geneid | 84675 |
---|---|
ensemblid | ENSG00000147573.17 |
hgncid | 14215 |
symbol | TRIM55 |
name | tripartite motif containing 55 |
refseq_nuc | NM_184085.2 |
refseq_prot | NP_908973.1 |
ensembl_nuc | ENST00000315962.9 |
ensembl_prot | ENSP00000323913.4 |
mane_status | MANE Select |
chr | chr8 |
start | 66127129 |
end | 66175485 |
strand | + |
ver | v1.2 |
region | chr8:66127129-66175485 |
region5000 | chr8:66122129-66180485 |
regionname0 | TRIM55_chr8_66127129_66175485 |
regionname5000 | TRIM55_chr8_66122129_66180485 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 548 | 178 | 27 | 40 | 76 | 12 | 21 | 48 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002 | 0/0 | 548 | 68 | 58 | 5 | 0 | 0 | 5 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0003 | 0/0 | 548 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0004 | 0/0 | 548 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1647 | 167 | 26 | 39 | 68 | 12 | 20 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0002 | 0/0 | 1647 | 30 | 27 | 2 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0003 | 0/0 | 1647 | 25 | 19 | 2 | 0 | 0 | 4 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0004 | 0/0 | 1647 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0005 | 0/0 | 1647 | 9 | 0 | 1 | 8 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0006 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0007 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0008 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0009 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0010 | 0/0 | 1647 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
c0011 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1033 | 216 | 64 | 43 | 76 | 11 | 20 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
t0002 | 0/0 | 1033 | 24 | 18 | 2 | 0 | 0 | 4 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
t0003 | 0/0 | 1033 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
t0004 | 0/0 | 1033 | 3 | 0 | 1 | 0 | 1 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
t0005 | 0/0 | 1033 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0002 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0012 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1647 | 167 | 26 | 39 | 68 | 12 | 20 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0005 | 0/0 | 1647 | 9 | 0 | 1 | 8 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0010 | 0/0 | 1647 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0011 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0002 | 0/0 | 1647 | 30 | 27 | 2 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0003 | 0/0 | 1647 | 25 | 19 | 2 | 0 | 0 | 4 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0004 | 0/0 | 1647 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0006 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0008 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0003c0009 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0004c0007 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2679 | 163 | 26 | 38 | 68 | 11 | 18 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0001t0004 | 0/0 | 2679 | 3 | 0 | 1 | 0 | 1 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0001t0005 | 0/0 | 2679 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0005t0001 | 0/0 | 2679 | 9 | 0 | 1 | 8 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0010t0001 | 0/0 | 2679 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0001c0011t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0002t0001 | 0/0 | 2679 | 22 | 19 | 2 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0002t0002 | 0/0 | 2679 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0002t0003 | 0/0 | 2679 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0003t0001 | 0/0 | 2679 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0003t0002 | 0/0 | 2679 | 20 | 14 | 2 | 0 | 0 | 4 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0004t0001 | 0/0 | 2679 | 10 | 10 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0006t0001 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0002c0008t0001 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0003c0009t0001 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
a0004c0007t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | copy fasta | chr8 | 66122129 | 66180485 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0012 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0010t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0001c0011t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0006t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0002c0008t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0003c0009t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
a0004c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | GBR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00438 | hp2 | a0001 | c0005 | t0001 | g0155 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00544 | hp2 | a0001 | c0005 | t0001 | g0157 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00609 | hp2 | a0001 | c0005 | t0001 | g0158 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00639 | hp2 | a0002 | c0003 | t0002 | g0005 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01167 | hp2 | a0002 | c0008 | t0001 | g0050 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0021 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0128 | EUR | IBS | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01943 | hp1 | a0001 | c0005 | t0001 | g0160 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02004 | hp2 | a0003 | c0009 | t0001 | g0043 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02055 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02056 | hp1 | a0001 | c0005 | t0001 | g0170 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02074 | hp1 | a0001 | c0005 | t0001 | g0159 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02145 | hp1 | a0002 | c0004 | t0001 | g0218 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02145 | hp2 | a0002 | c0002 | t0003 | g0032 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0061 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0059 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02572 | hp2 | a0002 | c0004 | t0001 | g0219 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02622 | hp1 | a0002 | c0004 | t0001 | g0222 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02622 | hp2 | a0002 | c0003 | t0002 | g0004 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02630 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02647 | hp2 | a0002 | c0004 | t0001 | g0220 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02717 | hp2 | a0004 | c0007 | t0001 | g0054 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02723 | hp2 | a0002 | c0003 | t0002 | g0056 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02809 | hp1 | a0002 | c0004 | t0001 | g0217 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02818 | hp1 | a0002 | c0003 | t0002 | g0058 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02818 | hp2 | a0002 | c0003 | t0002 | g0004 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02886 | hp2 | a0002 | c0006 | t0001 | g0151 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03041 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03041 | hp2 | a0002 | c0004 | t0001 | g0216 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03195 | hp1 | a0002 | c0003 | t0002 | g0018 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03209 | hp2 | a0002 | c0004 | t0001 | g0013 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0023 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03239 | hp1 | a0002 | c0003 | t0002 | g0022 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03486 | hp1 | a0002 | c0003 | t0002 | g0019 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03490 | hp1 | a0002 | c0003 | t0002 | g0006 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03492 | hp2 | a0002 | c0003 | t0002 | g0006 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0033 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03540 | hp2 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03579 | hp2 | a0002 | c0003 | t0002 | g0014 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03704 | hp2 | a0001 | c0010 | t0001 | g0153 | SAS | PJL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0231 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG04184 | hp1 | a0002 | c0003 | t0002 | g0005 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0090 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18522 | hp2 | a0002 | c0003 | t0002 | g0015 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18940 | hp1 | a0001 | c0005 | t0001 | g0062 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19030 | hp1 | a0002 | c0004 | t0001 | g0221 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19030 | hp2 | a0001 | c0011 | t0001 | g0030 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19043 | hp1 | a0002 | c0003 | t0002 | g0016 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | LWK | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19066 | hp1 | a0001 | c0005 | t0001 | g0166 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19082 | hp1 | a0001 | c0005 | t0001 | g0072 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19240 | hp1 | a0002 | c0006 | t0001 | g0119 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA19240 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | YRI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ASW | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ASW | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02559 | hp1 | a0002 | c0003 | t0002 | g0017 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG02559 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0036 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | MSL | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20300 | hp1 | a0002 | c0004 | t0001 | g0223 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
NA20300 | hp2 | a0002 | c0003 | t0002 | g0057 | AFR | USA | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0168 | REF | REF | TRIM55_chr8_66122129_66180485 | TRIM55 | chr8 | 66122129 | 66180485 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66135039
|
C | T | 1 | a0003 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.391C>T | p.Arg131Cys | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/10 | 531/2679 | 391/1647 | 131/548 | chr8 | 66135039 | ||
chr8:66149745
|
G | A | 1 | a0004 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.704G>A | p.Arg235Gln | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/10 | 844/2679 | 704/1647 | 235/548 | chr8 | 66149745 | ||
chr8:66152419
|
A | G | 3 | a0002a0003a0004 | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
missense_variant | MODERATE | c.1028A>G | p.Lys343Arg | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/10 | 1168/2679 | 1028/1647 | 343/548 | chr8 | 66152419 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66127274
|
C | T | 1 | a0001c0011 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.6C>T | p.Ser2Ser | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 146/2679 | 6/1647 | 2/548 | chr8 | 66127274 | ||
chr8:66127277
|
A | G | 1 | a0001c0010 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.9A>G | p.Ala3Ala | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 149/2679 | 9/1647 | 3/548 | chr8 | 66127277 | ||
chr8:66127370
|
G | A | 1 | a0002c0004 | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.102G>A | p.Thr34Thr | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 242/2679 | 102/1647 | 34/548 | chr8 | 66127370 | ||
chr8:66135149
|
A | G | 1 | a0002c0008 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.501A>G | p.Arg167Arg | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/10 | 641/2679 | 501/1647 | 167/548 | chr8 | 66135149 | ||
chr8:66149812
|
C | T | 1 | a0002c0006 | 2 | HG02886.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.771C>T | p.Asn257Asn | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/10 | 911/2679 | 771/1647 | 257/548 | chr8 | 66149812 | ||
