geneid | 55223 |
---|---|
ensemblid | ENSG00000116525.14 |
hgncid | 25574 |
symbol | TRIM62 |
name | tripartite motif containing 62 |
refseq_nuc | NM_018207.3 |
refseq_prot | NP_060677.2 |
ensembl_nuc | ENST00000291416.10 |
ensembl_prot | ENSP00000291416.5 |
mane_status | MANE Select |
chr | chr1 |
start | 33145399 |
end | 33182043 |
strand | - |
ver | v1.2 |
region | chr1:33145399-33182043 |
region5000 | chr1:33140399-33187043 |
regionname0 | TRIM62_chr1_33145399_33182043 |
regionname5000 | TRIM62_chr1_33140399_33187043 |
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 | 1/1 | 475 | 325 | 78 | 52 | 149 | 10 | 34 | 109 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0002 | 0/0 | 475 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0003 | 0/0 | 475 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0004 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
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 | 0/1 | 1428 | 224 | 53 | 37 | 104 | 6 | 23 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0002 | 1/0 | 1428 | 87 | 14 | 15 | 43 | 4 | 10 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0003 | 0/0 | 1428 | 12 | 12 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0004 | 0/0 | 1428 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0005 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0006 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0007 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0008 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0009 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0010 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0011 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0012 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0013 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
c0014 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
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 | 0/1 | 2390 | 191 | 48 | 38 | 77 | 6 | 21 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0002 | 0/0 | 2390 | 63 | 2 | 11 | 36 | 4 | 10 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0003 | 1/0 | 2390 | 57 | 20 | 2 | 31 | 0 | 3 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0004 | 0/0 | 2390 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0005 | 0/0 | 2390 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0006 | 0/0 | 2390 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0007 | 0/0 | 2390 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0008 | 0/0 | 2390 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0009 | 0/0 | 2390 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0010 | 0/0 | 2390 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0011 | 0/0 | 2390 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0012 | 0/0 | 2390 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0013 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0014 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0015 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0016 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0017 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
t0018 | 0/0 | 2390 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
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 | 28 | 1 | 3 | 18 | 3 | 3 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0002 | 0/0 | 10 | 1 | 3 | 5 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0003 | 0/1 | 8 | 0 | 3 | 3 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0008 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0009 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
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 | 0/1 | 1428 | 224 | 53 | 37 | 104 | 6 | 23 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002 | 1/0 | 1428 | 87 | 14 | 15 | 43 | 4 | 10 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0004 | 0/0 | 1428 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0006 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0007 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0008 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0009 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0011 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0012 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0013 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0014 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0002c0003 | 0/0 | 1428 | 12 | 12 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0003c0005 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0004c0010 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3817 | 182 | 46 | 36 | 73 | 6 | 20 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0002 | 0/0 | 3817 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0003 | 0/0 | 3817 | 28 | 4 | 0 | 21 | 0 | 3 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0005 | 0/0 | 3817 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0006 | 0/0 | 3817 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0007 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0008 | 0/0 | 3817 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0011 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0001t0012 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0001 | 0/0 | 3817 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0002 | 0/0 | 3817 | 58 | 1 | 10 | 33 | 4 | 10 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0003 | 1/0 | 3817 | 19 | 6 | 2 | 10 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0009 | 0/0 | 3817 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0010 | 0/0 | 3817 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0016 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0017 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0002t0018 | 0/0 | 3817 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0004t0003 | 0/0 | 3817 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0004t0007 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0006t0003 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0007t0014 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0008t0001 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0009t0001 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0011t0001 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0012t0015 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0013t0002 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0001c0014t0002 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0002c0003t0003 | 0/0 | 3817 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0002c0003t0004 | 0/0 | 3817 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0002c0003t0013 | 0/0 | 3817 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0003c0005t0001 | 0/0 | 3817 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
a0004c0010t0001 | 0/0 | 3817 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | copy fasta | chr1 | 33140399 | 33187043 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 10 | 1 | 3 | 5 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0003 | 0/1 | 8 | 0 | 3 | 3 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0008 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0001t0012g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0001 | 0/0 | 28 | 1 | 3 | 18 | 3 | 3 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0016g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0017g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0002t0018g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0004t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0004t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0004t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0004t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0006t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0007t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0008t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0011t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0012t0015g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0013t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0001c0014t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0002c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0002c0003t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0002c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0002c0003t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0002c0003t0004g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0002c0003t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0002c0003t0013g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0003c0005t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
a0004c0010t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | FIN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00408 | hp2 | a0001 | c0013 | t0002 | g0188 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00544 | hp2 | a0001 | c0001 | t0011 | g0146 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0214 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01109 | hp2 | a0001 | c0002 | t0018 | g0231 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0207 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0215 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0187 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01884 | hp1 | a0001 | c0002 | t0016 | g0229 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0211 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01891 | hp2 | a0002 | c0003 | t0004 | g0004 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0200 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | CDX | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02451 | hp1 | a0001 | c0002 | t0009 | g0182 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02622 | hp2 | a0001 | c0002 | t0017 | g0230 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02630 | hp1 | a0002 | c0003 | t0003 | g0221 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0045 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02818 | hp1 | a0001 | c0002 | t0003 | g0218 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02818 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02896 | hp1 | a0001 | c0002 | t0010 | g0233 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02897 | hp1 | a0001 | c0002 | t0010 | g0232 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02922 | hp1 | a0001 | c0004 | t0003 | g0070 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02922 | hp2 | a0001 | c0006 | t0003 | g0175 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03130 | hp1 | a0002 | c0003 | t0013 | g0224 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03139 | hp1 | a0001 | c0004 | t0003 | g0071 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03195 | hp2 | a0002 | c0003 | t0004 | g0004 | AFR | ESN | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03209 | hp1 | a0002 | c0003 | t0004 | g0004 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0186 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0045 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03540 | hp1 | a0001 | c0011 | t0001 | g0220 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03540 | hp2 | a0002 | c0003 | t0004 | g0004 | AFR | GWD | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03710 | hp2 | a0001 | c0008 | t0001 | g0130 | SAS | PJL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0201 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0185 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0184 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | BEB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18522 | hp1 | a0001 | c0007 | t0014 | g0227 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18522 | hp2 | a0002 | c0003 | t0004 | g0004 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18747 | hp2 | a0001 | c0001 | t0012 | g0135 | EAS | CHB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18906 | hp1 | a0002 | c0003 | t0003 | g0217 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18906 | hp2 | a0001 | c0002 | t0009 | g0181 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18960 | hp1 | a0003 | c0005 | t0001 | g0030 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18966 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18967 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18988 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA18998 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19002 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19004 | hp1 | a0001 | c0009 | t0001 | g0094 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19030 | hp1 | a0002 | c0003 | t0003 | g0223 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19043 | hp1 | a0001 | c0014 | t0002 | g0183 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19054 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19079 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19090 | hp1 | a0003 | c0005 | t0001 | g0030 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19091 | hp2 | a0004 | c0010 | t0001 | g0179 | EAS | JPT | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19240 | hp1 | a0002 | c0003 | t0004 | g0004 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA19240 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | YRI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0219 | AFR | ASW | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02109 | hp1 | a0001 | c0004 | t0007 | g0155 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02109 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02486 | hp2 | a0002 | c0003 | t0003 | g0225 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0216 | AFR | MSL | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
