geneid | 9866 |
---|---|
ensemblid | ENSG00000166436.18 |
hgncid | 29005 |
symbol | TRIM66 |
name | tripartite motif containing 66 |
refseq_nuc | NM_001388022.1 |
refseq_prot | NP_001374951.1 |
ensembl_nuc | ENST00000646038.2 |
ensembl_prot | ENSP00000495413.1 |
mane_status | MANE Select |
chr | chr11 |
start | 8612040 |
end | 8682665 |
strand | - |
ver | v1.2 |
region | chr11:8612040-8682665 |
region5000 | chr11:8607040-8687665 |
regionname0 | TRIM66_chr11_8612040_8682665 |
regionname5000 | TRIM66_chr11_8607040_8687665 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1392 | 125 | 37 | 21 | 44 | 5 | 17 | 37 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002 | 0/0 | 1392 | 78 | 2 | 15 | 48 | 6 | 7 | 39 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003 | 0/0 | 1392 | 60 | 14 | 10 | 32 | 1 | 3 | 25 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004 | 0/0 | 1392 | 41 | 0 | 11 | 23 | 2 | 5 | 20 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0005 | 0/0 | 1392 | 9 | 0 | 0 | 9 | 0 | 0 | 8 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0006 | 0/0 | 1392 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0007 | 0/0 | 1392 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0008 | 0/0 | 1392 | 7 | 1 | 2 | 0 | 2 | 2 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0009 | 0/0 | 1392 | 6 | 0 | 0 | 6 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0010 | 0/0 | 1392 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0011 | 0/0 | 1392 | 5 | 4 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0012 | 0/0 | 1392 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0013 | 0/0 | 1392 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0014 | 0/0 | 1392 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0015 | 0/0 | 1392 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0016 | 0/0 | 1392 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0017 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0018 | 0/0 | 1392 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0019 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0020 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0021 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0022 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0023 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0024 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0025 | 0/0 | 856 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0026 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0027 | 1/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0028 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0029 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0030 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 4179 | 123 | 37 | 20 | 44 | 5 | 16 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0002 | 0/0 | 4179 | 75 | 2 | 15 | 45 | 6 | 7 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0003 | 0/0 | 4179 | 58 | 14 | 10 | 30 | 1 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0004 | 0/0 | 4179 | 39 | 0 | 11 | 22 | 2 | 4 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0005 | 0/0 | 4179 | 9 | 0 | 0 | 9 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0006 | 0/0 | 4179 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0007 | 0/0 | 4179 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0008 | 0/0 | 4179 | 7 | 1 | 2 | 0 | 2 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0009 | 0/0 | 4179 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0010 | 0/0 | 4179 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0011 | 0/0 | 4179 | 5 | 4 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0012 | 0/0 | 4179 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0013 | 0/0 | 4179 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0014 | 0/0 | 4179 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0015 | 0/0 | 4179 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0016 | 0/0 | 4179 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0017 | 0/0 | 4179 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0018 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0019 | 0/0 | 4179 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0020 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0021 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0022 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0023 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0024 | 1/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0025 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0026 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0027 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0028 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0029 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0030 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0031 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0032 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0033 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0034 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0035 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0036 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0037 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
c0038 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 6517 | 117 | 32 | 21 | 48 | 4 | 11 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0002 | 0/0 | 6517 | 85 | 10 | 16 | 43 | 7 | 9 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0003 | 0/0 | 6517 | 51 | 6 | 5 | 38 | 1 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0004 | 0/0 | 6517 | 40 | 0 | 15 | 18 | 3 | 4 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0005 | 1/0 | 6517 | 10 | 7 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0006 | 0/0 | 6517 | 7 | 1 | 3 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0007 | 0/0 | 6517 | 7 | 1 | 2 | 0 | 2 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0008 | 0/0 | 6517 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0009 | 0/0 | 6517 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0010 | 0/0 | 6517 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0011 | 0/0 | 6517 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0012 | 0/0 | 6514 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0013 | 0/0 | 6521 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0014 | 0/0 | 6517 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0015 | 0/0 | 6517 | 3 | 1 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0016 | 0/0 | 6517 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0017 | 0/0 | 6517 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0018 | 0/0 | 6517 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0019 | 0/0 | 6517 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0020 | 0/0 | 6517 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0021 | 0/0 | 6517 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0022 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0023 | 0/0 | 6521 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0024 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0025 | 0/0 | 6517 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0026 | 0/0 | 6517 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0027 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0028 | 0/0 | 6517 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0029 | 0/0 | 6517 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0030 | 0/0 | 6517 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0031 | 0/0 | 6517 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0032 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0033 | 0/0 | 6517 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0034 | 0/0 | 6517 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0035 | 0/0 | 6517 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0036 | 0/0 | 6517 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0037 | 0/0 | 6517 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0038 | 0/0 | 6517 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0039 | 0/0 | 6517 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0040 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0041 | 0/0 | 6517 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0042 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0043 | 0/0 | 6517 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0044 | 0/0 | 6517 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0045 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0046 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
t0047 | 0/0 | 6517 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
