geneid | 7706 |
---|---|
ensemblid | ENSG00000121060.19 |
hgncid | 12932 |
symbol | TRIM25 |
name | tripartite motif containing 25 |
refseq_nuc | NM_005082.5 |
refseq_prot | NP_005073.2 |
ensembl_nuc | ENST00000316881.9 |
ensembl_prot | ENSP00000323889.4 |
mane_status | MANE Select |
chr | chr17 |
start | 56887909 |
end | 56914049 |
strand | - |
ver | v1.2 |
region | chr17:56887909-56914049 |
region5000 | chr17:56882909-56919049 |
regionname0 | TRIM25_chr17_56887909_56914049 |
regionname5000 | TRIM25_chr17_56882909_56919049 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 630 | 263 | 68 | 45 | 101 | 13 | 36 | 68 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002 | 1/1 | 630 | 96 | 10 | 27 | 44 | 2 | 11 | 39 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003 | 0/0 | 630 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0004 | 0/0 | 630 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0005 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0006 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0007 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0008 | 0/0 | 630 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0009 | 0/0 | 630 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0010 | 0/0 | 630 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0011 | 0/0 | 73 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1893 | 259 | 66 | 44 | 100 | 13 | 36 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0002 | 1/1 | 1893 | 96 | 10 | 27 | 44 | 2 | 11 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0003 | 0/0 | 1893 | 11 | 11 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0004 | 0/0 | 1893 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0005 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0006 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0007 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0008 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0009 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0010 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0011 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0012 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0013 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0014 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0015 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
c0016 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3853 | 189 | 19 | 22 | 114 | 3 | 30 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0002 | 0/0 | 3852 | 73 | 24 | 17 | 21 | 4 | 7 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0003 | 0/1 | 3852 | 43 | 6 | 24 | 3 | 5 | 4 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0004 | 0/0 | 3853 | 13 | 6 | 4 | 1 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0005 | 0/0 | 3853 | 8 | 8 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0006 | 0/0 | 3852 | 5 | 3 | 1 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0007 | 0/0 | 3852 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0008 | 0/0 | 3853 | 4 | 1 | 0 | 0 | 3 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0009 | 0/0 | 3853 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0010 | 0/0 | 3852 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0011 | 0/0 | 3852 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0012 | 0/0 | 3853 | 3 | 1 | 1 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0013 | 0/0 | 3856 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0014 | 0/0 | 3852 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0015 | 0/0 | 3853 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0016 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0017 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0018 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0019 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0020 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0021 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0022 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0023 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0024 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0025 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0026 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0027 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0028 | 0/0 | 3852 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0029 | 0/0 | 3852 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0030 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0031 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0032 | 0/0 | 3852 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0033 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0034 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0035 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0036 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0037 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0038 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0039 | 0/0 | 3852 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0040 | 0/0 | 3852 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
t0041 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 36 | 2 | 4 | 19 | 1 | 10 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0002 | 0/1 | 15 | 1 | 12 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0003 | 0/0 | 13 | 2 | 7 | 1 | 0 | 3 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0004 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0005 | 0/0 | 12 | 1 | 3 | 8 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0006 | 0/0 | 12 | 1 | 2 | 6 | 0 | 3 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0007 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0008 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1893 | 259 | 66 | 44 | 100 | 13 | 36 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0008 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0011 | 0/0 | 1893 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0012 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0014 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002 | 1/1 | 1893 | 96 | 10 | 27 | 44 | 2 | 11 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003 | 0/0 | 1893 | 11 | 11 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0007 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0004c0004 | 0/0 | 1893 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0005c0006 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0006c0015 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0007c0009 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0008c0013 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0009c0010 | 0/0 | 1893 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0010c0016 | 0/0 | 1893 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0011c0005 | 0/0 | 1893 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5745 | 146 | 16 | 18 | 84 | 3 | 25 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0002 | 0/0 | 5744 | 43 | 19 | 13 | 3 | 3 | 5 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0003 | 0/0 | 5744 | 23 | 5 | 11 | 3 | 4 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0004 | 0/0 | 5745 | 10 | 6 | 1 | 1 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0005 | 0/0 | 5745 | 8 | 8 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0006 | 0/0 | 5744 | 3 | 2 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0008 | 0/0 | 5745 | 4 | 1 | 0 | 0 | 3 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0009 | 0/0 | 5745 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0011 | 0/0 | 5744 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0012 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0015 | 0/0 | 5745 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0023 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0024 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0026 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0027 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0029 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0030 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0032 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0034 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0035 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0037 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0038 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0039 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0001t0041 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0008t0006 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0011t0003 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0012t0013 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0001c0014t0025 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0001 | 1/0 | 5745 | 34 | 2 | 4 | 23 | 0 | 4 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0002 | 0/0 | 5744 | 29 | 4 | 4 | 18 | 1 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0003 | 0/1 | 5744 | 18 | 1 | 12 | 0 | 0 | 4 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0004 | 0/0 | 5745 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0006 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0011 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0012 | 0/0 | 5745 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0014 | 0/0 | 5744 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0022 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0028 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0031 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0033 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0036 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0002c0002t0040 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003t0007 | 0/0 | 5744 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003t0010 | 0/0 | 5744 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003t0017 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003t0018 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003t0019 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003t0020 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0003t0021 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0003c0007t0016 | 0/0 | 5749 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0004c0004t0001 | 0/0 | 5745 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0005c0006t0007 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0006c0015t0002 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0007c0009t0001 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0008c0013t0003 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0009c0010t0013 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0010c0016t0001 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