chr8:66150348
|
G | A | 1 | a0002c0003 | 25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
synonymous_variant | LOW | c.867G>A | p.Ser289Ser | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/10 | 1007/2679 | 867/1647 | 289/548 | chr8 | 66150348 | ||
chr8:66152378
|
A | G | 1 | a0001c0005 | 9 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.987A>G | p.Glu329Glu | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/10 | 1127/2679 | 987/1647 | 329/548 | chr8 | 66152378 | ||
chr8:66154277
|
G | A | 1 | a0002c0004 | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.1467G>A | p.Ala489Ala | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/10 | 1607/2679 | 1467/1647 | 489/548 | chr8 | 66154277 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66127154
|
G | A | 2 | a0002c0002t0002a0002c0003t0002 | 24 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-115G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/10 | 115 | chr8 | 66127154 | |||||
chr8:66174875
|
C | T | 1 | a0001c0001t0004 | 3 | HG00735.hp2 HG01516.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*282C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 10/10 | 282 | chr8 | 66174875 | |||||
chr8:66175023
|
G | A | 1 | a0001c0001t0005 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 10/10 | 430 | chr8 | 66175023 | |||||
chr8:66175072
|
A | G | 1 | a0002c0002t0003 | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*479A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 10/10 | 479 | chr8 | 66175072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:66127672
|
C | CA | 12 | a0002c0003t0002g0004a0002c0003t0002g0005a0002c0003t0002g0006others(9): Show | 15 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+249dupA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 66127672 | |||||
chr8:66127704
|
G | C | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 10 | HG00140.hp1 HG00438.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+268G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66127704 | ||||||
chr8:66127882
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169-422A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66127882 | ||||||
chr8:66127895
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.169-409A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66127895 | ||||||
chr8:66128005
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.169-299A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66128005 | ||||||
chr8:66128231
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.169-73A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66128231 | ||||||
chr8:66128234
|
G | A | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.169-70G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 1/9 | chr8 | 66128234 | ||||||
chr8:66128561
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.341+85G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128561 | ||||||
chr8:66128562
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.341+86C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128562 | ||||||
chr8:66128844
|
GA | G | 18 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(15): Show | 21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.341+377delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66128844 | |||||
chr8:66128851
|
A | C | 8 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(5): Show | 9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.341+375A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128851 | ||||||
chr8:66128852
|
A | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01258.hp2 HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.341+376A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128852 | ||||||
chr8:66128897
|
C | T | 4 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0001g0053others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.341+421C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128897 | ||||||
chr8:66128950
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.341+474A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66128950 | ||||||
chr8:66129119
|
A | G | 1 | a0002c0004t0001g0223 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.341+643A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129119 | ||||||
chr8:66129150
|
A | G | 65 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(62): Show | 73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.341+674A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129150 | ||||||
chr8:66129345
|
G | A | 1 | a0001c0005t0001g0062 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.341+869G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129345 | ||||||
chr8:66129403
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.341+927T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129403 | ||||||
chr8:66129777
|
C | T | 1 | a0002c0008t0001g0050 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.341+1301C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129777 | ||||||
chr8:66129961
|
G | C | 2 | a0002c0003t0001g0033a0002c0003t0001g0034 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.341+1485G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66129961 | ||||||
chr8:66130278
|
C | T | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.341+1802C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130278 | ||||||
chr8:66130543
|
G | C | 2 | a0002c0002t0001g0040a0002c0008t0001g0050 | 2 | HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.341+2067G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130543 | ||||||
chr8:66130562
|
C | CG | 72 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(69): Show | 78 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.341+2094dupG | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130562 | |||||
chr8:66130659
|
C | CT | 22 | a0001c0001t0001g0215a0002c0002t0002g0059a0002c0002t0002g0060others(19): Show | 26 | HG00639.hp2 HG00673.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.341+2202dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130659 | |||||
chr8:66130659
|
CTT | C | 17 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(14): Show | 20 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.341+2201_341+2202d others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130659 | |||||
chr8:66130659
|
CTTT | C | 21 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(18): Show | 22 | HG00140.hp1 HG00438.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+2200_341+2202d others(5): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 66130659 | |||||
chr8:66130712
|
G | C | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+2236G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130712 | ||||||
chr8:66130761
|
C | T | 1 | a0002c0004t0001g0013 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.341+2285C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130761 | ||||||
chr8:66130795
|
G | A | 18 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(15): Show | 21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.341+2319G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130795 | ||||||
chr8:66130883
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18612.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.341+2407G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130883 | ||||||
chr8:66130888
|
C | T | 25 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(22): Show | 29 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.341+2412C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66130888 | ||||||
chr8:66131109
|
A | G | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+2633A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131109 | ||||||
chr8:66131282
|
G | A | 65 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(62): Show | 73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.341+2806G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131282 | ||||||
chr8:66131293
|
G | A | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+2817G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131293 | ||||||
chr8:66131386
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.341+2910G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131386 | ||||||
chr8:66131808
|
T | C | 64 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(61): Show | 72 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.342-3182T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131808 | ||||||
chr8:66131922
|
C | G | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.342-3068C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66131922 | ||||||
chr8:66132268
|
T | C | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-2722T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132268 | ||||||
chr8:66132344
|
T | A | 6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-2646T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132344 | ||||||
chr8:66132544
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG03516.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342-2446G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132544 | ||||||
chr8:66132558
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.342-2432C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132558 | ||||||
chr8:66132592
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.342-2398C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132592 | ||||||
chr8:66132660
|
G | C | 19 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 20 | HG00140.hp1 HG00438.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.342-2330G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132660 | ||||||
chr8:66132804
|
CCTAAA | C | 20 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(17): Show | 24 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-2185_342-2181d others(7): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132804 | ||||||
chr8:66132841
|
T | C | 65 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(62): Show | 73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.342-2149T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132841 | ||||||
chr8:66132924
|
T | A | 1 | a0002c0004t0001g0013 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.342-2066T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132924 | ||||||
chr8:66132971
|
C | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG00140.hp1 HG00438.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-2019C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66132971 | ||||||
chr8:66133039
|
G | C | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(5): Show | 8 | HG00639.hp1 HG00735.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.342-1951G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133039 | ||||||
chr8:66133070
|
C | T | 1 | a0004c0007t0001g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.342-1920C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133070 | ||||||
chr8:66133364
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0224 | 3 | HG01123.hp2 HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.342-1626T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133364 | ||||||
chr8:66133474
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.342-1516G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133474 | ||||||
chr8:66133501
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.342-1489G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133501 | ||||||
chr8:66133550
|
A | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG03516.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342-1440A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133550 | ||||||
chr8:66133618
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.342-1372A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133618 | ||||||
chr8:66133639
|
