geneid | 57159 |
---|---|
ensemblid | ENSG00000138100.14 |
hgncid | 16008 |
symbol | TRIM54 |
name | tripartite motif containing 54 |
refseq_nuc | NM_187841.3 |
refseq_prot | NP_912730.2 |
ensembl_nuc | ENST00000380075.7 |
ensembl_prot | ENSP00000369415.3 |
mane_status | MANE Select |
chr | chr2 |
start | 27282429 |
end | 27307435 |
strand | + |
ver | v1.2 |
region | chr2:27282429-27307435 |
region5000 | chr2:27277429-27312435 |
regionname0 | TRIM54_chr2_27282429_27307435 |
regionname5000 | TRIM54_chr2_27277429_27312435 |
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 | 358 | 274 | 86 | 60 | 86 | 14 | 26 | 62 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0002 | 0/0 | 358 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0003 | 0/0 | 358 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
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 | 1/1 | 1077 | 267 | 81 | 58 | 86 | 14 | 26 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
c0002 | 0/0 | 1077 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
c0003 | 0/0 | 1077 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
c0004 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
c0005 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
c0006 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
c0007 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 853 | 267 | 80 | 58 | 85 | 14 | 28 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
t0002 | 0/0 | 853 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
t0003 | 0/0 | 853 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
t0004 | 0/0 | 853 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
t0005 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
t0006 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
t0007 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
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 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0024 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
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 | 1/1 | 1077 | 267 | 81 | 58 | 86 | 14 | 26 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0002 | 0/0 | 1077 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0003 | 0/0 | 1077 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0006 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0007 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0002c0005 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0003c0004 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1929 | 259 | 76 | 56 | 85 | 14 | 26 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0001t0002 | 0/0 | 1929 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0001t0003 | 0/0 | 1929 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0001t0004 | 0/0 | 1929 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0001t0006 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0001t0007 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0002t0001 | 0/0 | 1929 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0003t0001 | 0/0 | 1929 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0006t0001 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0001c0007t0005 | 0/0 | 1929 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0002c0005t0001 | 0/0 | 1929 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
a0003c0004t0001 | 0/0 | 1929 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | copy fasta | chr2 | 27277429 | 27312435 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0024 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0003t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0001c0007t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0002c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
a0003c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0020 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02602 | hp1 | a0003 | c0004 | t0001 | g0094 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02698 | hp1 | a0002 | c0005 | t0001 | g0150 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03041 | hp2 | a0001 | c0007 | t0005 | g0168 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03098 | hp2 | a0001 | c0006 | t0001 | g0038 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18988 | hp1 | a0001 | c0001 | t0007 | g0200 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ASW | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0024 | REF | REF | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0133 | REF | REF | TRIM54_chr2_27277429_27312435 | TRIM54 | chr2 | 27277429 | 27312435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27299361
|
G | A | 1 | a0002 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.458G>A | p.Gly153Asp | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/9 | 761/1930 | 458/1077 | 153/358 | chr2 | 27299361 | ||
chr2:27305007
|
G | T | 1 | a0003 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.562G>T | p.Val188Leu | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 4/9 | 865/1930 | 562/1077 | 188/358 | chr2 | 27305007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27282812
|
C | T | 1 | a0001c0007 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.81C>T | p.Pro27Pro | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 384/1930 | 81/1077 | 27/358 | chr2 | 27282812 | ||
chr2:27282869
|
G | A | 1 | a0003c0004 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.138G>A | p.Leu46Leu | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 441/1930 | 138/1077 | 46/358 | chr2 | 27282869 | ||
chr2:27282890
|
C | T | 1 | a0001c0003 | 2 | HG01256.hp2 HG01257.hp1 |
synonymous_variant | LOW | c.159C>T | p.Asp53Asp | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 462/1930 | 159/1077 | 53/358 | chr2 | 27282890 | ||
chr2:27304982
|
G | A | 1 | a0001c0002 | 3 | HG02559.hp1 HG02622.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.537G>A | p.Ala179Ala | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 4/9 | 840/1930 | 537/1077 | 179/358 | chr2 | 27304982 | ||
chr2:27305727
|
T | C | 1 | a0001c0006 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.753T>C | p.Arg251Arg | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 5/9 | 1056/1930 | 753/1077 | 251/358 | chr2 | 27305727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27282533
|
G | A | 1 | a0001c0001t0004 | 1 | HG01109.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | chr2 | 27282533 | ||||||
chr2:27282578
|
C | A | 1 | a0001c0001t0003 | 2 | HG01074.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-154C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/9 | 154 | chr2 | 27282578 | |||||
chr2:27306918
|
C | T | 1 | a0001c0001t0002 | 3 | HG02451.hp1 HG03209.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*33C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 377 | chr2 | 27306918 | |||||
chr2:27307002
|
T | C | 1 | a0001c0007t0005 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 461 | chr2 | 27307002 | |||||
chr2:27307066
|
C | T | 1 | a0001c0001t0004 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*181C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 525 | chr2 | 27307066 | |||||
chr2:27307159
|
C | T | 1 | a0001c0001t0007 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 618 | chr2 | 27307159 | |||||
chr2:27307298
|
C | G | 1 | a0001c0001t0006 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*413C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 9/9 | 757 | chr2 | 27307298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27282914
|
C | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0171others(71): Show | 77 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.168+15C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27282914 | ||||||