a0011c0005t0001 | 0/0 | 5745 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | copy fasta | chr17 | 56882909 | 56919049 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 36 | 2 | 4 | 19 | 1 | 10 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0006 | 0/0 | 12 | 1 | 2 | 6 | 0 | 3 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0003 | 0/0 | 13 | 2 | 7 | 1 | 0 | 3 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0005g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0009g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0015g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0023g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0024g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0026g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0027g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0029g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0030g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0032g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0034g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0035g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0037g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0038g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0039g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0001t0041g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0008t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0011t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0012t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0001c0014t0025g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0004 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0008 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0005 | 0/0 | 12 | 1 | 3 | 8 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0003g0002 | 0/1 | 15 | 1 | 12 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0004g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0012g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0014g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0022g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0028g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0031g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0033g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0036g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0002c0002t0040g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0010g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0017g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0003t0021g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0003c0007t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0004c0004t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0004c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0004c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0005c0006t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0006c0015t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0007c0009t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0008c0013t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0009c0010t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0010c0016t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
a0011c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0158 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00099 | hp2 | a0002 | c0002 | t0028 | g0183 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00140 | hp2 | a0008 | c0013 | t0003 | g0130 | EUR | GBR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00438 | hp2 | a0001 | c0001 | t0034 | g0129 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00558 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00639 | hp1 | a0002 | c0002 | t0004 | g0067 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00639 | hp2 | a0002 | c0002 | t0004 | g0043 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00673 | hp2 | a0001 | c0001 | t0015 | g0033 | EAS | CHS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00735 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01069 | hp1 | a0002 | c0002 | t0006 | g0066 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01168 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01169 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01192 | hp2 | a0002 | c0002 | t0004 | g0043 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01255 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01256 | hp1 | a0001 | c0011 | t0003 | g0192 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01256 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01257 | hp2 | a0002 | c0002 | t0014 | g0024 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01258 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01358 | hp2 | a0002 | c0002 | t0012 | g0064 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01361 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01496 | hp1 | a0001 | c0001 | t0029 | g0162 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01496 | hp2 | a0002 | c0002 | t0014 | g0024 | AMR | CLM | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0042 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01515 | hp2 | a0001 | c0001 | t0008 | g0212 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0025 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01516 | hp2 | a0001 | c0001 | t0008 | g0128 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0042 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0121 | EUR | IBS | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01891 | hp2 | a0001 | c0001 | t0024 | g0086 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01978 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01993 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02040 | hp2 | a0002 | c0002 | t0036 | g0170 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02056 | hp2 | a0002 | c0002 | t0012 | g0168 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02071 | hp1 | a0001 | c0001 | t0038 | g0186 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02165 | hp1 | a0001 | c0001 | t0015 | g0033 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02257 | hp1 | a0003 | c0007 | t0016 | g0049 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02273 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02451 | hp2 | a0003 | c0003 | t0007 | g0021 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02622 | hp2 | a0002 | c0002 | t0031 | g0141 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02647 | hp2 | a0003 | c0003 | t0020 | g0054 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0127 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02698 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0100 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0085 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02895 | hp1 | a0003 | c0003 | t0010 | g0015 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02896 | hp1 | a0003 | c0003 | t0021 | g0055 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02922 | hp1 | a0003 | c0003 | t0007 | g0021 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02922 | hp2 | a0003 | c0003 | t0017 | g0052 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02976 | hp2 | a0001 | c0001 | t0037 | g0089 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03098 | hp1 | a0003 | c0003 | t0010 | g0015 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03130 | hp1 | a0003 | c0003 | t0019 | g0051 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03139 | hp1 | a0005 | c0006 | t0007 | g0056 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03195 | hp1 | a0002 | c0002 | t0022 | g0092 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03209 | hp1 | a0001 | c0001 | t0027 | g0109 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03225 | hp1 | a0009 | c0010 | t0013 | g0108 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03239 | hp1 | a0002 | c0002 | t0033 | g0166 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0084 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0111 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03654 | hp1 | a0001 | c0001 | t0039 | g0200 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03704 | hp2 | a0001 | c0001 | t0035 | g0201 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03831 | hp1 | a0001 | c0001 | t0032 | g0159 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03834 | hp1 | a0011 | c0005 | t0001 | g0057 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03927 | hp1 | a0002 | c0002 | t0003 | g0171 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03942 | hp2 | a0001 | c0001 | t0041 | g0102 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0174 | SAS | STU | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18522 | hp2 | a0002 | c0002 | t0011 | g0155 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18906 | hp1 | a0003 | c0003 | t0018 | g0050 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18946 | hp1 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18948 | hp1 | a0010 | c0016 | t0001 | g0217 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18951 | hp1 | a0004 | c0004 | t0001 | g0184 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18964 | hp2 | a0002 | c0002 | t0040 | g0180 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18971 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18972 | hp1 | a0004 | c0004 | t0001 | g0188 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18982 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19006 | hp2 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19009 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19030 | hp1 | a0003 | c0003 | t0010 | g0015 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19043 | hp1 | a0003 | c0003 | t0007 | g0053 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19043 | hp2 | a0006 | c0015 | t0002 | g0216 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19058 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19065 | hp1 | a0001 | c0014 | t0025 | g0088 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19085 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19091 | hp2 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA19240 | hp2 | a0001 | c0012 | t0013 | g0090 | AFR | YRI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | ASW | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | ASW | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0044 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0025 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0065 | SAS | GIH | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02486 | hp1 | a0001 | c0008 | t0006 | g0058 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0112 | AFR | ACB | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG03471 | hp2 | a0001 | c0001 | t0023 | g0207 | AFR | MSL | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG06807 | hp1 | a0001 | c0001 | t0026 | g0059 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
HG06807 | hp2 | a0001 | c0001 | t0030 | g0154 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
NA21309 | hp2 | a0007 | c0009 | t0001 | g0116 | AFR | LWK | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0002 | REF | REF | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0169 | REF | REF | TRIM25_chr17_56882909_56919049 | TRIM25 | chr17 | 56882909 | 56919049 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:56891791
|
T | C | 1 | a0009 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1802A>G | p.Tyr601Cys | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1863/5745 | 1802/1893 | 601/630 | chr17 | 56891791 | ||
chr17:56891819
|
C | T | 1 | a0008 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1774G>A | p.Ala592Thr | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1835/5745 | 1774/1893 | 592/630 | chr17 | 56891819 | ||
chr17:56901433
|
G | A | 7 | a0001a0003a0004others(4): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
missense_variant | MODERATE | c.1073C>T | p.Pro358Leu | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/9 | 1134/5745 | 1073/1893 | 358/630 | chr17 | 56901433 | ||
chr17:56904409
|
G | T | 1 | a0004 | 6 | NA18951.hp1 NA18972.hp1 NA18982.hp1 others(3): Show |
missense_variant | MODERATE | c.773C>A | p.Thr258Asn | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/9 | 834/5745 | 773/1893 | 258/630 | chr17 | 56904409 | ||
chr17:56904475
|
C | T | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.707G>A | p.Arg236Lys | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/9 | 768/5745 | 707/1893 | 236/630 | chr17 | 56904475 | ||
chr17:56913436
|
T | C | 3 | a0003a0005a0006 | 14 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(11): Show |
missense_variant | MODERATE | c.553A>G | p.Thr185Ala | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 614/5745 | 553/1893 | 185/630 | chr17 | 56913436 | ||
chr17:56913723
|
A | C | 2 | a0003a0005 | 13 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(10): Show |
missense_variant | MODERATE | c.266T>G | p.Val89Gly | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 327/5745 | 266/1893 | 89/630 | chr17 | 56913723 | ||
chr17:56913796
|
T | G | 1 | a0010 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.193A>C | p.Lys65Gln | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 254/5745 | 193/1893 | 65/630 | chr17 | 56913796 | ||
chr17:56913987
|
A | C | 1 | a0011 | 1 | HG03834.hp1 | start_lost | HIGH | c.2T>G | p.Met1? | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 63/5745 | 2/1893 | 1/630 | chr17 | 56913987 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:56891868
|
C | T | 2 | a0001c0012a0009c0010 | 2 | HG03225.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1725G>A | p.Thr575Thr | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1786/5745 | 1725/1893 | 575/630 | chr17 | 56891868 | ||
chr17:56891955
|
G | A | 1 | a0003c0007 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1638C>T | p.Ser546Ser | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1699/5745 | 1638/1893 | 546/630 | chr17 | 56891955 | ||
chr17:56899167
|
C | T | 1 | a0001c0011 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1101G>A | p.Glu367Glu | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/9 | 1162/5745 | 1101/1893 | 367/630 | chr17 | 56899167 | ||
chr17:56904402
|
T | C | 1 | a0001c0014 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.780A>G | p.Thr260Thr | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/9 | 841/5745 | 780/1893 | 260/630 | chr17 | 56904402 | ||
chr17:56908513
|
C | T | 1 | a0001c0008 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.648G>A | p.Ala216Ala | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/9 | 709/5745 | 648/1893 | 216/630 | chr17 | 56908513 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:56887993
|
T | C | 3 | a0001c0012t0013a0003c0007t0016a0009c0010t0013 | 3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3707A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3707 | chr17 | 56887993 | |||||
chr17:56888022
|
G | A | 2 | a0001c0001t0011a0002c0002t0011 | 3 | HG02486.hp2 HG02886.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3678C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3678 | chr17 | 56888022 | |||||
chr17:56888047
|
C | T | 1 | a0002c0002t0014 | 2 | HG01257.hp2 HG01496.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3653G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3653 | chr17 | 56888047 | |||||
chr17:56888115
|
T | C | 1 | a0001c0001t0035 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3585A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3585 | chr17 | 56888115 | |||||
chr17:56888174
|
G | A | 1 | a0002c0002t0036 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3526C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3526 | chr17 | 56888174 | |||||
chr17:56888498
|
CT | C | 31 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(28): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*3201delA | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3201 | chr17 | 56888498 | |||||
chr17:56888511
|
A | T | 1 | a0001c0001t0034 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3189T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3189 | chr17 | 56888511 | |||||
chr17:56888571
|
A | G | 6 | a0001c0001t0003a0001c0001t0024a0001c0011t0003others(3): Show | 46 | HG00140.hp2 HG00735.hp2 HG00741.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3129T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3129 | chr17 | 56888571 | |||||
chr17:56888584
|
C | T | 2 | a0001c0001t0030a0003c0003t0010 | 4 | HG02895.hp1 HG03098.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3116G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3116 | chr17 | 56888584 | |||||
chr17:56888606
|
G | T | 1 | a0002c0002t0033 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3094C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3094 | chr17 | 56888606 | |||||
chr17:56888672
|
G | A | 1 | a0002c0002t0031 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3028C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 3028 | chr17 | 56888672 | |||||
chr17:56888743
|
A | G | 1 | a0001c0001t0032 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2957 | chr17 | 56888743 | |||||
chr17:56888879
|
C | T | 1 | a0001c0001t0041 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2821G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2821 | chr17 | 56888879 | |||||
chr17:56888921
|
C | T | 1 | a0003c0003t0018 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2779G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2779 | chr17 | 56888921 | |||||
chr17:56889133
|
A | G | 3 | a0001c0012t0013a0003c0007t0016a0009c0010t0013 | 3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2567T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2567 | chr17 | 56889133 | |||||
chr17:56889176
|
T | TAAAA | 3 | a0001c0012t0013a0003c0007t0016a0009c0010t0013 | 3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2523_*2524insTTTT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2523 | chr17 | 56889176 | |||||
chr17:56889177
|
G | A | 3 | a0001c0012t0013a0003c0007t0016a0009c0010t0013 | 3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2523C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2523 | chr17 | 56889177 | |||||
chr17:56889183
|
T | A | 3 | a0001c0012t0013a0003c0007t0016a0009c0010t0013 | 3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2517A>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2517 | chr17 | 56889183 | |||||
chr17:56889223
|
C | T | 1 | a0003c0007t0016 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2477G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2477 | chr17 | 56889223 | |||||
chr17:56889224
|
G | A | 1 | a0001c0001t0032 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2476C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2476 | chr17 | 56889224 | |||||
chr17:56889329
|