G | A | 65 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(62): Show | 73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.342-1351G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133639 | ||||||
chr8:66133685
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.342-1305A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133685 | ||||||
chr8:66133702
|
G | T | 18 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(15): Show | 21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-1288G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133702 | ||||||
chr8:66133743
|
A | C | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.342-1247A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133743 | ||||||
chr8:66133795
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.342-1195A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133795 | ||||||
chr8:66133948
|
C | T | 4 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-1042C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133948 | ||||||
chr8:66133951
|
A | T | 18 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(15): Show | 21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-1039A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66133951 | ||||||
chr8:66134081
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0213 | 2 | HG02027.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.342-909A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134081 | ||||||
chr8:66134124
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.342-866A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134124 | ||||||
chr8:66134349
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.342-641G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134349 | ||||||
chr8:66134480
|
C | T | 52 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(49): Show | 59 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.342-510C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134480 | ||||||
chr8:66134747
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 53 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.342-243C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134747 | ||||||
chr8:66134959
|
G | T | 1 | a0002c0002t0002g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.342-31G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 2/9 | chr8 | 66134959 | ||||||
chr8:66135243
|
G | A | 1 | a0002c0003t0002g0005 | 2 | HG00639.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.507+88G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135243 | ||||||
chr8:66135314
|
T | C | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.507+159T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135314 | ||||||
chr8:66135348
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.507+193C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135348 | ||||||
chr8:66135418
|
C | T | 1 | a0002c0002t0001g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.507+263C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135418 | ||||||
chr8:66135578
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.507+423T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135578 | ||||||
chr8:66135588
|
C | A | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.507+433C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135588 | ||||||
chr8:66135718
|
A | C | 4 | a0002c0003t0002g0008a0002c0003t0002g0056a0002c0003t0002g0057others(1): Show | 5 | HG02723.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+563A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135718 | ||||||
chr8:66135746
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG01243.hp2 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.507+591C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135746 | ||||||
chr8:66135929
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG02027.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.507+774A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66135929 | ||||||
chr8:66136405
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.508-690T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66136405 | ||||||
chr8:66136730
|
T | C | 1 | a0002c0003t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.508-365T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66136730 | ||||||
chr8:66136753
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.508-342A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66136753 | ||||||
chr8:66137020
|
A | T | 14 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(11): Show | 15 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.508-75A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66137020 | ||||||
chr8:66137043
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.508-52G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66137043 | ||||||
chr8:66137063
|
A | C | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-32A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 3/9 | chr8 | 66137063 | ||||||
chr8:66137383
|
G | A | 13 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(10): Show | 16 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.603+193G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137383 | ||||||
chr8:66137758
|
G | GA | 15 | a0001c0001t0001g0063a0001c0001t0001g0108a0001c0001t0001g0109others(12): Show | 16 | HG01109.hp2 HG01243.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.603+588dupA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | |||||
chr8:66137758
|
G | GAA | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG02451.hp2 HG02717.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.603+587_603+588dup others(2): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | |||||
chr8:66137758
|
GA | G | 74 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0026others(71): Show | 77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.603+588delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | |||||
chr8:66137758
|
GAA | G | 15 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0209others(12): Show | 16 | HG01167.hp1 HG02083.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.603+587_603+588del others(2): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66137758 | |||||
chr8:66137781
|
T | A | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.603+591T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137781 | ||||||
chr8:66137823
|
T | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+633T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137823 | ||||||
chr8:66137964
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.603+774A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66137964 | ||||||
chr8:66138039
|
T | G | 20 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(17): Show | 24 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.603+849T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138039 | ||||||
chr8:66138061
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.603+871A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138061 | ||||||
chr8:66138330
|
C | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 120 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.603+1140C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138330 | ||||||
chr8:66138413
|
G | A | 1 | a0002c0003t0001g0037 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.603+1223G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138413 | ||||||
chr8:66138532
|
G | A | 14 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(11): Show | 15 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.603+1342G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138532 | ||||||
chr8:66138784
|
T | A | 66 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0027others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.603+1594T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138784 | ||||||
chr8:66138825
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.603+1635T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138825 | ||||||
chr8:66138952
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.603+1762C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138952 | ||||||
chr8:66138998
|
G | A | 10 | a0001c0001t0001g0146a0002c0004t0001g0013a0002c0004t0001g0216others(7): Show | 11 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.603+1808G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66138998 | ||||||
chr8:66139246
|
C | T | 4 | a0002c0003t0002g0008a0002c0003t0002g0056a0002c0003t0002g0057others(1): Show | 5 | HG02723.hp2 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+2056C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139246 | ||||||
chr8:66139275
|
G | A | 1 | a0002c0003t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.603+2085G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139275 | ||||||
chr8:66139280
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.603+2090T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139280 | ||||||
chr8:66139476
|
TC | T | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.603+2287delC | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139476 | ||||||
chr8:66139477
|
CA | C | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+2288delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139477 | ||||||
chr8:66139478
|
A | T | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.603+2288A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139478 | ||||||
chr8:66139580
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.603+2390C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139580 | ||||||
chr8:66139876
|
C | T | 60 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(57): Show | 68 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.603+2686C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66139876 | ||||||
chr8:66140055
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01109.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.603+2865G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140055 | ||||||
chr8:66140081
|
A | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0027others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.603+2891A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140081 | ||||||
chr8:66140160
|
A | G | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.603+2970A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140160 | ||||||
chr8:66140334
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(190): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.603+3144G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140334 | ||||||
chr8:66140472
|
T | G | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+3282T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140472 | ||||||
chr8:66140509
|
C | T | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 52 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.603+3319C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140509 | ||||||
chr8:66140777
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.603+3587G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140777 | ||||||
chr8:66140787
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0010t0001g0153 | 3 | HG00741.hp1 HG02280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.603+3597G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140787 | ||||||
chr8:66140913
|
A | G | 1 | a0002c0004t0001g0223 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.603+3723A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140913 | ||||||
chr8:66140966
|
A | G | 25 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(22): Show | 29 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.603+3776A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66140966 | ||||||
chr8:66141007
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.603+3817C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141007 | ||||||
chr8:66141206
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.603+4016A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141206 | ||||||
chr8:66141329
|