chr2:27283122
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0170 | 3 | NA18906.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.168+223C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283122 | ||||||
chr2:27283304
|
AAAAC | A | 4 | a0001c0001t0001g0028a0001c0002t0001g0025a0001c0002t0001g0026others(1): Show | 4 | HG02559.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+417_168+420del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283304 | |||||
chr2:27283349
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.168+450G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283349 | ||||||
chr2:27283543
|
T | C | 10 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.168+644T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283543 | ||||||
chr2:27283681
|
C | CT | 6 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0240others(3): Show | 6 | HG01934.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+795dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283681 | |||||
chr2:27283681
|
CT | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG02074.hp1 HG02486.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+795delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283681 | |||||
chr2:27283763
|
G | GGCACACA others(15): Show |
1 | a0001c0001t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+872_168+873ins others(22): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283763 | |||||
chr2:27283764
|
G | GCACACAC others(21): Show |
1 | a0001c0001t0001g0192 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(28): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | |||||
chr2:27283764
|
G | GCACACAC others(21): Show |
1 | a0001c0001t0001g0234 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(28): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | |||||
chr2:27283764
|
GCA | G | 3 | a0001c0001t0001g0028a0001c0001t0002g0163a0001c0001t0003g0166 | 3 | HG02451.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.168+879_168+880del others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | |||||
chr2:27283764
|
GCACACAC others(19): Show |
G | 3 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0170 | 4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+881_168+906del others(26): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283764 | |||||
chr2:27283766
|
A | ACACACGC others(9): Show |
1 | a0001c0001t0001g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | |||||
chr2:27283766
|
A | ACACACGC others(13): Show |
2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18966.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.168+872_168+873ins others(20): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | |||||
chr2:27283766
|
A | ACACACGC others(15): Show |
1 | a0001c0001t0001g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.168+872_168+873ins others(22): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | |||||
chr2:27283766
|
ACACACAC others(11): Show |
A | 1 | a0001c0002t0001g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+881_168+898del others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283766 | |||||
chr2:27283768
|
A | ACACGCAC others(9): Show |
1 | a0001c0001t0001g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.168+872_168+873ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | |||||
chr2:27283768
|
A | ACACGCAC others(11): Show |
3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00597.hp2 HG00738.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.168+872_168+873ins others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | |||||
chr2:27283768
|
A | ACACGCAC others(13): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG04199.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.168+872_168+873ins others(20): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | |||||
chr2:27283768
|
A | ACGCACGC others(11): Show |
1 | a0001c0001t0001g0237 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.168+870_168+871ins others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | |||||
chr2:27283768
|
A | ACGCACGC others(13): Show |
1 | a0001c0001t0001g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.168+870_168+871ins others(20): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283768 | |||||
chr2:27283770
|
A | ACGCACGC others(5): Show |
1 | a0001c0001t0001g0183 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.168+872_168+873ins others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | |||||
chr2:27283770
|
A | ACGCACGC others(7): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0185a0001c0001t0001g0186 | 5 | HG01074.hp2 HG01255.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+872_168+873ins others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | |||||
chr2:27283770
|
A | ACGCACGC others(9): Show |
7 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG02015.hp1 HG02015.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+872_168+873ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | |||||
chr2:27283770
|
A | ACGCACGC others(11): Show |
3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG01257.hp2 HG01258.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.168+872_168+873ins others(18): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | |||||
chr2:27283770
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG01496.hp2 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.168+871A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283770 | ||||||
chr2:27283770
|
ACACACAC others(7): Show |
A | 5 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 5 | HG00733.hp1 HG01167.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+881_168+894del others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283770 | |||||
chr2:27283772
|
A | G | 43 | a0001c0001t0001g0024a0001c0001t0001g0171a0001c0001t0001g0172others(40): Show | 44 | HG00735.hp1 HG00741.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.168+873A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283772 | ||||||
chr2:27283774
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0239 | 2 | HG00735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.168+875A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283774 | ||||||
chr2:27283776
|
A | G | 47 | a0001c0001t0001g0024a0001c0001t0001g0164a0001c0001t0001g0171others(44): Show | 48 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.168+877A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283776 | ||||||
chr2:27283778
|
A | ACG | 3 | a0001c0001t0001g0032a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | NA18747.hp1 NA18966.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168+885_168+886dup others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283778 | |||||
chr2:27283778
|
A | ACGCGCGC others(3): Show |
1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.168+886_168+887ins others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283778 | |||||
chr2:27283778
|
A | G | 47 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0171others(44): Show | 48 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.168+879A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283778 | ||||||
chr2:27283778
|
ACG | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0053others(7): Show | 17 | HG00639.hp2 HG00738.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+885_168+886del others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283778 | |||||
chr2:27283780
|
G | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0164a0001c0001t0001g0182others(28): Show | 33 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.168+881G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283780 | ||||||