HG06807 | hp2 | a0001 | c0012 | t0015 | g0228 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | USA | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
NA21309 | hp2 | a0002 | c0003 | t0004 | g0222 | AFR | LWK | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0210 | REF | REF | TRIM62_chr1_33140399_33187043 | TRIM62 | chr1 | 33140399 | 33187043 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:33147188
|
C | T | 1 | a0002 | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
missense_variant | MODERATE | c.1417G>A | p.Val473Ile | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 2028/3817 | 1417/1428 | 473/475 | chr1 | 33147188 | ||
chr1:33159844
|
G | A | 1 | a0003 | 2 | NA18960.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.605C>T | p.Ala202Val | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1216/3817 | 605/1428 | 202/475 | chr1 | 33159844 | ||
chr1:33181158
|
G | A | 1 | a0004 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.275C>T | p.Pro92Leu | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 886/3817 | 275/1428 | 92/475 | chr1 | 33181158 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:33147414
|
G | A | 1 | a0001c0008 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1191C>T | p.Tyr397Tyr | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1802/3817 | 1191/1428 | 397/475 | chr1 | 33147414 | ||
chr1:33147453
|
G | A | 1 | a0001c0009 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.1152C>T | p.Arg384Arg | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1763/3817 | 1152/1428 | 384/475 | chr1 | 33147453 | ||
chr1:33147585
|
C | G | 1 | a0001c0006 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1020G>C | p.Val340Val | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1631/3817 | 1020/1428 | 340/475 | chr1 | 33147585 | ||
chr1:33147672
|
C | T | 1 | a0001c0007 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.933G>A | p.Ser311Ser | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1544/3817 | 933/1428 | 311/475 | chr1 | 33147672 | ||
chr1:33158302
|
G | A | 1 | a0001c0011 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.828C>T | p.Gly276Gly | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/5 | 1439/3817 | 828/1428 | 276/475 | chr1 | 33158302 | ||
chr1:33159747
|
C | T | 2 | a0001c0004a0001c0006 | 7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
synonymous_variant | LOW | c.702G>A | p.Glu234Glu | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1313/3817 | 702/1428 | 234/475 | chr1 | 33159747 | ||
chr1:33159822
|
G | A | 1 | a0001c0012 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.627C>T | p.Thr209Thr | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1238/3817 | 627/1428 | 209/475 | chr1 | 33159822 | ||
chr1:33159834
|
G | C | 1 | a0001c0013 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.615C>G | p.Ala205Ala | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1226/3817 | 615/1428 | 205/475 | chr1 | 33159834 | ||
chr1:33159903
|
G | A | 1 | a0001c0014 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.546C>T | p.Phe182Phe | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/5 | 1157/3817 | 546/1428 | 182/475 | chr1 | 33159903 | ||
chr1:33181349
|
A | G | 8 | a0001c0001a0001c0004a0001c0006others(5): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
synonymous_variant | LOW | c.84T>C | p.His28His | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 695/3817 | 84/1428 | 28/475 | chr1 | 33181349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:33145432
|
T | C | 1 | a0001c0001t0005 | 4 | NA18948.hp1 NA18967.hp1 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1745A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1745 | chr1 | 33145432 | |||||
chr1:33145583
|
G | A | 2 | a0002c0003t0004a0002c0003t0013 | 8 | HG01891.hp2 HG03130.hp1 HG03195.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1594C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1594 | chr1 | 33145583 | |||||
chr1:33145749
|
G | A | 3 | a0001c0001t0008a0001c0002t0009a0001c0002t0010 | 6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1428C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1428 | chr1 | 33145749 | |||||
chr1:33145853
|
T | C | 1 | a0001c0001t0012 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 1324 | chr1 | 33145853 | |||||
chr1:33146289
|
C | T | 14 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(11): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 888 | chr1 | 33146289 | |||||
chr1:33146386
|
G | A | 1 | a0001c0002t0009 | 2 | HG02451.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*791C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 791 | chr1 | 33146386 | |||||
chr1:33146597
|
A | G | 2 | a0001c0001t0007a0001c0004t0007 | 2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*580T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 580 | chr1 | 33146597 | |||||
chr1:33146599
|
C | T | 1 | a0001c0001t0006 | 2 | NA19079.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 578 | chr1 | 33146599 | |||||
chr1:33146619
|
T | C | 1 | a0002c0003t0013 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 558 | chr1 | 33146619 | |||||
chr1:33146863
|
G | A | 1 | a0001c0012t0015 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 314 | chr1 | 33146863 | |||||
chr1:33146907
|
G | A | 4 | a0001c0001t0002a0001c0002t0002a0001c0013t0002others(1): Show | 63 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 270 | chr1 | 33146907 | |||||
chr1:33146985
|
C | T | 1 | a0001c0001t0011 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*192G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 5/5 | 192 | chr1 | 33146985 | |||||
chr1:33181533
|
G | A | 1 | a0001c0007t0014 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-101C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 101 | chr1 | 33181533 | |||||
chr1:33181787
|
C | T | 1 | a0001c0002t0016 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-355G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 355 | chr1 | 33181787 | |||||
chr1:33181894
|
G | A | 1 | a0001c0012t0015 | 1 | HG06807.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-462C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | chr1 | 33181894 | ||||||
chr1:33181949
|
C | A | 4 | a0001c0002t0010a0001c0002t0016a0001c0002t0017others(1): Show | 5 | HG01109.hp2 HG01884.hp1 HG02622.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-517G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/5 | 517 | chr1 | 33181949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:33147883
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.878-156G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33147883 | ||||||
chr1:33148149
|
A | G | 1 | a0001c0001t0003g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.878-422T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148149 | ||||||
chr1:33148180
|
G | A | 1 | a0004c0010t0001g0179 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.878-453C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148180 | ||||||
chr1:33148561
|
T | C | 51 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(48): Show | 88 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.878-834A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148561 | ||||||
chr1:33148767
|
T | C | 5 | a0001c0001t0008g0016a0001c0002t0009g0181a0001c0002t0009g0182others(2): Show | 6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-1040A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148767 | ||||||
chr1:33148781
|
A | T | 1 | a0001c0004t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-1054T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148781 | ||||||
chr1:33148887
|
A | T | 4 | a0001c0004t0003g0010a0001c0004t0003g0070a0001c0004t0003g0071others(1): Show | 6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-1160T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33148887 | ||||||
chr1:33149064
|
A | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(163): Show | 230 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.878-1337T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149064 | ||||||
chr1:33149110
|
G | T | 3 | a0001c0001t0008g0016a0001c0002t0010g0232a0001c0002t0010g0233 | 4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-1383C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149110 | ||||||
chr1:33149161
|
T | G | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.878-1434A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149161 | ||||||
chr1:33149199
|
C | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(163): Show | 230 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.878-1472G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149199 | ||||||
chr1:33149403
|
C | T | 7 | a0002c0003t0003g0217a0002c0003t0003g0221a0002c0003t0003g0223others(4): Show | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.878-1676G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149403 | ||||||
chr1:33149405
|
C | T | 5 | a0001c0002t0003g0211a0001c0004t0003g0010a0001c0004t0003g0070others(2): Show | 7 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.878-1678G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149405 | ||||||
chr1:33149457
|
T | TA | 30 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(27): Show | 63 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.878-1731_878-1730i others(3): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149457 | ||||||
chr1:33149458
|
T | A | 33 | a0001c0001t0001g0145a0001c0001t0002g0099a0001c0001t0002g0176others(30): Show | 66 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.878-1731A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149458 | ||||||
chr1:33149458
|
T | TA | 18 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(15): Show | 22 | HG00597.hp1 HG00673.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.878-1732dupT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149458 | ||||||
chr1:33149636
|
A | G | 31 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(28): Show | 64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.878-1909T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149636 | ||||||
chr1:33149697
|
C | G | 20 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(17): Show | 26 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.878-1970G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149697 | ||||||
chr1:33149792
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.878-2065C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149792 | ||||||
chr1:33149994
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.878-2267G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33149994 | ||||||
chr1:33150007
|
G | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0117a0001c0001t0001g0147others(2): Show | 6 | HG00544.hp2 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-2280C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150007 | ||||||
chr1:33150015
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.878-2288G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150015 | ||||||
chr1:33150186
|
G | C | 1 | a0001c0002t0003g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.878-2459C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150186 | ||||||
chr1:33150275
|
A | G | 31 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(28): Show | 64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.878-2548T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150275 | ||||||
chr1:33150292
|
TCTCCCTA | T | 5 | a0002c0003t0003g0223a0002c0003t0003g0225a0002c0003t0004g0004others(2): Show | 10 | HG01891.hp2 HG02486.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-2572_878-2566d others(9): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150292 | ||||||
chr1:33150612
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.878-2885G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150612 | ||||||
chr1:33150648
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.878-2921C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150648 | ||||||
chr1:33150649
|