C | T | 2 | a0002c0004t0001g0221a0002c0004t0001g0223 | 2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.603+4139C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141329 | ||||||
chr8:66141339
|
G | A | 3 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0232 | 3 | HG02486.hp1 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.603+4149G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141339 | ||||||
chr8:66141349
|
G | T | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.603+4159G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141349 | ||||||
chr8:66141474
|
G | A | 1 | a0002c0002t0001g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.603+4284G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141474 | ||||||
chr8:66141483
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.603+4293G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141483 | ||||||
chr8:66141545
|
C | G | 1 | a0001c0011t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.603+4355C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141545 | ||||||
chr8:66141924
|
G | A | 60 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(57): Show | 68 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.603+4734G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141924 | ||||||
chr8:66141947
|
T | A | 1 | a0001c0005t0001g0072 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.603+4757T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141947 | ||||||
chr8:66141993
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG00735.hp1 HG01361.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.603+4803T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66141993 | ||||||
chr8:66142023
|
G | A | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.603+4833G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142023 | ||||||
chr8:66142100
|
C | A | 2 | a0002c0003t0002g0006a0002c0003t0002g0021 | 3 | HG01175.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.603+4910C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142100 | ||||||
chr8:66142326
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.603+5136G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142326 | ||||||
chr8:66142435
|
G | A | 8 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(5): Show | 9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.603+5245G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66142435 | ||||||
chr8:66143003
|
TG | T | 18 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(15): Show | 21 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.603+5815delG | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66143003 | |||||
chr8:66143295
|
G | A | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.603+6105G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143295 | ||||||
chr8:66143582
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.604-6063G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143582 | ||||||
chr8:66143584
|
T | A | 14 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(11): Show | 15 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.604-6061T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143584 | ||||||
chr8:66143630
|
T | G | 6 | a0002c0004t0001g0217a0002c0004t0001g0218a0002c0004t0001g0219others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.604-6015T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143630 | ||||||
chr8:66143738
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.604-5907T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143738 | ||||||
chr8:66143781
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.604-5864A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143781 | ||||||
chr8:66143794
|
C | A | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-5851C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143794 | ||||||
chr8:66143800
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.604-5845A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143800 | ||||||
chr8:66143891
|
G | A | 8 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(5): Show | 9 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.604-5754G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66143891 | ||||||
chr8:66144166
|
G | T | 1 | a0001c0005t0001g0170 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.604-5479G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144166 | ||||||
chr8:66144311
|
T | G | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.604-5334T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144311 | ||||||
chr8:66144412
|
T | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | HG03017.hp2 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.604-5233T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144412 | ||||||
chr8:66144505
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.604-5140G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144505 | ||||||
chr8:66144611
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.604-5034A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144611 | ||||||
chr8:66144700
|
G | C | 44 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(41): Show | 51 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.604-4945G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144700 | ||||||
chr8:66144909
|
T | A | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.604-4736T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144909 | ||||||
chr8:66144979
|
G | A | 1 | a0002c0002t0002g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.604-4666G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66144979 | ||||||
chr8:66145025
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.604-4620A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145025 | ||||||
chr8:66145035
|
T | C | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604-4610T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145035 | ||||||
chr8:66145575
|
G | A | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.604-4070G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145575 | ||||||
chr8:66145635
|
C | T | 16 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(13): Show | 17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.604-4010C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145635 | ||||||
chr8:66145639
|
A | G | 27 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0027others(24): Show | 28 | HG00140.hp1 HG00438.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.604-4006A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145639 | ||||||
chr8:66145660
|
G | GT | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-3975dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66145660 | |||||
chr8:66145714
|
G | A | 1 | a0002c0002t0001g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.604-3931G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145714 | ||||||
chr8:66145722
|
G | A | 10 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0041others(7): Show | 13 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.604-3923G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145722 | ||||||
chr8:66145986
|
G | A | 21 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035others(18): Show | 25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.604-3659G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66145986 | ||||||
chr8:66146101
|
G | A | 2 | a0002c0006t0001g0119a0002c0006t0001g0151 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.604-3544G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66146101 | ||||||
chr8:66146208
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.604-3437G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66146208 | ||||||
chr8:66146315
|
CT | C | 22 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(19): Show | 25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.604-3328delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66146315 | |||||
chr8:66146740
|
T | C | 16 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(13): Show | 17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.604-2905T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66146740 | ||||||
chr8:66147018
|
A | G | 43 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(40): Show | 50 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.604-2627A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147018 | ||||||
chr8:66147234
|
T | C | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.604-2411T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147234 | ||||||
chr8:66147322
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0010t0001g0153 | 3 | HG00741.hp1 HG02280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.604-2323T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147322 | ||||||
chr8:66147534
|
C | T | 16 | a0002c0003t0002g0004a0002c0003t0002g0005a0002c0003t0002g0006others(13): Show | 20 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.604-2111C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147534 | ||||||
chr8:66147562
|
C | T | 21 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035others(18): Show | 25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.604-2083C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147562 | ||||||
chr8:66147651
|
C | T | 11 | a0001c0001t0001g0071a0001c0001t0001g0135a0001c0001t0001g0140others(8): Show | 11 | HG00621.hp2 HG00673.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.604-1994C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147651 | ||||||
chr8:66147688
|
A | G | 2 | a0002c0006t0001g0119a0002c0006t0001g0151 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.604-1957A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147688 | ||||||
chr8:66147699
|
G | A | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.604-1946G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147699 | ||||||
chr8:66147794
|
C | CA | 16 | a0001c0001t0001g0026a0001c0001t0001g0074a0001c0001t0001g0075others(13): Show | 16 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.604-1828dupA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147794 | |||||
chr8:66147794
|
CA | C | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(10): Show | 13 | HG00609.hp1 HG00741.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.604-1828delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147794 | |||||
chr8:66147811
|
A | AAC | 5 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0051others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-1833_604-1832i others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147811 | |||||
chr8:66147811
|
A | AC | 17 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(14): Show | 20 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.604-1834_604-1833i others(3): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147811 | ||||||
chr8:66147813
|
A | AAC | 20 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035others(17): Show | 24 | HG00639.hp2 HG02055.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.604-1831_604-1830i others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66147813 | |||||
chr8:66147813
|
A | C | 37 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(34): Show | 40 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.604-1832A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147813 | ||||||
chr8:66147913
|
A | G | 1 | a0001c0005t0001g0062 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.604-1732A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66147913 | ||||||
chr8:66148226
|
ATAAT | A | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.604-1412_604-1409d others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr8 | 66148226 | |||||
chr8:66148286
|
A | C | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-1359A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148286 | ||||||
chr8:66148330
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.604-1315A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148330 | ||||||
chr8:66148386