chr2:27283782
|
G | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0164others(30): Show | 35 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.168+883G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283782 | ||||||
chr2:27283782
|
G | GCA | 7 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0039others(4): Show | 8 | HG01243.hp1 HG01884.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+884_168+885ins others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283782 | |||||
chr2:27283782
|
GCGCA | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01109.hp2 HG01346.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+885_168+888del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283782 | |||||
chr2:27283784
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(50): Show | 59 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.168+885G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283784 | ||||||
chr2:27283784
|
G | GCA | 30 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0015others(27): Show | 38 | HG00140.hp1 HG00558.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.168+921_168+922dup others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCACA | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 24 | HG00609.hp1 HG00733.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.168+919_168+922dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCACACA | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0074others(19): Show | 24 | HG00558.hp2 HG00735.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.168+917_168+922dup others(6): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCACACAC others(1): Show |
6 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0175others(3): Show | 6 | HG01192.hp2 HG01515.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+915_168+922dup others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCACACAC others(3): Show |
6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | HG01361.hp2 HG02165.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+913_168+922dup others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0187 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.168+911_168+922dup others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCACA | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0241others(1): Show | 4 | HG00323.hp1 HG02647.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+886_168+887ins others(6): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG00741.hp1 HG01516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+886_168+887ins others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCACAC others(3): Show |
6 | a0001c0001t0001g0173a0001c0001t0001g0216a0001c0001t0001g0217others(3): Show | 6 | HG02129.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+886_168+887ins others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCACAC others(5): Show |
3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0240 | 3 | HG01934.hp2 HG02630.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.168+886_168+887ins others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCACAC others(7): Show |
9 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0001t0001g0207others(6): Show | 9 | HG01123.hp2 HG01891.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+886_168+887ins others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCGCAC others(3): Show |
1 | a0001c0001t0001g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+886_168+887ins others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCGCAC others(7): Show |
3 | a0001c0001t0001g0174a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02486.hp2 HG02886.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.168+886_168+887ins others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCGCAC others(9): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0229a0001c0001t0001g0230 | 4 | HG01243.hp2 HG01346.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+886_168+887ins others(16): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
G | GCGCGCGC others(5): Show |
1 | a0001c0001t0001g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168+886_168+887ins others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
GCA | G | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0152others(5): Show | 8 | HG00609.hp2 HG00735.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+921_168+922del others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283784
|
GCACACAC others(3): Show |
G | 1 | a0001c0001t0001g0031 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.168+913_168+922del others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27283784 | |||||
chr2:27283786
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0206 | 2 | HG01934.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.168+887A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283786 | ||||||
chr2:27283788
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0181 | 2 | HG03831.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.168+889A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283788 | ||||||
chr2:27283790
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.168+891A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283790 | ||||||
chr2:27283800
|
A | G | 1 | a0001c0001t0006g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.168+901A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283800 | ||||||
chr2:27283821
|
C | CACACACA others(8): Show |
1 | a0001c0001t0001g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.168+922_168+923ins others(15): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283821 | ||||||
chr2:27283964
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0169 | 4 | HG00140.hp2 HG03195.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+1065C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283964 | ||||||
chr2:27283993
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0163 | 3 | HG02451.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.168+1094C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27283993 | ||||||
chr2:27284112
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062 | 7 | HG00738.hp2 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+1213G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284112 | ||||||
chr2:27284117
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.168+1218A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284117 | ||||||
chr2:27284290
|
A | C | 1 | a0001c0007t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+1391A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284290 | ||||||
chr2:27284387
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.168+1488C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284387 | ||||||
chr2:27284577
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.168+1678C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284577 | ||||||
chr2:27284704
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.168+1805G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27284704 | ||||||
chr2:27285280
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.168+2381A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285280 | ||||||
chr2:27285372
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(13): Show | 18 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+2473C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285372 | ||||||
chr2:27285588
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.168+2689T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285588 | ||||||
chr2:27285682
|