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 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4179 | 123 | 37 | 20 | 44 | 5 | 16 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0023 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0026 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002 | 0/0 | 4179 | 75 | 2 | 15 | 45 | 6 | 7 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0019 | 0/0 | 4179 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0037 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0003 | 0/0 | 4179 | 58 | 14 | 10 | 30 | 1 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0030 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0031 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0004 | 0/0 | 4179 | 39 | 0 | 11 | 22 | 2 | 4 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0021 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0022 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0005c0005 | 0/0 | 4179 | 9 | 0 | 0 | 9 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0006c0006 | 0/0 | 4179 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0007c0007 | 0/0 | 4179 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0008c0008 | 0/0 | 4179 | 7 | 1 | 2 | 0 | 2 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0009c0009 | 0/0 | 4179 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0010c0010 | 0/0 | 4179 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0011c0011 | 0/0 | 4179 | 5 | 4 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0012c0012 | 0/0 | 4179 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0013c0013 | 0/0 | 4179 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0014c0015 | 0/0 | 4179 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0015c0014 | 0/0 | 4179 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0016c0016 | 0/0 | 4179 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0017c0018 | 0/0 | 4179 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0018c0017 | 0/0 | 4179 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0019c0020 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0020c0038 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0021c0035 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0022c0029 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0023c0033 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0024c0032 | 0/0 | 4179 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0025c0034 | 0/0 | 4189 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0026c0036 | 0/0 | 4179 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0027c0024 | 1/0 | 4179 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0028c0025 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0029c0027 | 0/0 | 4179 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0030c0028 | 0/0 | 4179 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10695 | 102 | 30 | 18 | 39 | 4 | 10 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0006 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0010 | 0/0 | 10695 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0015 | 0/0 | 10695 | 3 | 1 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0018 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0020 | 0/0 | 10695 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0022 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0034 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0035 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0037 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0040 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0041 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0042 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0001t0043 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0023t0004 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0001c0026t0001 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002t0002 | 0/0 | 10695 | 62 | 2 | 14 | 34 | 6 | 6 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002t0008 | 0/0 | 10695 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002t0014 | 0/0 | 10695 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002t0028 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002t0029 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002t0031 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0002t0044 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0019t0002 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0019t0030 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0002c0037t0002 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0003t0003 | 0/0 | 10695 | 42 | 6 | 5 | 29 | 1 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0003t0005 | 0/0 | 10695 | 9 | 7 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0003t0006 | 0/0 | 10695 | 6 | 1 | 3 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0003t0025 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0030t0003 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0003c0031t0003 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0004t0004 | 0/0 | 10695 | 34 | 0 | 11 | 18 | 2 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0004t0016 | 0/0 | 10695 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0004t0033 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0004t0036 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0021t0039 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0004c0022t0001 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0005c0005t0002 | 0/0 | 10695 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0005c0005t0013 | 0/0 | 10699 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0006c0006t0002 | 0/0 | 10695 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0007c0007t0003 | 0/0 | 10695 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0007c0007t0026 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0008c0008t0007 | 0/0 | 10695 | 7 | 1 | 2 | 0 | 2 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0009c0009t0001 | 0/0 | 10695 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0010c0010t0001 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0010c0010t0012 | 0/0 | 10692 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0011c0011t0004 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0011c0011t0021 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0011c0011t0027 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0011c0011t0045 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0012c0012t0009 | 0/0 | 10695 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0013c0013t0017 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0013c0013t0019 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0013c0013t0046 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0013c0013t0047 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0014c0015t0011 | 0/0 | 10695 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0015c0014t0004 | 0/0 | 10695 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0016c0016t0002 | 0/0 | 10695 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0017c0018t0023 | 0/0 | 10699 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0017c0018t0024 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0018c0017t0001 | 0/0 | 10695 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0019c0020t0003 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0020c0038t0001 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0021c0035t0002 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0022c0029t0009 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0023c0033t0032 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0024c0032t0002 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0025c0034t0002 | 0/0 | 10705 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0026c0036t0017 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0027c0024t0005 | 1/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0028c0025t0038 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0029c0027t0001 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
a0030c0028t0001 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | copy fasta | chr11 | 8607040 | 8687665 |