G | T | 1 | a0001c0002t0002g0203 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.878-2922C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150649 | ||||||
chr1:33150707
|
G | A | 1 | a0001c0004t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-2980C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150707 | ||||||
chr1:33150709
|
C | G | 49 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(46): Show | 86 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.878-2982G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150709 | ||||||
chr1:33150722
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0048 | 3 | HG02280.hp2 HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.878-2995C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150722 | ||||||
chr1:33150864
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(222): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.878-3137A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33150864 | ||||||
chr1:33151013
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.878-3286G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151013 | ||||||
chr1:33151108
|
G | A | 1 | a0001c0002t0009g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.878-3381C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151108 | ||||||
chr1:33151150
|
G | C | 50 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(47): Show | 87 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.878-3423C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151150 | ||||||
chr1:33151185
|
T | C | 1 | a0001c0002t0003g0194 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.878-3458A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151185 | ||||||
chr1:33151321
|
C | T | 1 | a0001c0012t0015g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.878-3594G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151321 | ||||||
chr1:33151356
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0087 | 2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.878-3629G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151356 | ||||||
chr1:33151366
|
T | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0080others(4): Show | 10 | HG00741.hp1 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-3639A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151366 | ||||||
chr1:33151542
|
T | C | 1 | a0001c0002t0009g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.878-3815A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151542 | ||||||
chr1:33151657
|
G | A | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.878-3930C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151657 | ||||||
chr1:33151709
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.878-3982G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151709 | ||||||
chr1:33151747
|
A | G | 20 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(17): Show | 26 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.878-4020T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151747 | ||||||
chr1:33151799
|
A | T | 1 | a0001c0004t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-4072T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151799 | ||||||
chr1:33151809
|
C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.878-4082G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151809 | ||||||
chr1:33151860
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.878-4133G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151860 | ||||||
chr1:33151978
|
T | C | 10 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(7): Show | 14 | HG02080.hp2 HG03710.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.878-4251A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33151978 | ||||||
chr1:33152303
|
C | T | 1 | a0001c0001t0001g0026 | 2 | NA18983.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.878-4576G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152303 | ||||||
chr1:33152337
|
A | C | 7 | a0002c0003t0003g0217a0002c0003t0003g0221a0002c0003t0003g0223others(4): Show | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.878-4610T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152337 | ||||||
chr1:33152422
|
C | T | 2 | a0001c0001t0006g0139a0001c0001t0006g0151 | 2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.878-4695G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152422 | ||||||
chr1:33152425
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.878-4698G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152425 | ||||||
chr1:33152431
|
G | T | 3 | a0001c0004t0003g0070a0001c0004t0003g0071a0001c0006t0003g0175 | 3 | HG02922.hp1 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.878-4704C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152431 | ||||||
chr1:33152466
|
C | T | 1 | a0001c0004t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878-4739G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152466 | ||||||
chr1:33152482
|
G | A | 7 | a0002c0003t0003g0217a0002c0003t0003g0221a0002c0003t0003g0223others(4): Show | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.878-4755C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152482 | ||||||
chr1:33152506
|
G | A | 1 | a0001c0001t0001g0012 | 3 | HG02071.hp1 NA18957.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.878-4779C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152506 | ||||||
chr1:33152554
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(229): Show | 339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.878-4827A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152554 | ||||||
chr1:33152573
|
G | GA | 22 | a0001c0001t0001g0058a0001c0001t0001g0082a0001c0001t0001g0104others(19): Show | 25 | HG00597.hp1 HG00673.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.878-4847dupT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152573 | ||||||
chr1:33152573
|
GA | G | 38 | a0001c0001t0001g0036a0001c0001t0001g0048a0001c0001t0001g0096others(35): Show | 73 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.878-4847delT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152573 | ||||||
chr1:33152812
|
C | T | 36 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(33): Show | 70 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.878-5085G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152812 | ||||||
chr1:33152869
|
G | C | 1 | a0001c0002t0003g0195 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.878-5142C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152869 | ||||||
chr1:33152899
|
C | T | 5 | a0001c0002t0003g0211a0001c0004t0003g0010a0001c0004t0003g0070others(2): Show | 7 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.878-5172G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33152899 | ||||||
chr1:33153015
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 6 | HG01891.hp1 HG01934.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.877+5238T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153015 | ||||||
chr1:33153038
|
G | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.877+5215C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153038 | ||||||
chr1:33153297
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0060others(3): Show | 8 | HG00639.hp2 HG01070.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.877+4956G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153297 | ||||||
chr1:33153561
|
A | G | 1 | a0001c0002t0002g0201 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.877+4692T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33153561 | ||||||
chr1:33154134
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.877+4119T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154134 | ||||||
chr1:33154259
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(227): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.877+3994T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154259 | ||||||
chr1:33154508
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.877+3745A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154508 | ||||||
chr1:33154603
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.877+3650G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154603 | ||||||
chr1:33154603
|
C | T | 4 | a0001c0004t0003g0010a0001c0004t0003g0070a0001c0004t0003g0071others(1): Show | 6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+3650G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154603 | ||||||
chr1:33154609
|
C | A | 2 | a0001c0001t0001g0178a0001c0001t0011g0146 | 2 | HG00544.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.877+3644G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154609 | ||||||
chr1:33154965
|
T | C | 53 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(50): Show | 92 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.877+3288A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33154965 | ||||||
chr1:33155041
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.877+3212G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155041 | ||||||
chr1:33155078
|
G | A | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+3175C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155078 | ||||||
chr1:33155098
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.877+3155C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155098 | ||||||
chr1:33155102
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0117a0001c0001t0001g0147others(5): Show | 9 | HG00544.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.877+3151G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155102 | ||||||
chr1:33155135
|
G | A | 1 | a0002c0003t0003g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.877+3118C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155135 | ||||||
chr1:33155314
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.877+2939G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155314 | ||||||
chr1:33155356
|
C | A | 2 | a0001c0002t0010g0232a0001c0002t0010g0233 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.877+2897G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155356 | ||||||
chr1:33155366
|
C | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0068a0001c0001t0001g0069others(7): Show | 11 | HG00544.hp2 HG02145.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.877+2887G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155366 | ||||||
chr1:33155408
|
T | C | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+2845A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155408 | ||||||
chr1:33155530
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.877+2723T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155530 | ||||||
chr1:33155547
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.877+2706C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155547 | ||||||
chr1:33155569
|
G | A | 2 | a0001c0001t0003g0148a0001c0002t0003g0218 | 2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.877+2684C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155569 | ||||||
chr1:33155782
|
T | C | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+2471A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33155782 | ||||||
chr1:33156063
|
G | T | 1 | a0001c0004t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.877+2190C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156063 | ||||||
chr1:33156085
|
C | T | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+2168G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156085 | ||||||
chr1:33156142
|
A | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(227): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.877+2111T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156142 | ||||||
chr1:33156236
|
A | G | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.877+2017T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156236 | ||||||
chr1:33156283
|
T | G | 1 | a0002c0003t0003g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.877+1970A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156283 | ||||||
chr1:33156472
|
G | C | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.877+1781C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156472 | ||||||
chr1:33156476
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(222): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.877+1777A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156476 | ||||||
chr1:33156493
|
C | T | 2 | a0001c0001t0003g0148a0001c0002t0003g0218 | 2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.877+1760G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156493 | ||||||
chr1:33156523
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.877+1730A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156523 | ||||||
chr1:33156681
|
T | C | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+1572A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156681 | ||||||
chr1:33156756
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.877+1497A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156756 | ||||||