C | T | 1 | a0001c0007t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+2783C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285682 | ||||||
chr2:27285683
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0037others(15): Show | 22 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.168+2784G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285683 | ||||||
chr2:27285815
|
T | C | 16 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(13): Show | 18 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+2916T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285815 | ||||||
chr2:27285842
|
C | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0171others(71): Show | 77 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.168+2943C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27285842 | ||||||
chr2:27286115
|
T | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 8 | HG00438.hp2 HG00558.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+3216T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286115 | ||||||
chr2:27286164
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(127): Show | 146 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(143): Show |
intron_variant | MODIFIER | c.168+3265T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286164 | ||||||
chr2:27286165
|
AT | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0075others(2): Show | 6 | HG01074.hp1 HG03453.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+3279delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27286165 | |||||
chr2:27286190
|
A | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(13): Show | 18 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.168+3291A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286190 | ||||||
chr2:27286720
|
T | C | 1 | a0001c0007t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+3821T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27286720 | ||||||
chr2:27287026
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(6): Show | 12 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+4127G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287026 | ||||||
chr2:27287286
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0074 | 3 | HG02257.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.168+4387C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287286 | ||||||
chr2:27287444
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.168+4545G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287444 | ||||||
chr2:27287512
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.168+4613G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287512 | ||||||
chr2:27287527
|
A | AT | 21 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0017others(18): Show | 27 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+4638dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27287527 | |||||
chr2:27287649
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.168+4750G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287649 | ||||||
chr2:27287729
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.168+4830A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287729 | ||||||
chr2:27287765
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.168+4866G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287765 | ||||||
chr2:27287941
|
C | T | 1 | a0001c0001t0006g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.168+5042C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287941 | ||||||
chr2:27287959
|
C | G | 5 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG01891.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+5060C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287959 | ||||||
chr2:27287980
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.168+5081A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27287980 | ||||||
chr2:27288170
|
T | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.168+5271T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27288170 | ||||||
chr2:27288304
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 3 | NA18963.hp2 NA19057.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.168+5405C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27288304 | ||||||
chr2:27289232
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+6333G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289232 | ||||||
chr2:27289239
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.168+6340A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289239 | ||||||
chr2:27289563
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.168+6664C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289563 | ||||||
chr2:27289785
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.168+6886A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289785 | ||||||
chr2:27289860
|
C | CT | 38 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0050others(35): Show | 42 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.168+6990dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27289860 | |||||
chr2:27289860
|
CT | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0033others(12): Show | 17 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.168+6990delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27289860 | |||||
chr2:27289860
|
CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0028a0001c0001t0001g0164a0001c0001t0003g0165others(4): Show | 7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+6979_168+6990d others(14): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27289860 | |||||
chr2:27289862
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.168+6963T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289862 | ||||||
chr2:27289915
|
A | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0183a0001c0001t0001g0184others(8): Show | 13 | HG00597.hp2 HG01074.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+7016A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27289915 | ||||||
chr2:27290010
|
T | G | 74 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0171others(71): Show | 77 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.168+7111T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290010 | ||||||
chr2:27290199
|
A | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0061a0001c0001t0001g0062others(11): Show | 14 | HG00438.hp2 HG01074.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+7300A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290199 | ||||||
chr2:27290200
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0039others(4): Show | 8 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+7301T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290200 | ||||||
chr2:27290539
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.168+7640G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290539 | ||||||
chr2:27290550
|
G | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.168+7651G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290550 | ||||||
chr2:27290810
|
C | T | 1 | a0001c0003t0001g0020 | 2 | HG01256.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.169-7757C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290810 | ||||||
chr2:27290938
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169-7629C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27290938 | ||||||
chr2:27291056
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-7511A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291056 | ||||||
chr2:27291074
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.169-7493C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291074 | ||||||
chr2:27291248