T | G | 1 | a0001c0001t0009 | 4 | HG00558.hp1 NA18971.hp2 NA19006.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2371A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2371 | chr17 | 56889329 | |||||
chr17:56889339
|
C | A | 1 | a0001c0001t0015 | 2 | HG00673.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2361G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2361 | chr17 | 56889339 | |||||
chr17:56889444
|
A | G | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0026others(5): Show | 26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2256T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2256 | chr17 | 56889444 | |||||
chr17:56889576
|
G | A | 1 | a0001c0001t0037 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2124C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 2124 | chr17 | 56889576 | |||||
chr17:56889788
|
G | A | 1 | a0003c0003t0019 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1912C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1912 | chr17 | 56889788 | |||||
chr17:56889895
|
A | G | 1 | a0001c0001t0029 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1805T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1805 | chr17 | 56889895 | |||||
chr17:56889959
|
C | T | 1 | a0001c0001t0027 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1741G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1741 | chr17 | 56889959 | |||||
chr17:56889994
|
G | C | 1 | a0001c0001t0038 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1706C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1706 | chr17 | 56889994 | |||||
chr17:56890043
|
T | C | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0012others(21): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1657A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1657 | chr17 | 56890043 | |||||
chr17:56890117
|
G | T | 1 | a0001c0001t0026 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1583C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1583 | chr17 | 56890117 | |||||
chr17:56890167
|
A | G | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(35): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1533T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1533 | chr17 | 56890167 | |||||
chr17:56890258
|
A | T | 2 | a0001c0001t0023a0002c0002t0022 | 2 | HG03195.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1442T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1442 | chr17 | 56890258 | |||||
chr17:56890297
|
C | T | 1 | a0001c0014t0025 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1403G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1403 | chr17 | 56890297 | |||||
chr17:56890482
|
A | G | 3 | a0001c0012t0013a0003c0007t0016a0009c0010t0013 | 3 | HG02257.hp1 HG03225.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1218T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1218 | chr17 | 56890482 | |||||
chr17:56890535
|
C | T | 1 | a0001c0001t0024 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1165 | chr17 | 56890535 | |||||
chr17:56890538
|
G | A | 1 | a0001c0001t0039 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1162 | chr17 | 56890538 | |||||
chr17:56890588
|
G | A | 1 | a0001c0001t0005 | 8 | HG01884.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1112C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 1112 | chr17 | 56890588 | |||||
chr17:56890746
|
T | C | 1 | a0002c0002t0040 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*954A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 954 | chr17 | 56890746 | |||||
chr17:56890747
|
T | C | 1 | a0001c0001t0041 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 953 | chr17 | 56890747 | |||||
chr17:56890826
|
T | C | 2 | a0001c0001t0023a0002c0002t0022 | 2 | HG03195.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*874A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 874 | chr17 | 56890826 | |||||
chr17:56890968
|
A | G | 7 | a0001c0001t0011a0001c0001t0023a0001c0012t0013others(4): Show | 8 | HG02257.hp1 HG02486.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*732T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 732 | chr17 | 56890968 | |||||
chr17:56891579
|
C | T | 1 | a0002c0002t0022 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 9/9 | 121 | chr17 | 56891579 | |||||
chr17:56914010
|
A | G | 9 | a0003c0003t0007a0003c0003t0010a0003c0003t0017others(6): Show | 13 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-22T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/9 | 22 | chr17 | 56914010 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:56892373
|
C | A | 8 | a0001c0001t0004g0023a0001c0001t0004g0060a0001c0001t0004g0061others(5): Show | 9 | HG00639.hp1 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364-144G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892373 | ||||||
chr17:56892374
|
CATCT | C | 8 | a0001c0001t0005g0046a0001c0001t0005g0098a0001c0001t0005g0103others(5): Show | 9 | HG01884.hp1 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364-149_1364-146d others(6): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892374 | ||||||
chr17:56892453
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1364-224G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892453 | ||||||
chr17:56892626
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1364-397G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892626 | ||||||
chr17:56892717
|
G | A | 1 | a0003c0003t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1364-488C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892717 | ||||||
chr17:56892768
|
C | G | 3 | a0001c0001t0011g0085a0001c0001t0011g0112a0002c0002t0011g0155 | 3 | HG02486.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1364-539G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892768 | ||||||
chr17:56892820
|
G | T | 110 | a0001c0001t0001g0041a0001c0001t0001g0118a0001c0001t0001g0160others(107): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1364-591C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892820 | ||||||
chr17:56892839
|
C | T | 1 | a0001c0001t0001g0026 | 2 | NA18947.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1364-610G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56892839 | ||||||
chr17:56893220
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1364-991C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893220 | ||||||
chr17:56893223
|
G | GTCTGTAA others(268): Show |
2 | a0001c0012t0013g0090a0009c0010t0013g0108 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1364-995_1364-994i others(277): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893223 | ||||||
chr17:56893224
|
C | T | 2 | a0001c0012t0013g0090a0009c0010t0013g0108 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1364-995G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893224 | ||||||
chr17:56893230
|
T | C | 2 | a0001c0012t0013g0090a0009c0010t0013g0108 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1364-1001A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893230 | ||||||
chr17:56893401
|
G | A | 3 | a0001c0001t0006g0110a0001c0008t0006g0058a0003c0003t0021g0055 | 3 | HG02486.hp1 HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1364-1172C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893401 | ||||||
chr17:56893501
|
A | T | 1 | a0002c0002t0031g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1364-1272T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893501 | ||||||
chr17:56893729
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1364-1500C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893729 | ||||||
chr17:56893782
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1364-1553C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893782 | ||||||
chr17:56893803
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0118a0001c0001t0001g0206others(1): Show | 5 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1363+1540T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893803 | ||||||
chr17:56893880
|
C | A | 165 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0017others(162): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1363+1463G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56893880 | ||||||
chr17:56894093
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1363+1250G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894093 | ||||||
chr17:56894177
|
T | G | 1 | a0001c0001t0027g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1363+1166A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894177 | ||||||
chr17:56894384
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1363+959C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894384 | ||||||
chr17:56894409
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1363+934G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894409 | ||||||
chr17:56894576
|
C | T | 2 | a0001c0001t0001g0026a0001c0014t0025g0088 | 3 | NA18947.hp1 NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1363+767G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894576 | ||||||
chr17:56894651
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1363+692A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894651 | ||||||
chr17:56894842
|
T | C | 1 | a0001c0001t0004g0132 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1363+501A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56894842 | ||||||
chr17:56895003
|
A | G | 2 | a0001c0001t0002g0079a0003c0007t0016g0049 | 2 | HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1363+340T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895003 | ||||||
chr17:56895032
|
C | G | 1 | a0001c0001t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1363+311G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895032 | ||||||
chr17:56895040
|
G | A | 26 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0072others(23): Show | 42 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1363+303C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895040 | ||||||