|
T | C | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.604-1259T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148386 | ||||||
chr8:66148863
|
A | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG00140.hp1 HG01258.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.604-782A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66148863 | ||||||
chr8:66149012
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.604-633G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66149012 | ||||||
chr8:66149253
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.604-392A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66149253 | ||||||
chr8:66149402
|
A | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.604-243A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 4/9 | chr8 | 66149402 | ||||||
chr8:66149970
|
T | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+92T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/9 | chr8 | 66149970 | ||||||
chr8:66150059
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.838-158G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/9 | chr8 | 66150059 | ||||||
chr8:66150134
|
G | T | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.838-83G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 5/9 | chr8 | 66150134 | ||||||
chr8:66150637
|
G | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.985+171G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150637 | ||||||
chr8:66150673
|
C | CT | 18 | a0001c0001t0001g0066a0001c0001t0001g0098a0001c0001t0001g0099others(15): Show | 18 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.985+220dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66150673 | |||||
chr8:66150674
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.985+208T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150674 | ||||||
chr8:66150807
|
C | G | 16 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(13): Show | 17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.985+341C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150807 | ||||||
chr8:66150828
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | NA18942.hp1 NA18946.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.985+362G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66150828 | ||||||
chr8:66151057
|
T | C | 2 | a0002c0006t0001g0119a0002c0006t0001g0151 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.985+591T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151057 | ||||||
chr8:66151143
|
T | A | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.985+677T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151143 | ||||||
chr8:66151182
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.985+716G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151182 | ||||||
chr8:66151294
|
A | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.985+828A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151294 | ||||||
chr8:66151432
|
C | G | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.986-945C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151432 | ||||||
chr8:66151570
|
A | T | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-807A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151570 | ||||||
chr8:66151666
|
A | G | 16 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(13): Show | 19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.986-711A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151666 | ||||||
chr8:66151846
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.986-531A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151846 | ||||||
chr8:66151849
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.986-528A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151849 | ||||||
chr8:66151850
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.986-527T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151850 | ||||||
chr8:66151850
|
T | TAATA | 6 | a0001c0001t0001g0101a0001c0001t0001g0135a0001c0001t0001g0150others(3): Show | 6 | HG01516.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.986-484_986-481dup others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | |||||
chr8:66151850
|
TAATA | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 78 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.986-484_986-481del others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | |||||
chr8:66151850
|
TAATAAAT others(1): Show |
T | 18 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(15): Show | 18 | HG00140.hp1 HG00735.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.986-488_986-481del others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | |||||
chr8:66151850
|
TAATAAAT others(5): Show |
T | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG02015.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.986-492_986-481del others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | |||||
chr8:66151850
|
TAATAAAT others(9): Show |
T | 3 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025 | 3 | HG02809.hp2 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.986-496_986-481del others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66151850 | |||||
chr8:66151963
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.986-414G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66151963 | ||||||
chr8:66152163
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.986-214A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | chr8 | 66152163 | ||||||
chr8:66152288
|
CT | C | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.986-87delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 66152288 | |||||
chr8:66152756
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1236+129G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66152756 | ||||||
chr8:66152801
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1236+174G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66152801 | ||||||
chr8:66152903
|
T | TTG | 30 | a0001c0001t0001g0002a0001c0001t0001g0073a0001c0001t0001g0074others(27): Show | 32 | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1236+318_1236+319d others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
T | TTGTG | 19 | a0001c0001t0001g0009a0001c0001t0001g0076a0001c0001t0001g0089others(16): Show | 20 | HG01167.hp2 HG01243.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1236+316_1236+319d others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
T | TTGTGTG | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0110others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+314_1236+319d others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0066a0001c0005t0001g0072a0002c0002t0003g0032 | 3 | HG02145.hp2 HG06807.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1236+312_1236+319d others(10): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
TTG | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0026others(46): Show | 55 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1236+318_1236+319d others(4): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
TTGTG | T | 17 | a0001c0001t0001g0085a0001c0001t0001g0113a0001c0001t0001g0125others(14): Show | 18 | HG00544.hp2 HG00639.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1236+316_1236+319d others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
TTGTGTG | T | 19 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0051others(16): Show | 22 | HG01175.hp1 HG02004.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1236+314_1236+319d others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
TTGTGTGT others(3): Show |
T | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1236+310_1236+319d others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0005g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1236+308_1236+319d others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152903
|
TTGTGTGT others(13): Show |
T | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1236+300_1236+319d others(22): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66152903 | |||||
chr8:66152942
|
T | A | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1236+315T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66152942 | ||||||
chr8:66153040
|
G | A | 1 | a0002c0003t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1236+413G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153040 | ||||||
chr8:66153061
|
C | T | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1236+434C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153061 | ||||||
chr8:66153065
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1236+438G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153065 | ||||||
chr8:66153207
|
C | T | 1 | a0002c0004t0001g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1236+580C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153207 | ||||||
chr8:66153237
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0171a0001c0001t0001g0174 | 3 | HG01109.hp2 HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1236+610A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153237 | ||||||
chr8:66153339
|
C | T | 1 | a0001c0001t0005g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1237-708C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153339 | ||||||
chr8:66153539
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1237-508G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153539 | ||||||
chr8:66153570
|
G | C | 1 | a0002c0002t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1237-477G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153570 | ||||||
chr8:66153635
|
G | A | 1 | a0002c0002t0001g0046 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1237-412G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153635 | ||||||
chr8:66153649
|
AT | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 45 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1237-397delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153649 | ||||||
chr8:66153737
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0203 | 2 | NA18980.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1237-310T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153737 | ||||||
chr8:66153859
|
A | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01109.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1237-188A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66153859 | ||||||
chr8:66154003
|
CT | C | 41 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0087others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.1237-33delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 66154003 | |||||
chr8:66154006
|
T | C | 7 | a0002c0002t0001g0231a0002c0003t0002g0004a0002c0003t0002g0005others(4): Show | 10 | HG00639.hp2 HG01175.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237-41T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 8/9 | chr8 | 66154006 | ||||||
chr8:66154349
|
A | G | 1 | a0002c0004t0001g0216 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1524+15A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154349 | ||||||
chr8:66154387
|
C | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+53C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154387 | ||||||
chr8:66154468
|
A | G | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+134A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154468 | ||||||
chr8:66154545
|
C | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+211C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66154545 | ||||||
chr8:66155113
|
G | A | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+779G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155113 | ||||||
chr8:66155254
|
A | G | 1 | a0002c0004t0001g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1524+920A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155254 | ||||||
chr8:66155389
|
G | A | 1 | a0002c0002t0001g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1524+1055G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155389 | ||||||
chr8:66155460
|