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(88): Show | 96 | HG00597.hp2 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.169-7319A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291248 | ||||||
chr2:27291362
|
A | AAAAC | 3 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0074 | 3 | HG02257.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.169-7193_169-7190d others(6): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27291362 | |||||
chr2:27291448
|
GTT | G | 17 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-7114_169-7113d others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27291448 | |||||
chr2:27291471
|
C | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0164a0001c0001t0003g0165others(4): Show | 7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-7096C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291471 | ||||||
chr2:27291572
|
AAC | A | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-6991_169-6990d others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27291572 | |||||
chr2:27291589
|
T | G | 1 | a0001c0001t0004g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.169-6978T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291589 | ||||||
chr2:27291773
|
A | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(10): Show | 17 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.169-6794A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291773 | ||||||
chr2:27291886
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0004g0065 | 2 | HG01109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.169-6681C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291886 | ||||||
chr2:27291895
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0119 | 2 | NA18981.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.169-6672C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291895 | ||||||
chr2:27291904
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.169-6663G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291904 | ||||||
chr2:27291970
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-6597C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27291970 | ||||||
chr2:27292237
|
A | G | 74 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0171others(71): Show | 77 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.169-6330A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292237 | ||||||
chr2:27292262
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.169-6305A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292262 | ||||||
chr2:27292292
|
T | C | 17 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-6275T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292292 | ||||||
chr2:27292444
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0042others(8): Show | 14 | HG01884.hp1 HG01981.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-6123C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292444 | ||||||
chr2:27292491
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0132 | 2 | HG01516.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.169-6076G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292491 | ||||||
chr2:27292538
|
A | T | 1 | a0001c0001t0001g0010 | 2 | HG00558.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.169-6029A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292538 | ||||||
chr2:27292659
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 143 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(140): Show |
intron_variant | MODIFIER | c.169-5908C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292659 | ||||||
chr2:27292724
|
C | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-5843C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292724 | ||||||
chr2:27292869
|
C | G | 1 | a0001c0007t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-5698C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292869 | ||||||
chr2:27292980
|
C | T | 1 | a0001c0001t0001g0023 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.169-5587C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27292980 | ||||||
chr2:27293396
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.169-5171G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293396 | ||||||
chr2:27293422
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0147 | 2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.169-5145C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293422 | ||||||
chr2:27293477
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169-5090G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293477 | ||||||
chr2:27293888
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-4679T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293888 | ||||||
chr2:27293892
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.169-4675A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27293892 | ||||||
chr2:27294062
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.169-4505A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294062 | ||||||
chr2:27294163
|
C | CT | 3 | a0001c0001t0001g0118a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | NA18982.hp1 NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.169-4403dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27294163 | |||||
chr2:27294309
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.169-4258C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294309 | ||||||
chr2:27294579
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.169-3988G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294579 | ||||||
chr2:27294592
|
G | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0170 | 4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-3975G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294592 | ||||||
chr2:27294634
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062 | 7 | HG00738.hp2 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-3933G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294634 | ||||||
chr2:27294815
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(110): Show | 126 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(123): Show |
intron_variant | MODIFIER | c.169-3752A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294815 | ||||||
chr2:27294869
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.169-3698G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27294869 | ||||||
chr2:27294889
|
CA | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.169-3657delA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27294889 | |||||
chr2:27295122
|
A | G | 17 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-3445A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295122 | ||||||
chr2:27295127
|
G | A | 1 | a0001c0007t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169-3440G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295127 | ||||||
chr2:27295132
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.169-3435C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295132 | ||||||
chr2:27295453
|
G | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0147 | 2 | HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.169-3114G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295453 | ||||||
chr2:27295523
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.169-3044G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295523 | ||||||
chr2:27295596
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(4): Show | 8 | HG00733.hp1 HG01167.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-2971G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295596 | ||||||
chr2:27295641
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.169-2926C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27295641 | ||||||