chr17:56895045
|
C | T | 1 | a0009c0010t0013g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1363+298G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895045 | ||||||
chr17:56895120
|
C | T | 1 | a0002c0002t0001g0179 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1363+223G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895120 | ||||||
chr17:56895121
|
G | T | 1 | a0001c0001t0004g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1363+222C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 8/8 | chr17 | 56895121 | ||||||
chr17:56895696
|
G | A | 1 | a0001c0008t0006g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1181-92C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 6/8 | chr17 | 56895696 | ||||||
chr17:56895750
|
T | A | 2 | a0001c0001t0006g0110a0003c0003t0021g0055 | 2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1181-146A>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 6/8 | chr17 | 56895750 | ||||||
chr17:56895850
|
G | A | 2 | a0002c0002t0022g0092a0006c0015t0002g0216 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1180+76C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 6/8 | chr17 | 56895850 | ||||||
chr17:56895981
|
T | C | 1 | a0002c0002t0022g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1154-29A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56895981 | ||||||
chr17:56896029
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1154-77A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896029 | ||||||
chr17:56896061
|
G | A | 1 | a0001c0001t0004g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1154-109C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896061 | ||||||
chr17:56896160
|
A | C | 1 | a0001c0001t0002g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1154-208T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896160 | ||||||
chr17:56896180
|
A | G | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(67): Show | 100 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1154-228T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896180 | ||||||
chr17:56896322
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1154-370T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896322 | ||||||
chr17:56896347
|
G | GA | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1154-396dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896347 | ||||||
chr17:56896381
|
T | C | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-429A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896381 | ||||||
chr17:56896498
|
C | CA | 5 | a0001c0001t0001g0073a0001c0001t0002g0029a0001c0001t0002g0137others(2): Show | 6 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154-547dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896498 | ||||||
chr17:56896518
|
A | T | 3 | a0002c0002t0002g0040a0002c0002t0002g0069a0002c0002t0011g0155 | 4 | HG02257.hp2 HG02572.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-566T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896518 | ||||||
chr17:56896661
|
C | G | 1 | a0005c0006t0007g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1154-709G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896661 | ||||||
chr17:56896668
|
C | CA | 63 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(60): Show | 129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1154-717dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896668 | ||||||
chr17:56896752
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1154-800C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56896752 | ||||||
chr17:56897049
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1154-1097C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897049 | ||||||
chr17:56897099
|
C | T | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1147G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897099 | ||||||
chr17:56897174
|
G | T | 1 | a0009c0010t0013g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1154-1222C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897174 | ||||||
chr17:56897298
|
C | T | 14 | a0001c0001t0001g0114a0001c0001t0001g0126a0001c0001t0003g0032others(11): Show | 35 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1154-1346G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897298 | ||||||
chr17:56897299
|
G | A | 1 | a0002c0002t0002g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1154-1347C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897299 | ||||||
chr17:56897345
|
C | A | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1393G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897345 | ||||||
chr17:56897346
|
A | G | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1394T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897346 | ||||||
chr17:56897456
|
G | A | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-1504C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897456 | ||||||
chr17:56897662
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0003g0034a0001c0001t0006g0134 | 4 | NA18946.hp1 NA18983.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1453C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897662 | ||||||
chr17:56897817
|
C | T | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1298G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897817 | ||||||
chr17:56897872
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1153+1243G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897872 | ||||||
chr17:56897944
|
G | A | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+1171C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56897944 | ||||||
chr17:56898147
|
G | A | 1 | a0001c0001t0011g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1153+968C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898147 | ||||||
chr17:56898204
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1153+911C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898204 | ||||||
chr17:56898223
|
A | AGTATATG others(12): Show |
4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+873_1153+891d others(21): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898223 | ||||||
chr17:56898261
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1153+854T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898261 | ||||||
chr17:56898298
|
CGGTATAT others(12): Show |
C | 1 | a0001c0001t0001g0136 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1153+798_1153+816d others(21): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898298 | ||||||
chr17:56898317
|
T | TGGTATAT others(12): Show |
1 | a0001c0001t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1153+797_1153+798i others(21): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898317 | ||||||
chr17:56898318
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1153+797C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898318 | ||||||
chr17:56898414
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1153+701G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898414 | ||||||
chr17:56898502
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1153+613T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898502 | ||||||
chr17:56898708
|
C | CA | 21 | a0001c0001t0001g0104a0001c0001t0001g0147a0001c0001t0001g0191others(18): Show | 27 | HG01099.hp1 HG01109.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.1153+406dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898708 | ||||||
chr17:56898770
|
T | G | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+345A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898770 | ||||||
chr17:56898912
|
G | A | 1 | a0001c0001t0008g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1153+203C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898912 | ||||||
chr17:56898943
|
C | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1153+172G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898943 | ||||||
chr17:56898973
|
C | T | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1153+142G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898973 | ||||||
chr17:56898976
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1153+139T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898976 | ||||||
chr17:56898980
|
G | C | 1 | a0002c0002t0002g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1153+135C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56898980 | ||||||
chr17:56899039
|
C | T | 1 | a0001c0001t0002g0028 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1153+76G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 5/8 | chr17 | 56899039 | ||||||
chr17:56899294
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0008g0084 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1088-114G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899294 | ||||||
chr17:56899295
|
G | A | 1 | a0006c0015t0002g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1088-115C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899295 | ||||||
chr17:56899309
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1088-129G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899309 | ||||||
chr17:56899315
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1088-135A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899315 | ||||||
chr17:56899528
|
G | A | 1 | a0001c0001t0004g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1088-348C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899528 | ||||||
chr17:56899561
|
C | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1088-381G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899561 | ||||||
chr17:56899603
|
C | G | 1 | a0005c0006t0007g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1088-423G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899603 | ||||||
chr17:56899687
|
G | A | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-507C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899687 | ||||||