chr1:33156876
|
C | T | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+1377G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33156876 | ||||||
chr1:33157018
|
C | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0134a0001c0001t0012g0135 | 4 | HG00609.hp2 HG02129.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+1235G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157018 | ||||||
chr1:33157038
|
C | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0059others(5): Show | 10 | HG00639.hp2 HG01070.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.877+1215G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157038 | ||||||
chr1:33157105
|
G | A | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.877+1148C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157105 | ||||||
chr1:33157127
|
C | T | 2 | a0001c0002t0002g0044a0001c0013t0002g0188 | 3 | HG00408.hp2 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.877+1126G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157127 | ||||||
chr1:33157428
|
C | T | 1 | a0001c0014t0002g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.877+825G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157428 | ||||||
chr1:33157491
|
C | G | 2 | a0001c0002t0010g0232a0001c0002t0010g0233 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.877+762G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157491 | ||||||
chr1:33157544
|
T | G | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+709A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157544 | ||||||
chr1:33157545
|
C | T | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+708G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157545 | ||||||
chr1:33157554
|
A | G | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0002t0001g0180others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.877+699T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157554 | ||||||
chr1:33157555
|
T | A | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.877+698A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157555 | ||||||
chr1:33157775
|
G | A | 6 | a0001c0001t0003g0127a0001c0001t0003g0156a0001c0001t0003g0158others(3): Show | 6 | HG01109.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.877+478C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157775 | ||||||
chr1:33157833
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.877+420A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157833 | ||||||
chr1:33157882
|
G | A | 12 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(9): Show | 15 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.877+371C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157882 | ||||||
chr1:33157904
|
A | T | 4 | a0001c0004t0003g0010a0001c0004t0003g0070a0001c0004t0003g0071others(1): Show | 6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+349T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157904 | ||||||
chr1:33157909
|
A | G | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(17): Show | 32 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.877+344T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157909 | ||||||
chr1:33157976
|
C | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0177 | 2 | HG02083.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.877+277G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33157976 | ||||||
chr1:33158047
|
G | A | 1 | a0001c0012t0015g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.877+206C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33158047 | ||||||
chr1:33158047
|
G | C | 1 | a0002c0003t0003g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.877+206C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 4/4 | chr1 | 33158047 | ||||||
chr1:33158421
|
A | G | 2 | a0001c0001t0001g0081a0001c0002t0003g0196 | 2 | NA18988.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.762-53T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158421 | ||||||
chr1:33158428
|
G | C | 2 | a0001c0001t0003g0148a0001c0002t0003g0218 | 2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.762-60C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158428 | ||||||
chr1:33158434
|
C | T | 1 | a0002c0003t0003g0225 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.762-66G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158434 | ||||||
chr1:33158441
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.762-73T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158441 | ||||||
chr1:33158443
|
C | T | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.762-75G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158443 | ||||||
chr1:33158846
|
C | CT | 7 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0106others(4): Show | 7 | HG00741.hp1 HG00741.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-479dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158846 | ||||||
chr1:33158997
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.762-629G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33158997 | ||||||
chr1:33159093
|
C | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0090 | 3 | HG03239.hp2 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.761+595G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159093 | ||||||
chr1:33159097
|
G | A | 7 | a0002c0003t0003g0217a0002c0003t0003g0221a0002c0003t0003g0223others(4): Show | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.761+591C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159097 | ||||||
chr1:33159099
|
C | T | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.761+589G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159099 | ||||||
chr1:33159122
|
G | T | 1 | a0001c0002t0002g0200 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.761+566C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159122 | ||||||
chr1:33159144
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.761+544T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159144 | ||||||
chr1:33159247
|
G | C | 2 | a0001c0002t0002g0205a0001c0002t0002g0206 | 2 | NA18960.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.761+441C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159247 | ||||||
chr1:33159456
|
G | A | 1 | a0001c0002t0003g0197 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.761+232C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159456 | ||||||
chr1:33159569
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.761+119T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159569 | ||||||
chr1:33159674
|
C | T | 2 | a0001c0002t0002g0192a0001c0002t0002g0199 | 2 | HG01074.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.761+14G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159674 | ||||||
chr1:33159675
|
G | A | 2 | a0001c0001t0003g0158a0001c0001t0003g0161 | 2 | NA19058.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.761+13C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 3/4 | chr1 | 33159675 | ||||||
chr1:33160059
|
C | G | 1 | a0001c0012t0015g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.505-115G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160059 | ||||||
chr1:33160408
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0093 | 2 | NA18962.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.505-464T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160408 | ||||||
chr1:33160413
|
T | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.505-469A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160413 | ||||||
chr1:33160493
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG00408.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.505-549G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160493 | ||||||
chr1:33160518
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0001g0092others(2): Show | 6 | HG00438.hp2 HG02040.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-574G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160518 | ||||||
chr1:33160553
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 90 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.505-609G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160553 | ||||||
chr1:33160597
|
G | A | 5 | a0001c0001t0008g0016a0001c0002t0009g0181a0001c0002t0009g0182others(2): Show | 6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-653C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160597 | ||||||
chr1:33160636
|
G | C | 36 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(33): Show | 71 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.505-692C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160636 | ||||||
chr1:33160683
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.505-739C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160683 | ||||||
chr1:33160684
|
C | T | 1 | a0001c0006t0003g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.505-740G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160684 | ||||||
chr1:33160690
|
C | G | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.505-746G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160690 | ||||||
chr1:33160974
|
A | G | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-1030T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33160974 | ||||||
chr1:33161003
|
C | T | 17 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(14): Show | 23 | HG01884.hp2 HG02080.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.505-1059G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161003 | ||||||
chr1:33161080
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.505-1136A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161080 | ||||||
chr1:33161162
|
C | T | 12 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(9): Show | 15 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.505-1218G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161162 | ||||||
chr1:33161212
|
G | A | 5 | a0001c0001t0001g0078a0001c0001t0003g0127a0001c0001t0003g0158others(2): Show | 5 | HG02886.hp2 HG03704.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-1268C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161212 | ||||||
chr1:33161232
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG01123.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.505-1288C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161232 | ||||||
chr1:33161342
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.505-1398T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161342 | ||||||
chr1:33161421
|
G | A | 1 | a0001c0012t0015g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.505-1477C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161421 | ||||||
chr1:33161592
|
G | A | 5 | a0001c0004t0003g0010a0001c0004t0003g0070a0001c0004t0003g0071others(2): Show | 7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-1648C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161592 | ||||||
chr1:33161648
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.505-1704G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161648 | ||||||
chr1:33161656
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0088 | 5 | HG00621.hp1 HG02165.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-1712G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161656 | ||||||
chr1:33161697
|
G | A | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-1753C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161697 | ||||||
chr1:33161723
|
C | A | 5 | a0001c0004t0003g0010a0001c0004t0003g0070a0001c0004t0003g0071others(2): Show | 7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-1779G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161723 | ||||||
chr1:33161810
|
C | G | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.505-1866G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161810 | ||||||
chr1:33161823
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(146): Show | 207 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.505-1879A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161823 | ||||||
chr1:33161916
|
C | T | 3 | a0001c0001t0008g0016a0001c0002t0010g0232a0001c0002t0010g0233 | 4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-1972G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161916 | ||||||
chr1:33161930
|
C | T | 2 | a0001c0001t0006g0139a0001c0001t0006g0151 | 2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.505-1986G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33161930 | ||||||
chr1:33162056
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 6 | HG01069.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2112G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162056 | ||||||
chr1:33162197
|
A | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(209): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.505-2253T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162197 | ||||||
chr1:33162317
|
C | A | 1 | a0001c0002t0009g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.505-2373G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162317 | ||||||
