002g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.393+1533A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917476 | ||||||
chr7:99917477
|
T | C | 90 | a0001c0001t0013g0048a0001c0002t0001g0002a0001c0002t0001g0005others(87): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.393+1532A>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917477 | ||||||
chr7:99917478
|
G | A | 1 | a0003c0005t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.393+1531C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917478 | ||||||
chr7:99917513
|
A | C | 1 | a0001c0003t0015g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+1496T>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917513 | ||||||
chr7:99917517
|
C | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1492G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917517 | ||||||
chr7:99917518
|
G | GATGGGGG others(100): Show |
1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1490_393+1491i others(109): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917518 | ||||||
chr7:99917522
|
C | T | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1487G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917522 | ||||||
chr7:99917523
|
C | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1486G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917523 | ||||||
chr7:99917531
|
C | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1478G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917531 | ||||||
chr7:99917532
|
C | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1477G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917532 | ||||||
chr7:99917535
|
C | G | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1474G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917535 | ||||||
chr7:99917537
|
T | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1472A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917537 | ||||||
chr7:99917540
|
T | G | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1469A>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917540 | ||||||
chr7:99917544
|
ACCCTGTC others(3): Show |
A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1455_393+1464d others(12): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917544 | ||||||
chr7:99917556
|
C | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1453G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917556 | ||||||
chr7:99917557
|
T | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1452A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917557 | ||||||
chr7:99917563
|
T | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1446A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917563 | ||||||
chr7:99917565
|
C | G | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1444G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917565 | ||||||
chr7:99917569
|
ATTAGCTG others(86): Show |
A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1347_393+1439d others(95): Show |
TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917569 | ||||||
chr7:99917663
|
G | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1346C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917663 | ||||||
chr7:99917666
|
T | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1343A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917666 | ||||||
chr7:99917667
|
T | A | 1 | a0001c0003t0003g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.393+1342A>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917667 | ||||||
chr7:99917677
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.393+1332G>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917677 | ||||||
chr7:99917690
|
G | T | 1 | a0001c0001t0013g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.393+1319C>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917690 | ||||||
chr7:99917772
|
T | TG | 2 | a0001c0001t0002g0023a0001c0001t0002g0115 | 4 | NA18985.hp2 NA18992.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+1236dupC | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99917772 | ||||||
chr7:99918040
|
G | C | 1 | a0001c0001t0002g0116 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.393+969C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918040 | ||||||
chr7:99918359
|
C | G | 90 | a0001c0001t0013g0048a0001c0002t0001g0002a0001c0002t0001g0005others(87): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.393+650G>C | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918359 | ||||||
chr7:99918381
|
A | T | 2 | a0001c0012t0011g0047a0004c0006t0007g0018 | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+628T>A | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918381 | ||||||
chr7:99918492
|
G | C | 1 | a0003c0005t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.393+517C>G | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918492 | ||||||
chr7:99918566
|
G | GA | 23 | a0001c0003t0001g0003a0001c0003t0001g0010a0001c0003t0001g0014others(20): Show | 54 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+442dupT | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918566 | ||||||
chr7:99918725
|
G | A | 1 | a0001c0002t0001g0131 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.393+284C>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99918725 | ||||||
chr7:99919008
|
C | A | 1 | a0001c0002t0001g0132 | 1 | HG01361.hp2 | splice_donor_variant&intron_variant | HIGH | c.393+1G>T | TRIM4 | ENSG00000146833.16 | transcript | ENST00000349062.7 | protein_coding | 1/5 | chr7 | 99919008 |