chr17:56899794
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1088-614C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899794 | ||||||
chr17:56899858
|
T | C | 1 | a0002c0002t0002g0175 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1088-678A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56899858 | ||||||
chr17:56900201
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0210 | 3 | NA18998.hp1 NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1088-1021C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900201 | ||||||
chr17:56900208
|
C | T | 1 | a0003c0003t0020g0054 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1088-1028G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900208 | ||||||
chr17:56900209
|
G | A | 6 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179others(3): Show | 10 | NA18940.hp1 NA18964.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088-1029C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900209 | ||||||
chr17:56900213
|
C | CA | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(69): Show | 103 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1088-1034dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900213 | ||||||
chr17:56900213
|
CA | C | 13 | a0002c0002t0001g0008a0002c0002t0001g0062a0002c0002t0001g0063others(10): Show | 33 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1088-1034delT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900213 | ||||||
chr17:56900244
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-1064C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900244 | ||||||
chr17:56900270
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1088-1090G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900270 | ||||||
chr17:56900302
|
A | G | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+1117T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900302 | ||||||
chr17:56900356
|
C | T | 1 | a0001c0001t0005g0098 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1087+1063G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900356 | ||||||
chr17:56900403
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1087+1016C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900403 | ||||||
chr17:56900419
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1087+1000G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900419 | ||||||
chr17:56900746
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1087+673C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900746 | ||||||
chr17:56900938
|
G | A | 1 | a0001c0001t0004g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1087+481C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56900938 | ||||||
chr17:56901020
|
C | T | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+399G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901020 | ||||||
chr17:56901110
|
A | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0094others(7): Show | 11 | HG00280.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1087+309T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901110 | ||||||
chr17:56901193
|
A | C | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+226T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901193 | ||||||
chr17:56901275
|
G | A | 1 | a0002c0002t0040g0180 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1087+144C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901275 | ||||||
chr17:56901332
|
G | A | 3 | a0002c0002t0022g0092a0006c0015t0002g0216a0009c0010t0013g0108 | 3 | HG03195.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1087+87C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901332 | ||||||
chr17:56901358
|
T | G | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+61A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901358 | ||||||
chr17:56901393
|
G | T | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+26C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 4/8 | chr17 | 56901393 | ||||||
chr17:56901767
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.928-189C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901767 | ||||||
chr17:56901787
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.928-209T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901787 | ||||||
chr17:56901873
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928-295C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901873 | ||||||
chr17:56901900
|
T | C | 1 | a0001c0001t0002g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.928-322A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901900 | ||||||
chr17:56901990
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.928-412C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56901990 | ||||||
chr17:56902007
|
G | C | 1 | a0001c0001t0003g0025 | 2 | HG01516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.928-429C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902007 | ||||||
chr17:56902165
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 4 | HG00621.hp2 HG02129.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-587A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902165 | ||||||
chr17:56902171
|
T | C | 1 | a0001c0001t0005g0164 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928-593A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902171 | ||||||
chr17:56902497
|
G | A | 1 | a0006c0015t0002g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-919C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902497 | ||||||
chr17:56902519
|
C | T | 1 | a0001c0001t0005g0046 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.928-941G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902519 | ||||||
chr17:56902642
|
TGCTGGCA others(3): Show |
T | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.928-1074_928-1065d others(12): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902642 | ||||||
chr17:56902654
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.928-1076G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902654 | ||||||
chr17:56902776
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.928-1198G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902776 | ||||||
chr17:56902874
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.928-1296T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56902874 | ||||||
chr17:56903026
|
A | C | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+1229T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903026 | ||||||
chr17:56903034
|
G | A | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+1221C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903034 | ||||||
chr17:56903126
|
C | T | 1 | a0001c0001t0027g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.927+1129G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903126 | ||||||
chr17:56903219
|
G | A | 2 | a0002c0002t0031g0141a0006c0015t0002g0216 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.927+1036C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903219 | ||||||
chr17:56903272
|
C | T | 4 | a0001c0001t0001g0083a0001c0001t0008g0084a0001c0001t0011g0085others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+983G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903272 | ||||||
chr17:56903361
|
A | G | 4 | a0002c0002t0022g0092a0002c0002t0031g0141a0006c0015t0002g0216others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+894T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903361 | ||||||
chr17:56903376
|
C | G | 11 | a0002c0002t0001g0008a0002c0002t0001g0062a0002c0002t0001g0063others(8): Show | 31 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.927+879G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903376 | ||||||
chr17:56903620
|
C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(82): Show | 122 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.927+635G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56903620 | ||||||
chr17:56904210
|
C | CA | 8 | a0001c0001t0001g0106a0001c0001t0002g0077a0001c0001t0002g0140others(5): Show | 8 | HG02071.hp2 HG03516.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+44dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56904210 | ||||||
chr17:56904235
|
A | C | 2 | a0002c0002t0031g0141a0006c0015t0002g0216 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.927+20T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 3/8 | chr17 | 56904235 | ||||||
chr17:56904557
|
G | T | 13 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(10): Show | 18 | HG01099.hp1 HG01109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.694-69C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56904557 | ||||||
chr17:56904608
|
A | G | 2 | a0002c0002t0031g0141a0006c0015t0002g0216 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.694-120T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56904608 | ||||||
chr17:56904988
|
A | G | 1 | a0007c0009t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.694-500T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56904988 | ||||||
chr17:56905227
|
G | A | 1 | a0001c0001t0029g0162 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.694-739C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905227 | ||||||
chr17:56905442
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(66): Show | 100 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.694-954C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905442 | ||||||
chr17:56905569
|
A | G | 2 | a0001c0001t0001g0017a0010c0016t0001g0217 | 4 | NA18945.hp2 NA18948.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-1081T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905569 | ||||||
chr17:56905820
|
G | A | 16 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(13): Show | 21 | HG01099.hp1 HG01109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.694-1332C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905820 | ||||||
chr17:56905869