chr1:33162426
|
T | G | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.505-2482A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162426 | ||||||
chr1:33162563
|
C | T | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.505-2619G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162563 | ||||||
chr1:33162674
|
G | A | 2 | a0001c0002t0010g0232a0001c0002t0010g0233 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.505-2730C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162674 | ||||||
chr1:33162740
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.504+2731T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162740 | ||||||
chr1:33162934
|
T | C | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.504+2537A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33162934 | ||||||
chr1:33163094
|
A | AC | 10 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(7): Show | 14 | HG02080.hp2 HG03710.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.504+2376_504+2377i others(3): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163094 | ||||||
chr1:33163095
|
G | A | 10 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(7): Show | 14 | HG02080.hp2 HG03710.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.504+2376C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163095 | ||||||
chr1:33163101
|
C | T | 1 | a0001c0002t0003g0045 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.504+2370G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163101 | ||||||
chr1:33163323
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.504+2148C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163323 | ||||||
chr1:33163327
|
C | G | 1 | a0002c0003t0003g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.504+2144G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163327 | ||||||
chr1:33163340
|
A | AT | 7 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 7 | HG04184.hp1 HG04199.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+2130dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163340 | ||||||
chr1:33163340
|
AT | A | 7 | a0002c0003t0003g0217a0002c0003t0003g0221a0002c0003t0003g0223others(4): Show | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.504+2130delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163340 | ||||||
chr1:33163361
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.504+2110G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163361 | ||||||
chr1:33163361
|
C | CT | 17 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(14): Show | 22 | HG00639.hp1 HG01243.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.504+2109dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163361 | ||||||
chr1:33163411
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.504+2060C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163411 | ||||||
chr1:33163435
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.504+2036T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163435 | ||||||
chr1:33163640
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(223): Show | 332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.504+1831A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163640 | ||||||
chr1:33163687
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.504+1784C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163687 | ||||||
chr1:33163697
|
C | T | 1 | a0002c0003t0003g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+1774G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33163697 | ||||||
chr1:33164039
|
A | T | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+1432T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164039 | ||||||
chr1:33164067
|
T | C | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.504+1404A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164067 | ||||||
chr1:33164068
|
C | A | 29 | a0001c0001t0002g0099a0001c0001t0002g0176a0001c0001t0002g0177others(26): Show | 62 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.504+1403G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164068 | ||||||
chr1:33164319
|
G | C | 1 | a0001c0012t0015g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.504+1152C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164319 | ||||||
chr1:33164382
|
A | G | 1 | a0001c0002t0002g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.504+1089T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164382 | ||||||
chr1:33164418
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.504+1053T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164418 | ||||||
chr1:33164553
|
A | G | 5 | a0001c0004t0003g0010a0001c0004t0003g0070a0001c0004t0003g0071others(2): Show | 7 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+918T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164553 | ||||||
chr1:33164585
|
C | CTGTT | 3 | a0001c0002t0002g0192a0001c0002t0002g0198a0001c0012t0015g0228 | 3 | HG01346.hp2 HG06807.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.504+882_504+885dup others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164585 | ||||||
chr1:33164613
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.504+858G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164613 | ||||||
chr1:33164651
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.504+820G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164651 | ||||||
chr1:33164695
|
A | G | 2 | a0001c0001t0003g0127a0001c0001t0003g0158 | 2 | HG03704.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.504+776T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164695 | ||||||
chr1:33164766
|
T | TATTCATT others(1): Show |
4 | a0001c0004t0003g0010a0001c0004t0003g0070a0001c0004t0003g0071others(1): Show | 6 | HG02109.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+697_504+704dup others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164766 | ||||||
chr1:33164766
|
T | TATTCATT others(5): Show |
1 | a0001c0006t0003g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.504+693_504+704dup others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164766 | ||||||
chr1:33164766
|
TATTCATT others(5): Show |
T | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.504+693_504+704del others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164766 | ||||||
chr1:33164790
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.504+681G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164790 | ||||||
chr1:33164807
|
A | G | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+664T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164807 | ||||||
chr1:33164939
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0125 | 2 | NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.504+532G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164939 | ||||||
chr1:33164955
|
AT | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(187): Show | 284 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.504+515delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33164955 | ||||||
chr1:33165045
|
G | T | 2 | a0001c0004t0003g0070a0001c0004t0003g0071 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.504+426C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165045 | ||||||
chr1:33165148
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0085 | 3 | HG01070.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.504+323G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165148 | ||||||
chr1:33165176
|
C | T | 1 | a0001c0001t0005g0171 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.504+295G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165176 | ||||||
chr1:33165333
|
T | TAGAA | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+137_504+138ins others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165333 | ||||||
chr1:33165403
|
T | C | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+68A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165403 | ||||||
chr1:33165443
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0002t0001g0180 | 3 | HG02572.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.504+28G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165443 | ||||||
chr1:33165459
|
G | A | 1 | a0001c0012t0015g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.504+12C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165459 | ||||||
chr1:33165468
|
C | A | 31 | a0001c0001t0001g0116a0001c0001t0002g0099a0001c0001t0002g0176others(28): Show | 64 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
splice_region_variant&intron_variant | LOW | c.504+3G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 2/4 | chr1 | 33165468 | ||||||
chr1:33165643
|
G | A | 1 | a0001c0007t0014g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.409-77C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165643 | ||||||
chr1:33165659
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.409-93C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165659 | ||||||
chr1:33165724
|
G | A | 1 | a0001c0001t0007g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.409-158C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165724 | ||||||
chr1:33165755
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0003g0086 | 6 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-189G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165755 | ||||||
chr1:33165874
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0085 | 3 | HG01070.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.409-308G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165874 | ||||||
chr1:33165952
|
G | A | 2 | a0001c0001t0006g0139a0001c0001t0006g0151 | 2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.409-386C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33165952 | ||||||
chr1:33166006
|
C | T | 5 | a0001c0001t0003g0127a0001c0001t0003g0148a0001c0001t0003g0158others(2): Show | 5 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.409-440G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166006 | ||||||
chr1:33166160
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(175): Show | 248 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.409-594T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166160 | ||||||
chr1:33166189
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.409-623C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166189 | ||||||
chr1:33166215
|
G | A | 7 | a0002c0003t0003g0217a0002c0003t0003g0221a0002c0003t0003g0223others(4): Show | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-649C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166215 | ||||||
chr1:33166304
|
G | T | 1 | a0001c0001t0003g0163 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.409-738C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166304 | ||||||
chr1:33166595
|
A | C | 1 | a0001c0004t0007g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.409-1029T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166595 | ||||||
chr1:33166898
|
G | A | 7 | a0002c0003t0003g0217a0002c0003t0003g0221a0002c0003t0003g0223others(4): Show | 12 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.409-1332C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166898 | ||||||
chr1:33166919
|
A | C | 1 | a0001c0001t0001g0032 | 2 | HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.409-1353T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166919 | ||||||
chr1:33166987
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.409-1421G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33166987 | ||||||
chr1:33167524
|
A | G | 48 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(45): Show | 86 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-1958T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167524 | ||||||
chr1:33167603
|
A | G | 1 | a0001c0001t0003g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.409-2037T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167603 | ||||||
chr1:33167875
|
T | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(8): Show | 12 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.409-2309A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167875 | ||||||
chr1:33167922
|
G | A | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | HG02886.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.409-2356C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33167922 | ||||||
chr1:33168081
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-2515T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168081 | ||||||
chr1:33168387
|
C | CT | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(146): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.409-2822dupA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168387 | ||||||
chr1:33168393
|
T | C | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-2827A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168393 | ||||||
chr1:33168458