G | A | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+1126G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155460 | ||||||
chr8:66155896
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(225): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1524+1562T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155896 | ||||||
chr8:66155921
|
A | G | 1 | a0002c0002t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1524+1587A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155921 | ||||||
chr8:66155998
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1524+1664C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66155998 | ||||||
chr8:66156340
|
A | C | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2006A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156340 | ||||||
chr8:66156421
|
G | A | 2 | a0002c0006t0001g0119a0002c0006t0001g0151 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1524+2087G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156421 | ||||||
chr8:66156427
|
T | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+2093T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156427 | ||||||
chr8:66156439
|
C | T | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+2105C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156439 | ||||||
chr8:66156670
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1524+2336C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156670 | ||||||
chr8:66156687
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1524+2353C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156687 | ||||||
chr8:66156868
|
A | G | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+2534A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66156868 | ||||||
chr8:66157000
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0089a0001c0001t0001g0095others(1): Show | 5 | HG02015.hp2 HG02071.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+2666C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157000 | ||||||
chr8:66157097
|
A | C | 1 | a0002c0002t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1524+2763A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157097 | ||||||
chr8:66157153
|
T | C | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+2819T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157153 | ||||||
chr8:66157294
|
A | G | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+2960A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157294 | ||||||
chr8:66157390
|
A | C | 1 | a0002c0002t0003g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1524+3056A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157390 | ||||||
chr8:66157505
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1524+3171G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157505 | ||||||
chr8:66157538
|
G | A | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+3204G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157538 | ||||||
chr8:66157599
|
G | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3265G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157599 | ||||||
chr8:66157662
|
T | C | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+3328T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157662 | ||||||
chr8:66157743
|
C | T | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+3409C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157743 | ||||||
chr8:66157902
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3568G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157902 | ||||||
chr8:66157920
|
C | T | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1524+3586C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157920 | ||||||
chr8:66157956
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1524+3622C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66157956 | ||||||
chr8:66158065
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1524+3731G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158065 | ||||||
chr8:66158135
|
TCCCCACC others(6): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1524+3802_1524+381 others(17): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158135 | ||||||
chr8:66158136
|
C | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0116a0001c0001t0001g0130 | 3 | HG02300.hp2 NA18998.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1524+3802C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158136 | ||||||
chr8:66158137
|
C | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0193a0001c0005t0001g0166 | 3 | HG01261.hp1 NA19066.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1524+3803C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158137 | ||||||
chr8:66158137
|
CCCACCAC others(3): Show |
C | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1524+3805_1524+381 others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158137 | |||||
chr8:66158137
|
CCCACCAC others(5): Show |
C | 1 | a0001c0001t0001g0205 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1524+3805_1524+381 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158137 | |||||
chr8:66158138
|
CCACCACA others(4): Show |
C | 2 | a0001c0001t0001g0114a0001c0001t0001g0167 | 2 | NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1524+3808_1524+381 others(15): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158138 | |||||
chr8:66158138
|
CCACCACA others(16): Show |
C | 1 | a0001c0001t0001g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1524+3808_1524+383 others(27): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158138 | |||||
chr8:66158140
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1524+3806A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158140 | ||||||
chr8:66158141
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1524+3807C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158141 | ||||||
chr8:66158141
|
C | CCA | 17 | a0001c0001t0001g0073a0001c0001t0001g0086a0001c0001t0001g0091others(14): Show | 17 | HG00738.hp1 HG00741.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.1524+3867_1524+386 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
C | CCACA | 11 | a0001c0001t0001g0065a0001c0001t0001g0085a0001c0001t0001g0098others(8): Show | 11 | HG02970.hp1 HG03195.hp2 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+3865_1524+386 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCA | C | 31 | a0001c0001t0001g0009a0001c0001t0001g0071a0001c0001t0001g0074others(28): Show | 35 | HG00099.hp1 HG00673.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1524+3867_1524+386 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACA | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0067a0001c0001t0001g0068others(24): Show | 30 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1524+3865_1524+386 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACA | C | 29 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0027others(26): Show | 30 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1524+3863_1524+386 others(10): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(1): Show |
C | 24 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0121others(21): Show | 25 | HG00280.hp1 HG00438.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1524+3861_1524+386 others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(3): Show |
C | 14 | a0001c0001t0001g0029a0001c0001t0001g0083a0001c0001t0001g0094others(11): Show | 14 | HG00621.hp1 HG01175.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1524+3859_1524+386 others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(5): Show |
C | 5 | a0001c0001t0001g0063a0001c0001t0001g0175a0002c0003t0001g0036others(2): Show | 5 | HG01433.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3857_1524+386 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(7): Show |
C | 5 | a0002c0003t0002g0008a0002c0003t0002g0056a0002c0003t0002g0057others(2): Show | 6 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+3855_1524+386 others(18): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(9): Show |
C | 4 | a0001c0001t0001g0100a0001c0001t0001g0142a0002c0003t0002g0058others(1): Show | 5 | HG02630.hp1 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3853_1524+386 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(11): Show |
C | 1 | a0002c0004t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1524+3851_1524+386 others(22): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(13): Show |
C | 2 | a0002c0002t0001g0045a0002c0002t0003g0024 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1524+3849_1524+386 others(24): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(15): Show |
C | 5 | a0002c0002t0003g0023a0002c0002t0003g0025a0002c0002t0003g0032others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3847_1524+386 others(26): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(17): Show |
C | 6 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0147others(3): Show | 8 | HG00673.hp1 HG01123.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+3845_1524+386 others(28): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158141
|
CCACACAC others(23): Show |
C | 5 | a0002c0002t0001g0049a0002c0002t0001g0051a0002c0002t0001g0052others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3839_1524+386 others(34): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66158141 | |||||
chr8:66158385
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1524+4051T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158385 | ||||||
chr8:66158386
|
C | A | 22 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(19): Show | 25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1524+4052C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158386 | ||||||
chr8:66158897
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1524+4563T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66158897 | ||||||
chr8:66159183
|
C | T | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+4849C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159183 | ||||||
chr8:66159225
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1524+4891A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159225 | ||||||
chr8:66159241
|
T | C | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+4907T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159241 | ||||||
chr8:66159265
|
G | A | 16 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(13): Show | 17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+4931G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159265 | ||||||
chr8:66159411
|
A | G | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+5077A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159411 | ||||||
chr8:66159486
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+5152G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159486 | ||||||
chr8:66159699
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG00140.hp1 HG01258.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1524+5365T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159699 | ||||||
chr8:66159703
|
A | G | 1 | a0001c0005t0001g0062 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1524+5369A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159703 | ||||||
chr8:66159929
|
C | A | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+5595C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159929 | ||||||
chr8:66159984
|
T | C | 11 | a0001c0001t0001g0112a0001c0001t0001g0136a0001c0001t0001g0184others(8): Show | 11 | HG00741.hp2 HG01192.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+5650T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66159984 | ||||||
chr8:66160102
|
A | C | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1524+5768A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160102 | ||||||
chr8:66160191
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+5857A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160191 | ||||||
chr8:66160227
|