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.694-1381T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56905869 | ||||||
chr17:56906218
|
A | AG | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.694-1731dupC | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906218 | ||||||
chr17:56906245
|
G | A | 2 | a0001c0001t0037g0089a0001c0012t0013g0090 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.694-1757C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906245 | ||||||
chr17:56906271
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.694-1783T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906271 | ||||||
chr17:56906327
|
A | AC | 12 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0160others(9): Show | 25 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.694-1840dupG | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906327 | ||||||
chr17:56906498
|
A | AT | 33 | a0001c0001t0001g0031a0001c0001t0001g0070a0001c0001t0001g0072others(30): Show | 48 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.693+1969dupA | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906498 | ||||||
chr17:56906605
|
T | C | 1 | a0002c0002t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.693+1863A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906605 | ||||||
chr17:56906648
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(85): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.693+1820G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56906648 | ||||||
chr17:56907029
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.693+1439T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907029 | ||||||
chr17:56907030
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.693+1438C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907030 | ||||||
chr17:56907570
|
T | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 7 | HG00280.hp1 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+898A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907570 | ||||||
chr17:56907809
|
A | G | 15 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(12): Show | 20 | HG01099.hp1 HG01109.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.693+659T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907809 | ||||||
chr17:56907915
|
G | A | 1 | a0001c0001t0001g0019 | 3 | HG02129.hp2 NA18966.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.693+553C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907915 | ||||||
chr17:56907977
|
G | T | 2 | a0002c0002t0022g0092a0009c0010t0013g0108 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.693+491C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56907977 | ||||||
chr17:56908372
|
A | G | 1 | a0006c0015t0002g0216 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.693+96T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56908372 | ||||||
chr17:56908411
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 4 | NA18947.hp2 NA18985.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+57C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 2/8 | chr17 | 56908411 | ||||||
chr17:56909238
|
G | C | 1 | a0001c0001t0002g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.598-675C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909238 | ||||||
chr17:56909471
|
T | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.598-908A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909471 | ||||||
chr17:56909483
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.598-920C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909483 | ||||||
chr17:56909606
|
T | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.598-1043A>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909606 | ||||||
chr17:56909610
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.598-1047C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909610 | ||||||
chr17:56909645
|
A | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0078a0001c0001t0001g0113others(1): Show | 8 | HG00558.hp1 HG00673.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-1082T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909645 | ||||||
chr17:56909684
|
C | CA | 164 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 275 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.598-1122dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909684 | ||||||
chr17:56909919
|
G | A | 13 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(10): Show | 18 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.598-1356C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909919 | ||||||
chr17:56909964
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.598-1401A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56909964 | ||||||
chr17:56910022
|
C | T | 1 | a0002c0002t0003g0022 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.598-1459G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910022 | ||||||
chr17:56910159
|
GA | G | 4 | a0001c0001t0001g0041a0001c0001t0030g0154a0002c0002t0002g0040others(1): Show | 6 | HG02257.hp2 HG02572.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-1597delT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910159 | ||||||
chr17:56910168
|
A | AAC | 12 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(9): Show | 17 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.598-1606_598-1605i others(4): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910168 | ||||||
chr17:56910168
|
A | AC | 3 | a0001c0001t0002g0079a0005c0006t0007g0056a0006c0015t0002g0216 | 3 | HG02615.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.598-1606_598-1605i others(3): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910168 | ||||||
chr17:56910180
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.598-1617C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910180 | ||||||
chr17:56910257
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.598-1694G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910257 | ||||||
chr17:56910349
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.598-1786C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910349 | ||||||
chr17:56910470
|
C | T | 1 | a0001c0001t0003g0025 | 2 | HG01516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.598-1907G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910470 | ||||||
chr17:56910727
|
G | C | 2 | a0002c0002t0022g0092a0009c0010t0013g0108 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.598-2164C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910727 | ||||||
chr17:56910789
|
G | A | 32 | a0001c0001t0001g0027a0001c0001t0001g0094a0001c0001t0001g0095others(29): Show | 38 | HG00280.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.598-2226C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910789 | ||||||
chr17:56910790
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(189): Show | 326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.598-2227T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910790 | ||||||
chr17:56910821
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.598-2258G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910821 | ||||||
chr17:56910880
|
G | A | 15 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(12): Show | 28 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.598-2317C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56910880 | ||||||
chr17:56911140
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.597+2252C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911140 | ||||||
chr17:56911347
|
C | T | 14 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(11): Show | 19 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.597+2045G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911347 | ||||||
chr17:56911398
|
G | A | 1 | a0002c0002t0028g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.597+1994C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911398 | ||||||
chr17:56911472
|
C | T | 1 | a0005c0006t0007g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.597+1920G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911472 | ||||||
chr17:56911494
|
C | T | 19 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(16): Show | 24 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.597+1898G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911494 | ||||||
chr17:56911515
|
G | A | 1 | a0009c0010t0013g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.597+1877C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911515 | ||||||
chr17:56911578
|
C | CA | 108 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(105): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.597+1813dupT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911578 | ||||||
chr17:56911617
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(189): Show | 326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.597+1775T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911617 | ||||||
chr17:56911705
|
T | C | 2 | a0005c0006t0007g0056a0006c0015t0002g0216 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.597+1687A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56911705 | ||||||
chr17:56912002
|
G | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0020others(24): Show | 50 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.597+1390C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912002 | ||||||
chr17:56912046
|
G | A | 12 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(9): Show | 17 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.597+1346C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912046 | ||||||
chr17:56912046
|
GA | G | 2 | a0001c0001t0001g0078a0001c0001t0009g0013 | 5 | HG00558.hp1 NA18971.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+1345delT | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912046 | ||||||
chr17:56912143
|