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.409-2892G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168458 | ||||||
chr1:33168707
|
T | C | 3 | a0001c0002t0010g0232a0001c0002t0010g0233a0001c0002t0018g0231 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.409-3141A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168707 | ||||||
chr1:33168975
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.409-3409T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33168975 | ||||||
chr1:33169017
|
TC | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.409-3452delG | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169017 | ||||||
chr1:33169138
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.409-3572G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169138 | ||||||
chr1:33169162
|
C | G | 5 | a0001c0001t0007g0067a0001c0004t0003g0010a0001c0004t0003g0070others(2): Show | 7 | HG02109.hp2 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-3596G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169162 | ||||||
chr1:33169205
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-3639G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169205 | ||||||
chr1:33169236
|
C | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(11): Show | 15 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3670G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169236 | ||||||
chr1:33169260
|
T | G | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(227): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.409-3694A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169260 | ||||||
chr1:33169261
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.409-3695C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169261 | ||||||
chr1:33169423
|
G | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(11): Show | 15 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3857C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169423 | ||||||
chr1:33169424
|
G | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(11): Show | 15 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3858C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169424 | ||||||
chr1:33169530
|
C | T | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.409-3964G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169530 | ||||||
chr1:33169582
|
G | A | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-4016C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169582 | ||||||
chr1:33169602
|
G | A | 9 | a0001c0002t0001g0180a0001c0002t0003g0045a0002c0003t0003g0217others(6): Show | 15 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-4036C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169602 | ||||||
chr1:33169778
|
C | T | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-4212G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169778 | ||||||
chr1:33169783
|
A | G | 48 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(45): Show | 86 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.409-4217T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33169783 | ||||||
chr1:33170104
|
T | C | 4 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(1): Show | 4 | HG02080.hp2 HG03710.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-4538A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170104 | ||||||
chr1:33170158
|
C | T | 9 | a0001c0002t0001g0180a0001c0002t0003g0045a0002c0003t0003g0217others(6): Show | 15 | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.409-4592G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170158 | ||||||
chr1:33170187
|
A | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.409-4621T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170187 | ||||||
chr1:33170283
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-4717G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170283 | ||||||
chr1:33170321
|
TA | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(218): Show | 324 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.409-4756delT | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170321 | ||||||
chr1:33170425
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-4859A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170425 | ||||||
chr1:33170476
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.409-4910G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170476 | ||||||
chr1:33170793
|
T | C | 1 | a0001c0014t0002g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.409-5227A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170793 | ||||||
chr1:33170927
|
T | C | 8 | a0001c0001t0007g0067a0001c0002t0010g0232a0001c0002t0010g0233others(5): Show | 10 | HG01109.hp2 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.409-5361A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33170927 | ||||||
chr1:33171056
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.409-5490C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171056 | ||||||
chr1:33171136
|
C | T | 1 | a0001c0002t0002g0191 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.409-5570G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171136 | ||||||
chr1:33171309
|
T | G | 1 | a0001c0002t0003g0208 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.409-5743A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171309 | ||||||
chr1:33171575
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.409-6009G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171575 | ||||||
chr1:33171632
|
G | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.409-6066C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33171632 | ||||||
chr1:33172333
|
G | A | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-6767C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172333 | ||||||
chr1:33172378
|
C | T | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-6812G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172378 | ||||||
chr1:33172556
|
G | A | 5 | a0001c0001t0007g0067a0001c0004t0003g0010a0001c0004t0003g0070others(2): Show | 7 | HG02109.hp2 HG02559.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.409-6990C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172556 | ||||||
chr1:33172559
|
C | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(227): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.409-6993G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172559 | ||||||
chr1:33172602
|
G | A | 4 | a0001c0002t0003g0216a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.409-7036C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172602 | ||||||
chr1:33172824
|
C | T | 34 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0002t0002g0001others(31): Show | 71 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.409-7258G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172824 | ||||||
chr1:33172888
|
C | T | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.409-7322G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172888 | ||||||
chr1:33172982
|
A | T | 1 | a0001c0012t0015g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.409-7416T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33172982 | ||||||
chr1:33173059
|
A | C | 1 | a0001c0002t0002g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.409-7493T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173059 | ||||||
chr1:33173092
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.409-7526G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173092 | ||||||
chr1:33173135
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.409-7569G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173135 | ||||||
chr1:33173191
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0149 | 3 | HG02559.hp2 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.409-7625G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173191 | ||||||
chr1:33173192
|
C | T | 1 | a0001c0002t0003g0218 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.409-7626G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173192 | ||||||
chr1:33173596
|
C | G | 1 | a0001c0004t0003g0010 | 3 | HG02109.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.408+7429G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173596 | ||||||
chr1:33173678
|
CT | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(213): Show | 319 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.408+7346delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173678 | ||||||
chr1:33173754
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063 | 3 | HG01243.hp2 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.408+7271T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173754 | ||||||
chr1:33173918
|
C | T | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+7107G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33173918 | ||||||
chr1:33174089
|
A | G | 3 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0003g0211 | 3 | HG01069.hp2 HG01071.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.408+6936T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174089 | ||||||
chr1:33174231
|
T | G | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(229): Show | 339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.408+6794A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174231 | ||||||
chr1:33174371
|
A | G | 1 | a0002c0003t0003g0223 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.408+6654T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174371 | ||||||
chr1:33174404
|
G | A | 2 | a0001c0001t0006g0139a0001c0001t0006g0151 | 2 | NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.408+6621C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174404 | ||||||
chr1:33174558
|
A | C | 1 | a0001c0002t0003g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+6467T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174558 | ||||||
chr1:33174607
|
A | C | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+6418T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174607 | ||||||
chr1:33174893
|
ATG | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0014t0002g0183 | 3 | HG00733.hp1 HG03942.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.408+6130_408+6131d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174893 | ||||||
chr1:33174897
|
GTGTGTGT others(35): Show |
G | 1 | a0001c0001t0003g0159 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.408+6086_408+6127d others(44): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174897 | ||||||
chr1:33174903
|
G | GTA | 13 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0003g0037others(10): Show | 15 | HG00597.hp1 HG00673.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.408+6121_408+6122i others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174903 | ||||||
chr1:33174903
|
GTGTATAT others(43): Show |
G | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.408+6072_408+6121d others(52): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174903 | ||||||
chr1:33174903
|
GTGTATAT others(53): Show |
G | 1 | a0001c0001t0007g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.408+6062_408+6121d others(62): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174903 | ||||||
chr1:33174905
|
G | A | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(214): Show | 322 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.408+6120C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174905 | ||||||
chr1:33174905
|
G | GTA | 4 | a0001c0001t0003g0038a0001c0001t0003g0164a0001c0001t0003g0166others(1): Show | 5 | NA18953.hp1 NA18974.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6118_408+6119d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174905 | ||||||
chr1:33174920
|
C | T | 6 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0003g0211others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+6105G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174920 | ||||||
chr1:33174939
|
A | ATG | 4 | a0001c0001t0003g0158a0001c0004t0003g0070a0001c0004t0003g0071others(1): Show | 4 | HG02922.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6084_408+6085d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174939 | ||||||
chr1:33174939
|
A | ATGTG | 1 | a0001c0004t0003g0010 | 3 | HG02109.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.408+6082_408+6085d others(6): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174939 | ||||||
chr1:33174940
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.408+6085A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174940 | ||||||
chr1:33174945
|
G | GTATATAT others(3): Show |
6 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0164others(3): Show | 8 | NA18948.hp2 NA18953.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+6070_408+6079d others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174945
|
G | GTATATAT others(5): Show |
4 | a0001c0001t0003g0039a0001c0001t0003g0161a0001c0001t0003g0168others(1): Show | 5 | HG00673.hp1 NA19057.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+6068_408+6079d others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174945