A | G | 5 | a0002c0002t0001g0049a0002c0002t0001g0051a0002c0002t0001g0052others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+5893A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160227 | ||||||
chr8:66160356
|
G | GGT | 14 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0108others(11): Show | 15 | HG00738.hp2 HG01070.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1524+6051_1524+605 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160356
|
G | GGTGT | 19 | a0001c0001t0001g0102a0001c0001t0001g0183a0001c0005t0001g0159others(16): Show | 20 | HG01167.hp2 HG01891.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524+6049_1524+605 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160356
|
G | GGTGTGT | 13 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(10): Show | 16 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1524+6047_1524+605 others(10): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160356
|
G | GGTGTGTG others(3): Show |
4 | a0002c0003t0001g0035a0002c0003t0002g0056a0002c0006t0001g0119others(1): Show | 4 | HG02559.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+6043_1524+605 others(14): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160356
|
G | GGTGTGTG others(5): Show |
12 | a0002c0003t0001g0036a0002c0003t0002g0004a0002c0003t0002g0005others(9): Show | 15 | HG00639.hp2 HG01175.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1524+6041_1524+605 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160356
|
G | GGTGTGTG others(7): Show |
4 | a0002c0003t0002g0008a0002c0003t0002g0017a0002c0003t0002g0020others(1): Show | 5 | HG02055.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+6039_1524+605 others(18): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160356
|
G | GGTGTGTG others(9): Show |
7 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0037others(4): Show | 7 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+6037_1524+605 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160356
|
G | GGTGTGTG others(11): Show |
2 | a0002c0004t0001g0219a0002c0004t0001g0221 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1524+6035_1524+605 others(22): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160356 | |||||
chr8:66160514
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+6180C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160514 | ||||||
chr8:66160564
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1524+6230G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160564 | ||||||
chr8:66160792
|
C | T | 16 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(13): Show | 17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+6458C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66160792 | ||||||
chr8:66160866
|
G | GTT | 12 | a0002c0002t0001g0031a0002c0004t0001g0013a0002c0004t0001g0216others(9): Show | 13 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1524+6544_1524+654 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160866 | |||||
chr8:66160866
|
GT | G | 5 | a0001c0001t0001g0089a0002c0002t0001g0051a0002c0002t0001g0052others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+6545delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66160866 | |||||
chr8:66161183
|
A | T | 1 | a0002c0002t0002g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1524+6849A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161183 | ||||||
chr8:66161461
|
A | T | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+7127A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161461 | ||||||
chr8:66161526
|
A | G | 2 | a0001c0001t0001g0136a0002c0002t0001g0049 | 2 | HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1524+7192A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161526 | ||||||
chr8:66161557
|
A | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+7223A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161557 | ||||||
chr8:66161635
|
C | T | 1 | a0002c0002t0001g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1524+7301C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161635 | ||||||
chr8:66161648
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1524+7314A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161648 | ||||||
chr8:66161694
|
CA | C | 16 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(13): Show | 17 | HG02145.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+7361delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161694 | ||||||
chr8:66161701
|
T | C | 2 | a0002c0003t0002g0014a0002c0003t0002g0020 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1524+7367T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161701 | ||||||
chr8:66161740
|
A | C | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1524+7406A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161740 | ||||||
chr8:66161755
|
G | GT | 143 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(140): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1524+7437dupT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | |||||
chr8:66161755
|
G | GTT | 37 | a0001c0001t0001g0065a0001c0001t0001g0102a0001c0005t0001g0159others(34): Show | 41 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1524+7436_1524+743 others(6): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | |||||
chr8:66161755
|
G | GTTT | 6 | a0002c0002t0001g0048a0002c0002t0001g0053a0002c0003t0001g0033others(3): Show | 6 | HG02572.hp1 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+7435_1524+743 others(7): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | |||||
chr8:66161755
|
GT | G | 5 | a0001c0001t0001g0173a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG00738.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+7437delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66161755 | |||||
chr8:66161776
|
G | C | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1524+7442G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161776 | ||||||
chr8:66161819
|
C | T | 1 | a0002c0002t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1524+7485C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161819 | ||||||
chr8:66161859
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1524+7525T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66161859 | ||||||
chr8:66162017
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | NA18942.hp1 NA18946.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1524+7683C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162017 | ||||||
chr8:66162102
|
CA | C | 16 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(13): Show | 19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1524+7769delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162102 | ||||||
chr8:66162159
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1524+7825G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162159 | ||||||
chr8:66162487
|
T | C | 1 | a0001c0001t0001g0003 | 3 | HG00673.hp1 HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1524+8153T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162487 | ||||||
chr8:66162599
|
A | G | 21 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035others(18): Show | 25 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1524+8265A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162599 | ||||||
chr8:66162905
|
A | T | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+8571A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162905 | ||||||
chr8:66162920
|
A | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1524+8586A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66162920 | ||||||
chr8:66163111
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1524+8777C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163111 | ||||||
chr8:66163310
|
T | C | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1524+8976T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163310 | ||||||
chr8:66163351
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1524+9017G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163351 | ||||||
chr8:66163556
|
C | T | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+9222C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163556 | ||||||
chr8:66163557
|
G | A | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | HG02486.hp1 HG03017.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+9223G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163557 | ||||||
chr8:66163906
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1524+9572A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163906 | ||||||
chr8:66163947
|
G | T | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1524+9613G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66163947 | ||||||
chr8:66164008
|
GT | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(45): Show | 52 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1524+9686delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164008 | |||||
chr8:66164358
|
G | A | 16 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(13): Show | 19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1524+10024G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164358 | ||||||
chr8:66164532
|
G | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00735.hp2 HG01516.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1525-9939G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164532 | ||||||
chr8:66164535
|
G | A | 1 | a0002c0003t0002g0021 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1525-9936G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164535 | ||||||
chr8:66164876
|
G | A | 2 | a0002c0006t0001g0119a0002c0006t0001g0151 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1525-9595G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164876 | ||||||
chr8:66164933
|
A | AGAAG | 9 | a0001c0001t0001g0098a0001c0001t0001g0125a0001c0001t0001g0150others(6): Show | 9 | HG00609.hp2 HG01109.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1525-9499_1525-949 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | |||||
chr8:66164933
|
A | G | 2 | a0001c0001t0001g0167a0001c0005t0001g0166 | 2 | NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1525-9538A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66164933 | ||||||
chr8:66164933
|
AGAAG | A | 55 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0027others(52): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.1525-9499_1525-949 others(8): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | |||||
chr8:66164933
|
AGAAGGAA others(1): Show |
A | 46 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(43): Show | 50 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1525-9503_1525-949 others(12): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | |||||
chr8:66164933
|
AGAAGGAA others(5): Show |
A | 8 | a0001c0001t0001g0104a0001c0001t0001g0142a0001c0001t0001g0203others(5): Show | 8 | HG02451.hp2 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-9507_1525-949 others(16): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | |||||
chr8:66164933
|
AGAAGGAA others(9): Show |
A | 56 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(53): Show | 64 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.1525-9511_1525-949 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | |||||
chr8:66164933
|
AGAAGGAA others(17): Show |
A | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-9519_1525-949 others(28): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66164933 | |||||
chr8:66165223
|
G | A | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1525-9248G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165223 | ||||||
chr8:66165268
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1525-9203G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165268 | ||||||
chr8:66165501
|
TATTTA | T | 4 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0036others(1): Show | 4 | HG02896.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-8965_1525-896 others(9): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66165501 | |||||
chr8:66165502
|
AT | A | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-8966delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66165502 | |||||