chr2:27296007
|
G | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0207a0001c0001t0001g0220 | 3 | NA18955.hp2 NA18982.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.169-2560G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296007 | ||||||
chr2:27296236
|
G | A | 2 | a0001c0001t0002g0021a0001c0001t0002g0163 | 3 | HG02451.hp1 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.169-2331G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296236 | ||||||
chr2:27296264
|
A | G | 1 | a0003c0004t0001g0094 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.169-2303A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296264 | ||||||
chr2:27296285
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 143 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(140): Show |
intron_variant | MODIFIER | c.169-2282G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296285 | ||||||
chr2:27296386
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 143 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(140): Show |
intron_variant | MODIFIER | c.169-2181G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296386 | ||||||
chr2:27296522
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0159 | 2 | HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169-2045G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296522 | ||||||
chr2:27296588
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0002g0021a0001c0001t0002g0163 | 4 | HG02451.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1979C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296588 | ||||||
chr2:27296631
|
G | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0164a0001c0001t0003g0165others(4): Show | 7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-1936G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296631 | ||||||
chr2:27296722
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0154 | 2 | HG00280.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.169-1845C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27296722 | ||||||
chr2:27297052
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.169-1515C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297052 | ||||||
chr2:27297282
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.169-1285A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297282 | ||||||
chr2:27297388
|
C | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0027 | 3 | HG02559.hp1 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.169-1179C>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297388 | ||||||
chr2:27297834
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0170 | 4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-733A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297834 | ||||||
chr2:27297881
|
T | G | 1 | a0001c0002t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169-686T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27297881 | ||||||
chr2:27297980
|
C | CA | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0023others(46): Show | 55 | HG00639.hp2 HG00733.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.169-566dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | |||||
chr2:27297980
|
C | CAA | 8 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0051others(5): Show | 8 | HG01257.hp2 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-567_169-566dup others(2): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | |||||
chr2:27297980
|
C | CAAA | 55 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0037others(52): Show | 58 | HG00597.hp2 HG00738.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.169-568_169-566dup others(3): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | |||||
chr2:27297980
|
C | CAAAA | 7 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0216others(4): Show | 7 | HG00735.hp1 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-569_169-566dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 27297980 | |||||
chr2:27298002
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0227a0001c0001t0001g0228 | 4 | HG01257.hp2 HG01258.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-565G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298002 | ||||||
chr2:27298125
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.169-442A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298125 | ||||||
chr2:27298239
|
C | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.169-328C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298239 | ||||||
chr2:27298294
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.169-273A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298294 | ||||||
chr2:27298299
|
A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.169-268A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298299 | ||||||
chr2:27298361
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0132 | 2 | HG01516.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.169-206G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298361 | ||||||
chr2:27298395
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.169-172A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 1/8 | chr2 | 27298395 | ||||||
chr2:27298960
|
G | T | 1 | a0001c0002t0001g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.341+221G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 2/8 | chr2 | 27298960 | ||||||
chr2:27299166
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.342-79G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 2/8 | chr2 | 27299166 | ||||||
chr2:27299195
|
T | A | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.342-50T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 2/8 | chr2 | 27299195 | ||||||
chr2:27299675
|
C | CCTAT | 104 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(101): Show | 114 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.513+297_513+300dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | |||||
chr2:27299675
|
C | CCTATCTA others(1): Show |
31 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0034others(28): Show | 35 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.513+293_513+300dup others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | |||||
chr2:27299675
|
C | CCTATCTA others(5): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0201 | 2 | HG02109.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.513+289_513+300dup others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | |||||
chr2:27299675
|
CCTAT | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0037others(9): Show | 17 | HG00738.hp2 HG01243.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.513+297_513+300del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | |||||
chr2:27299675
|
CCTATCTA others(5): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.513+289_513+300del others(12): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299675 | |||||
chr2:27299884
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.513+468G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27299884 | ||||||
chr2:27299884
|
G | GT | 17 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+477dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27299884 | |||||
chr2:27299884
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.513+468G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27299884 | ||||||
chr2:27300221
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0110a0001c0001t0001g0114others(2): Show | 6 | HG00140.hp1 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+805G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300221 | ||||||
chr2:27300373
|