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0003g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.408+6066_408+6079d others(16): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174945
|
GTA | G | 27 | a0001c0002t0002g0001a0001c0002t0002g0044a0001c0002t0002g0185others(24): Show | 59 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.408+6078_408+6079d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174945
|
GTATA | G | 6 | a0001c0002t0002g0043a0001c0002t0002g0184a0001c0002t0002g0189others(3): Show | 7 | HG02451.hp1 HG03490.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+6076_408+6079d others(6): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174945
|
GTATATA | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0129 | 4 | HG02976.hp2 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+6074_408+6079d others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174945
|
GTATATAT others(1): Show |
G | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(134): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.408+6072_408+6079d others(10): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174945
|
GTATATAT others(3): Show |
G | 1 | a0001c0001t0001g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.408+6070_408+6079d others(12): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174945 | ||||||
chr1:33174947
|
A | G | 16 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(13): Show | 21 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.408+6078T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174947 | ||||||
chr1:33174958
|
TATATATA others(9): Show |
T | 1 | a0001c0002t0003g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.408+6051_408+6066d others(18): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174958 | ||||||
chr1:33174962
|
T | C | 4 | a0001c0002t0003g0216a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6063A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174962 | ||||||
chr1:33174962
|
TATATATA others(1): Show |
T | 6 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0003g0211others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+6055_408+6062d others(10): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174962 | ||||||
chr1:33174964
|
TATATAC | T | 7 | a0001c0002t0001g0180a0001c0002t0003g0045a0002c0003t0003g0221others(4): Show | 13 | HG01891.hp2 HG02630.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.408+6055_408+6060d others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174964 | ||||||
chr1:33174968
|
T | C | 34 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0152others(31): Show | 74 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.408+6057A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174968 | ||||||
chr1:33174968
|
TAC | T | 3 | a0001c0002t0010g0232a0001c0002t0010g0233a0001c0002t0018g0231 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+6055_408+6056d others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174968 | ||||||
chr1:33174970
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(32): Show | 41 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.408+6055G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174970 | ||||||
chr1:33174971
|
A | G | 4 | a0001c0002t0003g0215a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6054T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174971 | ||||||
chr1:33174974
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.408+6051G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174974 | ||||||
chr1:33174976
|
T | C | 5 | a0001c0002t0003g0215a0001c0002t0003g0216a0001c0002t0003g0218others(2): Show | 5 | HG01243.hp1 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6049A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174976 | ||||||
chr1:33174978
|
T | C | 4 | a0001c0002t0003g0215a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6047A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174978 | ||||||
chr1:33174979
|
A | G | 1 | a0001c0002t0003g0216 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6046T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174979 | ||||||
chr1:33174980
|
C | T | 1 | a0001c0002t0003g0216 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6045G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174980 | ||||||
chr1:33174981
|
A | C | 1 | a0001c0001t0001g0023 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.408+6044T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174981 | ||||||
chr1:33174983
|
A | G | 4 | a0001c0002t0003g0215a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6042T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174983 | ||||||
chr1:33174983
|
A | T | 1 | a0001c0002t0003g0216 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6042T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174983 | ||||||
chr1:33174987
|
A | T | 4 | a0001c0002t0003g0215a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6038T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174987 | ||||||
chr1:33174989
|
G | A | 3 | a0001c0002t0003g0218a0001c0002t0003g0219a0001c0011t0001g0220 | 3 | HG02818.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.408+6036C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174989 | ||||||
chr1:33174990
|
C | T | 4 | a0001c0002t0003g0216a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6035G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174990 | ||||||
chr1:33174992
|
C | T | 4 | a0001c0002t0003g0216a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6033G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174992 | ||||||
chr1:33174993
|
A | G | 3 | a0001c0002t0003g0218a0001c0002t0003g0219a0001c0011t0001g0220 | 3 | HG02818.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.408+6032T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174993 | ||||||
chr1:33174994
|
C | T | 4 | a0001c0002t0003g0216a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG02818.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6031G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174994 | ||||||
chr1:33174995
|
A | G | 1 | a0001c0002t0003g0216 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+6030T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174995 | ||||||
chr1:33174996
|
C | T | 5 | a0001c0002t0003g0215a0001c0002t0003g0216a0001c0002t0003g0218others(2): Show | 5 | HG01243.hp1 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6029G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174996 | ||||||
chr1:33174998
|
C | T | 5 | a0001c0002t0003g0215a0001c0002t0003g0216a0001c0002t0003g0218others(2): Show | 5 | HG01243.hp1 HG02818.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+6027G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174998 | ||||||
chr1:33174999
|
A | G | 4 | a0001c0002t0003g0215a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6026T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33174999 | ||||||
chr1:33175001
|
G | A | 4 | a0001c0002t0003g0215a0001c0002t0003g0218a0001c0002t0003g0219others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+6024C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATATGT others(7): Show |
1 | a0001c0001t0001g0112 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.408+6023_408+6024i others(16): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATGTAT others(5): Show |
4 | a0001c0001t0001g0059a0001c0001t0001g0102a0001c0001t0001g0152others(1): Show | 4 | HG01109.hp2 HG02015.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+6012_408+6023d others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATGTAT others(11): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(5): Show | 10 | HG01891.hp1 HG01934.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+6006_408+6023d others(20): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATGTAT others(17): Show |
8 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0062others(5): Show | 10 | HG00639.hp2 HG01070.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+6000_408+6023d others(26): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATGTAT others(29): Show |
1 | a0001c0002t0009g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.408+6023_408+6024i others(38): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATTTA | 22 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(19): Show | 33 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(8): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATTTAT others(5): Show |
58 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(55): Show | 82 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATTTAT others(11): Show |
36 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 57 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(20): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATTTAT others(17): Show |
30 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0032others(27): Show | 37 | HG00099.hp2 HG00609.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(26): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATTTAT others(23): Show |
11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0131others(8): Show | 12 | HG00673.hp1 HG01123.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(32): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175001
|
G | GTATTTAT others(29): Show |
4 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0136others(1): Show | 4 | HG02257.hp1 NA18747.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+6023_408+6024i others(38): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175001 | ||||||
chr1:33175005
|
G | T | 9 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0001t0001g0113others(6): Show | 11 | HG02109.hp2 HG02559.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.408+6020C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175005 | ||||||
chr1:33175019
|
ATATGTAT others(5): Show |
A | 1 | a0001c0002t0003g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+5994_408+6005d others(14): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175019 | ||||||
chr1:33175031
|
T | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(187): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.408+5994A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175031 | ||||||
chr1:33175031
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.408+5994A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175031 | ||||||
chr1:33175049
|
A | ATATGTAT others(9): Show |
2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.408+5975_408+5976i others(18): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175049 | ||||||
chr1:33175051
|
T | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.408+5974A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175051 | ||||||
chr1:33175102
|
T | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.408+5923A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175102 | ||||||
chr1:33175141
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0077 | 3 | HG00438.hp2 HG02040.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.408+5884G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175141 | ||||||
chr1:33175206
|
AT | A | 54 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0035others(51): Show | 63 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.408+5818delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175206 | ||||||
chr1:33175232
|
AGAGATGG | A | 3 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0003g0211 | 3 | HG01069.hp2 HG01071.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.408+5786_408+5792d others(9): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175232 | ||||||
chr1:33175284
|
C | T | 1 | a0001c0001t0003g0066 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.408+5741G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175284 | ||||||
chr1:33175655
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(78): Show | 128 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.408+5370G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175655 | ||||||
chr1:33175682
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.408+5343C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175682 | ||||||
chr1:33175795
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.408+5230G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33175795 | ||||||
chr1:33176233
|
C | T | 1 | a0001c0002t0002g0187 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.408+4792G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176233 | ||||||
chr1:33176331
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(224): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.408+4694T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176331 | ||||||
chr1:33176346
|
C | T | 2 | a0001c0002t0003g0214a0001c0002t0003g0215 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.408+4679G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176346 | ||||||