G | A | 1 | a0002c0002t0002g0204 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.597+1249C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912143 | ||||||
chr17:56912249
|
G | A | 9 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0002g0209others(6): Show | 12 | HG00738.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+1143C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912249 | ||||||
chr17:56912370
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1022G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912370 | ||||||
chr17:56912372
|
A | C | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1020T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912372 | ||||||
chr17:56912374
|
A | C | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1018T>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912374 | ||||||
chr17:56912376
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1016G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912376 | ||||||
chr17:56912378
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1014G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912378 | ||||||
chr17:56912379
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1013T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912379 | ||||||
chr17:56912380
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1012A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912380 | ||||||
chr17:56912382
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1010G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912382 | ||||||
chr17:56912384
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1008G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912384 | ||||||
chr17:56912385
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1007T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912385 | ||||||
chr17:56912386
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1006T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912386 | ||||||
chr17:56912387
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1005T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912387 | ||||||
chr17:56912389
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1003A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912389 | ||||||
chr17:56912390
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1002G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912390 | ||||||
chr17:56912391
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1001T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912391 | ||||||
chr17:56912392
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+1000G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912392 | ||||||
chr17:56912393
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+999T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912393 | ||||||
chr17:56912394
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+998G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912394 | ||||||
chr17:56912397
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+995G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912397 | ||||||
chr17:56912398
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+994G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912398 | ||||||
chr17:56912399
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+993T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912399 | ||||||
chr17:56912402
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+990T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912402 | ||||||
chr17:56912403
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+989G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912403 | ||||||
chr17:56912406
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+986T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912406 | ||||||
chr17:56912409
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+983T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912409 | ||||||
chr17:56912410
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+982G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912410 | ||||||
chr17:56912411
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+981T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912411 | ||||||
chr17:56912412
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+980G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912412 | ||||||
chr17:56912413
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+979A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912413 | ||||||
chr17:56912414
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+978T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912414 | ||||||
chr17:56912415
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.597+977A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912415 | ||||||
chr17:56912458
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.597+934A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912458 | ||||||
chr17:56912467
|
C | T | 14 | a0001c0001t0002g0016a0001c0001t0002g0075a0001c0001t0002g0077others(11): Show | 19 | HG01099.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.597+925G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912467 | ||||||
chr17:56912509
|
C | G | 1 | a0001c0001t0002g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.597+883G>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912509 | ||||||
chr17:56912530
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG02258.hp1 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+862G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912530 | ||||||
chr17:56912813
|
T | G | 1 | a0001c0001t0008g0212 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.597+579A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912813 | ||||||
chr17:56912838
|
A | ATTTGAAT others(3): Show |
1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+553_597+554ins others(10): Show |
TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912838 | ||||||
chr17:56912842
|
A | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+550T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912842 | ||||||
chr17:56912844
|
C | A | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+548G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912844 | ||||||
chr17:56912845
|
A | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+547T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912845 | ||||||
chr17:56912846
|
T | G | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+546A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912846 | ||||||
chr17:56912850
|
A | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+542T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912850 | ||||||
chr17:56912857
|
G | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+535C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912857 | ||||||
chr17:56912858
|
G | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+534C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912858 | ||||||
chr17:56912859
|
C | A | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+533G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912859 | ||||||
chr17:56912859
|
C | T | 1 | a0001c0001t0003g0025 | 2 | HG01516.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.597+533G>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912859 | ||||||
chr17:56912860
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.597+532C>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912860 | ||||||
chr17:56912860
|
G | C | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+532C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912860 | ||||||
chr17:56912862
|
A | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+530T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912862 | ||||||
chr17:56912863
|
G | C | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+529C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912863 | ||||||
chr17:56912866
|
G | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+526C>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912866 | ||||||
chr17:56912872
|
G | C | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+520C>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912872 | ||||||
chr17:56912876
|
T | C | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+516A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912876 | ||||||
chr17:56912877
|
T | C | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+515A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912877 | ||||||
chr17:56912878
|
A | G | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+514T>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912878 | ||||||
chr17:56912882
|
A | T | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+510T>A | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912882 | ||||||
chr17:56912888
|
T | G | 1 | a0001c0001t0005g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597+504A>C | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56912888 | ||||||
chr17:56913008
|
T | C | 9 | a0003c0003t0007g0021a0003c0003t0007g0053a0003c0003t0010g0015others(6): Show | 12 | HG02257.hp1 HG02451.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.597+384A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913008 | ||||||
chr17:56913258
|
T | C | 1 | a0002c0002t0002g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.597+134A>G | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913258 | ||||||
chr17:56913291
|
C | CT | 17 | a0001c0001t0004g0023a0001c0001t0004g0060a0001c0001t0004g0061others(14): Show | 38 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.597+100dupA | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913291 | ||||||
chr17:56913343
|
C | A | 2 | a0005c0006t0007g0056a0006c0015t0002g0216 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.597+49G>T | TRIM25 | ENSG00000121060.19 | transcript | ENST00000316881.9 | protein_coding | 1/8 | chr17 | 56913343 |