A | C | 1 | a0001c0001t0004g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.513+957A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300373 | ||||||
chr2:27300406
|
C | G | 17 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+990C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300406 | ||||||
chr2:27300451
|
C | T | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1035C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300451 | ||||||
chr2:27300550
|
C | CTACTAAT others(24): Show |
74 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0171others(71): Show | 77 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.513+1155_513+1156i others(33): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300550 | |||||
chr2:27300550
|
CTACTAAT others(24): Show |
C | 2 | a0001c0001t0001g0116a0001c0001t0001g0123 | 2 | HG01358.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.513+1177_513+1207d others(33): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300550 | |||||
chr2:27300568
|
A | ATTATTAG others(21): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0007t0005g0168 | 3 | HG03041.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.513+1155_513+1156i others(30): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300568 | |||||
chr2:27300568
|
A | ATTATTAG others(49): Show |
5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0162others(2): Show | 6 | HG00733.hp1 HG01167.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1155_513+1156i others(58): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27300568 | |||||
chr2:27300572
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(53): Show | 69 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.513+1156G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300572 | ||||||
chr2:27300616
|
T | C | 1 | a0001c0001t0007g0200 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.513+1200T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300616 | ||||||
chr2:27300814
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.513+1398C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27300814 | ||||||
chr2:27301135
|
C | CT | 21 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0028others(18): Show | 24 | HG01074.hp1 HG01884.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.513+1741dupT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27301135 | |||||
chr2:27301135
|
CT | C | 8 | a0001c0001t0001g0039a0001c0001t0001g0055a0001c0001t0001g0075others(5): Show | 8 | HG01169.hp2 HG01515.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+1741delT | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27301135 | |||||
chr2:27301225
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.513+1809C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301225 | ||||||
chr2:27301288
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+1872C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301288 | ||||||
chr2:27301617
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.513+2201C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301617 | ||||||
chr2:27301618
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.513+2202G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301618 | ||||||
chr2:27301642
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.513+2226C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301642 | ||||||
chr2:27301648
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.513+2232C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301648 | ||||||
chr2:27301660
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.513+2244C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27301660 | ||||||
chr2:27302108
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.513+2692T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302108 | ||||||
chr2:27302176
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(14): Show | 19 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.513+2760C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302176 | ||||||
chr2:27302246
|
C | T | 14 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0033others(11): Show | 15 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.514-2713C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302246 | ||||||
chr2:27302312
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0046others(7): Show | 11 | HG01884.hp1 HG01981.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.514-2647G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302312 | ||||||
chr2:27302395
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 130 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(127): Show |
intron_variant | MODIFIER | c.514-2564A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302395 | ||||||
chr2:27302415
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.514-2544C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302415 | ||||||
chr2:27302482
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(104): Show | 117 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.514-2477G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302482 | ||||||
chr2:27302566
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.514-2393C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302566 | ||||||
chr2:27302722
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.514-2237C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302722 | ||||||
chr2:27302756
|
A | C | 1 | a0001c0001t0002g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.514-2203A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302756 | ||||||
chr2:27302793
|
A | G | 83 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0028others(80): Show | 86 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.514-2166A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302793 | ||||||
chr2:27302915
|
G | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0162a0001c0001t0002g0021others(1): Show | 5 | HG02451.hp1 HG02922.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2044G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27302915 | ||||||
chr2:27303175
|
A | C | 1 | a0001c0001t0001g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.514-1784A>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303175 | ||||||
chr2:27303411
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.514-1548C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303411 | ||||||
chr2:27303547
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0054a0001c0001t0001g0057 | 3 | HG00639.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.514-1412C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303547 | ||||||
chr2:27303548
|
T | TA | 7 | a0001c0001t0001g0050a0001c0001t0001g0164a0001c0001t0003g0165others(4): Show | 7 | HG01074.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-1397dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27303548 | |||||
chr2:27303606
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.514-1353G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303606 | ||||||
chr2:27303760
|
A | G | 1 | a0001c0001t0001g0011 | 2 | NA18963.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.514-1199A>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303760 | ||||||
chr2:27303780
|
C | CA | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035 | 3 | HG00733.hp1 HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.514-1173dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27303780 | |||||
chr2:27303813
|
C | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0028others(68): Show | 74 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.514-1146C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303813 | ||||||
chr2:27303870
|