chr1:33176533
|
G | C | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+4492C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176533 | ||||||
chr1:33176551
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.408+4474G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176551 | ||||||
chr1:33176711
|
G | A | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.408+4314C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176711 | ||||||
chr1:33176762
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0048 | 3 | HG02280.hp2 HG02451.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.408+4263G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176762 | ||||||
chr1:33176816
|
A | G | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | HG02886.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.408+4209T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176816 | ||||||
chr1:33176822
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.408+4203A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176822 | ||||||
chr1:33176989
|
A | G | 3 | a0001c0002t0010g0232a0001c0002t0010g0233a0001c0002t0018g0231 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+4036T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33176989 | ||||||
chr1:33177039
|
GCACACAC others(7): Show |
G | 1 | a0001c0001t0003g0169 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.408+3972_408+3985d others(16): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177039 | ||||||
chr1:33177050
|
C | CAT | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 225 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.408+3974_408+3975i others(4): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177050 | ||||||
chr1:33177051
|
G | A | 30 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(27): Show | 36 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.408+3974C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177051 | ||||||
chr1:33177052
|
C | T | 30 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(27): Show | 36 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.408+3973G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177052 | ||||||
chr1:33177053
|
A | G | 30 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(27): Show | 36 | HG00597.hp1 HG00673.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.408+3972T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177053 | ||||||
chr1:33177055
|
A | G | 18 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(15): Show | 21 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.408+3970T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177055 | ||||||
chr1:33177067
|
GCACA | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.408+3954_408+3957d others(6): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177067 | ||||||
chr1:33177090
|
A | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.408+3935T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177090 | ||||||
chr1:33177103
|
GCACACAC others(21): Show |
G | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.408+3894_408+3921d others(30): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177103 | ||||||
chr1:33177136
|
C | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(139): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.408+3889G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177136 | ||||||
chr1:33177187
|
C | T | 18 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0069others(15): Show | 21 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.408+3838G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177187 | ||||||
chr1:33177313
|
A | G | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+3712T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177313 | ||||||
chr1:33177348
|
A | T | 3 | a0001c0002t0010g0232a0001c0002t0010g0233a0001c0002t0018g0231 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+3677T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177348 | ||||||
chr1:33177440
|
G | A | 2 | a0001c0001t0003g0156a0001c0004t0007g0155 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.408+3585C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177440 | ||||||
chr1:33177760
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.408+3265T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177760 | ||||||
chr1:33177796
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.408+3229C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33177796 | ||||||
chr1:33178064
|
G | A | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | HG02886.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.408+2961C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178064 | ||||||
chr1:33178150
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.408+2875G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178150 | ||||||
chr1:33178198
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 6 | HG01069.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.408+2827G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178198 | ||||||
chr1:33178215
|
T | C | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+2810A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178215 | ||||||
chr1:33178382
|
C | T | 32 | a0001c0002t0002g0001a0001c0002t0002g0006a0001c0002t0002g0043others(29): Show | 69 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.408+2643G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178382 | ||||||
chr1:33178717
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | NA18962.hp2 NA19062.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.408+2308T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178717 | ||||||
chr1:33178751
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.408+2274T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178751 | ||||||
chr1:33178758
|
C | T | 1 | a0001c0002t0002g0186 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.408+2267G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178758 | ||||||
chr1:33178764
|
A | G | 2 | a0001c0002t0009g0181a0001c0002t0009g0182 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.408+2261T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178764 | ||||||
chr1:33178992
|
G | A | 13 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(10): Show | 16 | HG00597.hp1 HG00673.hp1 NA18948.hp2 others(13): Show |
intron_variant | MODIFIER | c.408+2033C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33178992 | ||||||
chr1:33179043
|
G | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.408+1982C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179043 | ||||||
chr1:33179197
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(224): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.408+1828T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179197 | ||||||
chr1:33179198
|
A | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(224): Show | 334 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.408+1827T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179198 | ||||||
chr1:33179231
|
G | A | 5 | a0002c0003t0003g0223a0002c0003t0003g0225a0002c0003t0004g0004others(2): Show | 10 | HG01891.hp2 HG02486.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+1794C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179231 | ||||||
chr1:33179572
|
G | A | 3 | a0001c0002t0009g0181a0001c0002t0009g0182a0001c0014t0002g0183 | 3 | HG02451.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.408+1453C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179572 | ||||||
chr1:33179688
|
G | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0170a0001c0001t0001g0173others(3): Show | 8 | NA18941.hp2 NA18948.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+1337C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179688 | ||||||
chr1:33179888
|
A | G | 3 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0003g0211 | 3 | HG01069.hp2 HG01071.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.408+1137T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179888 | ||||||
chr1:33179915
|
GT | G | 33 | a0001c0002t0002g0001a0001c0002t0002g0006a0001c0002t0002g0043others(30): Show | 70 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.408+1109delA | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179915 | ||||||
chr1:33179916
|
T | G | 2 | a0001c0002t0002g0184a0001c0002t0002g0185 | 2 | HG03834.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.408+1109A>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33179916 | ||||||
chr1:33180051
|
T | C | 3 | a0001c0002t0010g0232a0001c0002t0010g0233a0001c0002t0018g0231 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.408+974A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180051 | ||||||
chr1:33180060
|
GCT | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.408+963_408+964del others(2): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180060 | ||||||
chr1:33180064
|
A | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.408+961T>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180064 | ||||||
chr1:33180065
|
A | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.408+960T>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180065 | ||||||
chr1:33180117
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.408+908G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180117 | ||||||
chr1:33180209
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0051 | 3 | HG01255.hp1 HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.408+816T>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180209 | ||||||
chr1:33180370
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.408+655G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180370 | ||||||
chr1:33180498
|
C | T | 2 | a0001c0002t0003g0214a0001c0002t0003g0215 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.408+527G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180498 | ||||||
chr1:33180544
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(173): Show | 240 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.408+481C>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180544 | ||||||
chr1:33180589
|
C | G | 1 | a0001c0001t0002g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.408+436G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180589 | ||||||
chr1:33180648
|
T | C | 16 | a0001c0002t0001g0180a0001c0002t0003g0045a0001c0002t0003g0214others(13): Show | 22 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.408+377A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180648 | ||||||
chr1:33180651
|
C | T | 32 | a0001c0002t0002g0001a0001c0002t0002g0006a0001c0002t0002g0043others(29): Show | 69 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.408+374G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180651 | ||||||
chr1:33180751
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.408+274A>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180751 | ||||||
chr1:33180760
|
C | G | 1 | a0001c0002t0009g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.408+265G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180760 | ||||||
chr1:33180773
|
G | C | 1 | a0001c0006t0003g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.408+252C>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180773 | ||||||
chr1:33180818
|
A | AGGCCCCG others(23): Show |
3 | a0001c0002t0009g0181a0001c0002t0009g0182a0001c0014t0002g0183 | 3 | HG02451.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.408+177_408+206dup others(30): Show |
TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180818 | ||||||
chr1:33180836
|
C | A | 3 | a0001c0001t0001g0178a0001c0001t0002g0176a0001c0001t0002g0177 | 3 | HG02083.hp2 NA18967.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.408+189G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180836 | ||||||
chr1:33180896
|
T | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.408+129A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180896 | ||||||
chr1:33180899
|
C | A | 1 | a0001c0001t0001g0042 | 2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.408+126G>T | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180899 | ||||||
chr1:33180906
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 7 | HG02280.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+119G>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180906 | ||||||
chr1:33180953
|
T | C | 1 | a0001c0002t0002g0226 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.408+72A>G | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180953 | ||||||
chr1:33180967
|
G | T | 1 | a0001c0002t0001g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.408+58C>A | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33180967 | ||||||
chr1:33181013
|
C | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.408+12G>C | TRIM62 | ENSG00000116525.14 | transcript | ENST00000291416.10 | protein_coding | 1/4 | chr1 | 33181013 |