chr8:66165508
|
T | A | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-8963T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165508 | ||||||
chr8:66165760
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1525-8711A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165760 | ||||||
chr8:66165856
|
C | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-8615C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165856 | ||||||
chr8:66165924
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1525-8547C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66165924 | ||||||
chr8:66165952
|
CT | C | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-8508delT | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66165952 | |||||
chr8:66166045
|
TCTC | T | 11 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(8): Show | 12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1525-8422_1525-842 others(7): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66166045 | |||||
chr8:66166537
|
C | T | 1 | a0002c0003t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1525-7934C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66166537 | ||||||
chr8:66166556
|
G | A | 2 | a0002c0003t0002g0004a0002c0003t0002g0017 | 3 | HG02559.hp1 HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1525-7915G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66166556 | ||||||
chr8:66167031
|
A | G | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-7440A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167031 | ||||||
chr8:66167051
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1525-7420A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167051 | ||||||
chr8:66167533
|
A | G | 46 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(43): Show | 53 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1525-6938A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167533 | ||||||
chr8:66167870
|
C | G | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1525-6601C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167870 | ||||||
chr8:66167891
|
G | T | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1525-6580G>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167891 | ||||||
chr8:66167934
|
G | A | 16 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(13): Show | 19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1525-6537G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167934 | ||||||
chr8:66167950
|
A | G | 22 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(19): Show | 25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1525-6521A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66167950 | ||||||
chr8:66168408
|
C | T | 4 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0036others(1): Show | 4 | HG02896.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-6063C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168408 | ||||||
chr8:66168493
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1525-5978G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168493 | ||||||
chr8:66168807
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1525-5664G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168807 | ||||||
chr8:66168912
|
G | C | 5 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-5559G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66168912 | ||||||
chr8:66169147
|
C | A | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-5324C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169147 | ||||||
chr8:66169232
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1525-5239G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169232 | ||||||
chr8:66169290
|
C | T | 2 | a0002c0002t0001g0049a0002c0002t0001g0052 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1525-5181C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169290 | ||||||
chr8:66169475
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG03516.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1525-4996T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169475 | ||||||
chr8:66169504
|
C | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | NA18942.hp1 NA18946.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1525-4967C>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169504 | ||||||
chr8:66169593
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1525-4878A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169593 | ||||||
chr8:66169646
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1525-4825C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169646 | ||||||
chr8:66169896
|
T | A | 50 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(47): Show | 57 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1525-4575T>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169896 | ||||||
chr8:66169897
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1525-4574A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66169897 | ||||||
chr8:66170016
|
A | G | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-4455A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170016 | ||||||
chr8:66170455
|
A | T | 2 | a0002c0003t0002g0014a0002c0003t0002g0020 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1525-4016A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170455 | ||||||
chr8:66170497
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(110): Show | 125 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.1525-3974T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170497 | ||||||
chr8:66170538
|
G | A | 1 | a0002c0004t0001g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1525-3933G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170538 | ||||||
chr8:66170563
|
A | G | 1 | a0002c0003t0002g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1525-3908A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170563 | ||||||
chr8:66170639
|
C | T | 4 | a0002c0002t0003g0023a0002c0002t0003g0024a0002c0002t0003g0025others(1): Show | 4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-3832C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170639 | ||||||
chr8:66170685
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1525-3786G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170685 | ||||||
chr8:66170760
|
A | G | 16 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(13): Show | 19 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1525-3711A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170760 | ||||||
chr8:66170893
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1525-3578A>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66170893 | ||||||
chr8:66171040
|
G | A | 4 | a0002c0002t0002g0055a0002c0002t0002g0059a0002c0002t0002g0060others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-3431G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171040 | ||||||
chr8:66171534
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1525-2937T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171534 | ||||||
chr8:66171793
|
G | A | 26 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(23): Show | 30 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1525-2678G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171793 | ||||||
chr8:66171889
|
C | T | 2 | a0002c0002t0003g0023a0002c0002t0003g0025 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1525-2582C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66171889 | ||||||
chr8:66171970
|
G | GGGGTC | 113 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(110): Show | 125 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.1525-2499_1525-249 others(9): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66171970 | |||||
chr8:66172009
|
G | A | 9 | a0002c0004t0001g0013a0002c0004t0001g0216a0002c0004t0001g0217others(6): Show | 10 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1525-2462G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172009 | ||||||
chr8:66172038
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1525-2433A>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172038 | ||||||
chr8:66172060
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0185a0001c0001t0001g0187 | 3 | HG01261.hp2 HG04228.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1525-2411G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172060 | ||||||
chr8:66172067
|
GGAAGGAA others(9): Show |
G | 26 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(23): Show | 30 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1525-2388_1525-237 others(20): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66172067 | |||||
chr8:66172096
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-2375G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172096 | ||||||
chr8:66172144
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 49 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1525-2327T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172144 | ||||||
chr8:66172170
|
G | A | 36 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(33): Show | 40 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1525-2301G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172170 | ||||||
chr8:66172423
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1525-2048C>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172423 | ||||||
chr8:66172845
|
G | A | 22 | a0002c0002t0001g0031a0002c0003t0001g0033a0002c0003t0001g0034others(19): Show | 26 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525-1626G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172845 | ||||||
chr8:66172934
|
T | G | 26 | a0002c0002t0001g0031a0002c0002t0003g0023a0002c0002t0003g0024others(23): Show | 30 | HG00639.hp2 HG01175.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1525-1537T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172934 | ||||||
chr8:66172972
|
T | C | 1 | a0002c0002t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-1499T>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66172972 | ||||||
chr8:66173032
|
C | T | 36 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0038others(33): Show | 40 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.1525-1439C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173032 | ||||||
chr8:66173067
|
T | G | 22 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0040others(19): Show | 25 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1525-1404T>G | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173067 | ||||||
chr8:66173601
|
C | T | 1 | a0002c0004t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-870C>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173601 | ||||||
chr8:66173615
|
G | C | 1 | a0002c0002t0002g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1525-856G>C | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173615 | ||||||
chr8:66173629
|
G | A | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-842G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66173629 | ||||||
chr8:66174115
|
G | A | 62 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0031others(59): Show | 70 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.1525-356G>A | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66174115 | ||||||
chr8:66174170
|
TA | T | 5 | a0002c0002t0001g0031a0002c0002t0001g0038a0002c0002t0001g0039others(2): Show | 5 | HG02486.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-287delA | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66174170 | |||||
chr8:66174256
|
A | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01109.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1525-215A>T | TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | chr8 | 66174256 | ||||||
chr8:66174349
|
TATTGTTA others(11): Show |
T | 1 | a0001c0001t0001g0131 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1525-110_1525-93de others(19): Show |
TRIM55 | ENSG00000147573.17 | transcript | ENST00000315962.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr8 | 66174349 |