T | TA | 3 | a0001c0001t0001g0162a0001c0001t0002g0021a0001c0001t0002g0163 | 4 | HG02451.hp1 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1082dupA | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27303870 | |||||
chr2:27303922
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0001g0222 | 3 | HG03139.hp1 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.514-1037C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27303922 | ||||||
chr2:27304053
|
A | T | 1 | a0001c0001t0001g0009 | 2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.514-906A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304053 | ||||||
chr2:27304213
|
AATAT | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0170 | 4 | HG06807.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-736_514-733del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304213 | |||||
chr2:27304221
|
TATATAGA others(3): Show |
T | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.514-734_514-725del others(10): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304221 | |||||
chr2:27304223
|
T | TATAG | 11 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0046others(8): Show | 12 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.514-712_514-709dup others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | |||||
chr2:27304223
|
T | TATAGATA others(1): Show |
5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-716_514-709dup others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | |||||
chr2:27304223
|
TATAG | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0033others(14): Show | 21 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.514-712_514-709del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | |||||
chr2:27304223
|
TATAGATA others(1): Show |
T | 71 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0028others(68): Show | 74 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.514-716_514-709del others(8): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304223 | |||||
chr2:27304261
|
GATAT | G | 8 | a0001c0001t0001g0206a0001c0001t0001g0209a0001c0001t0001g0215others(5): Show | 8 | HG01934.hp1 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-684_514-681del others(4): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304261 | |||||
chr2:27304271
|
T | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0045others(2): Show | 5 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-688T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304271 | ||||||
chr2:27304275
|
T | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(115): Show | 132 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.514-684T>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304275 | ||||||
chr2:27304285
|
T | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0051others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-674T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304285 | ||||||
chr2:27304378
|
T | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(82): Show | 90 | HG00597.hp2 HG00733.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.514-581T>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304378 | ||||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0240 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(744): Show |
1 | a0001c0001t0001g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(751): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG00733.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0175 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0074 | 3 | HG02257.hp2 HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(742): Show |
4 | a0001c0001t0001g0109a0001c0001t0001g0151a0001c0001t0001g0153others(1): Show | 4 | HG01069.hp1 HG03669.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-563_514-562ins others(749): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(744): Show |
1 | a0001c0001t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(751): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304386
|
A | ACCAGCCT others(743): Show |
1 | a0001c0001t0001g0137 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.514-563_514-562ins others(750): Show |
TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 27304386 | |||||
chr2:27304413
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.514-546C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304413 | ||||||
chr2:27304424
|
A | T | 8 | a0001c0001t0001g0101a0001c0001t0001g0123a0001c0001t0001g0131others(5): Show | 8 | HG00323.hp2 HG00733.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-535A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304424 | ||||||
chr2:27304430
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.514-529A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304430 | ||||||
chr2:27304453
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(130): Show | 150 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(147): Show |
intron_variant | MODIFIER | c.514-506G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304453 | ||||||
chr2:27304465
|
T | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0078a0001c0001t0001g0092others(5): Show | 8 | HG00280.hp2 HG01069.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-494T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304465 | ||||||
chr2:27304518
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.514-441C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304518 | ||||||
chr2:27304666
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.514-293A>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304666 | ||||||
chr2:27304802
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0084 | 2 | HG02080.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.514-157G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304802 | ||||||
chr2:27304884
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.514-75G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304884 | ||||||
chr2:27304890
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 17 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.514-69C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304890 | ||||||
chr2:27304901
|
G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(12): Show | 17 | HG00733.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.514-58G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 3/8 | chr2 | 27304901 | ||||||
chr2:27305101
|
C | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(10): Show | 16 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.609+47C>G | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 4/8 | chr2 | 27305101 | ||||||
chr2:27305824
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(127): Show | 146 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(143): Show |
splice_region_variant&intron_variant | LOW | c.843+7T>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 5/8 | chr2 | 27305824 | ||||||
chr2:27306037
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.844-43G>A | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 5/8 | chr2 | 27306037 | ||||||
chr2:27306398
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0137 | 2 | HG01071.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.992-58C>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 7/8 | chr2 | 27306398 | ||||||
chr2:27306571
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*1+29G>T | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 8/8 | chr2 | 27306571 | ||||||
chr2:27306575
|
G | C | 1 | a0001c0001t0001g0015 | 2 | NA19070.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.*1+33G>C | TRIM54 | ENSG00000138100.14 | transcript | ENST00000380075.7 | protein_coding | 8/8 | chr2 | 27306575 |