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 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0010g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0010g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0015g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0015g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0015g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0018g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0018g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0020g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0020g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0022g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0034g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0035g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0037g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0040g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0041g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0042g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0043g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0023t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0026t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0003 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0014g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0014g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0028g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0029g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0031g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0044g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0019t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0019t0030g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0037t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0025g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0030t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0031t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0004g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0016g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0016g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0016g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0033g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0036g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0021t0039g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0022t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0013g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0013g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0007t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0007t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0007t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0007t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0007t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0007t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0007t0026g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0008t0007g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0008t0007g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0008t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0008t0007g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0008t0007g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0012g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0012g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0011t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0011t0021g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0011t0021g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0011t0027g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0011t0045g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0012t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0012t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0012t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0012t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0012t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0013t0017g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0013t0019g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0013t0019g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0013t0046g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0013t0047g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0011g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0015c0014t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0015c0014t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0015c0014t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0015c0014t0004g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0016c0016t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0016c0016t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0016c0016t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0017c0018t0023g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0017c0018t0024g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0018c0017t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0018c0017t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0019c0020t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0020c0038t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0021c0035t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0022c0029t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0023c0033t0032g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0024c0032t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0025c0034t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0026c0036t0017g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0027c0024t0005g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0028c0025t0038g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0029c0027t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0030c0028t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0015 | c0014 | t0004 | g0305 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00099 | hp2 | a0008 | c0008 | t0007 | g0004 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00140 | hp2 | a0004 | c0004 | t0004 | g0337 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0279 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00323 | hp1 | a0008 | c0008 | t0007 | g0361 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00323 | hp2 | a0003 | c0003 | t0003 | g0114 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00408 | hp1 | a0002 | c0002 | t0029 | g0059 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00597 | hp1 | a0003 | c0003 | t0003 | g0161 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00597 | hp2 | a0005 | c0005 | t0013 | g0016 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00609 | hp1 | a0003 | c0003 | t0003 | g0184 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00609 | hp2 | a0028 | c0025 | t0038 | g0242 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00621 | hp1 | a0002 | c0019 | t0002 | g0237 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00621 | hp2 | a0009 | c0009 | t0001 | g0021 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00639 | hp1 | a0006 | c0006 | t0002 | g0207 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00642 | hp1 | a0004 | c0004 | t0004 | g0363 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00642 | hp2 | a0003 | c0003 | t0006 | g0185 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00735 | hp1 | a0003 | c0003 | t0003 | g0296 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00735 | hp2 | a0015 | c0014 | t0004 | g0311 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00738 | hp1 | a0004 | c0004 | t0004 | g0334 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00741 | hp1 | a0014 | c0015 | t0011 | g0075 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0349 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01071 | hp2 | a0004 | c0004 | t0004 | g0339 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01081 | hp1 | a0003 | c0003 | t0003 | g0358 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01099 | hp1 | a0015 | c0014 | t0004 | g0308 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0193 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01109 | hp2 | a0003 | c0003 | t0005 | g0209 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0282 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01167 | hp2 | a0001 | c0001 | t0035 | g0154 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01169 | hp1 | a0025 | c0034 | t0002 | g0350 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0277 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01192 | hp2 | a0004 | c0004 | t0004 | g0302 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01255 | hp2 | a0004 | c0004 | t0004 | g0366 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01256 | hp1 | a0004 | c0004 | t0004 | g0330 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01256 | hp2 | a0002 | c0002 | t0031 | g0283 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01257 | hp1 | a0003 | c0003 | t0003 | g0188 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01258 | hp1 | a0003 | c0003 | t0003 | g0187 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01258 | hp2 | a0004 | c0004 | t0004 | g0331 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01261 | hp1 | a0003 | c0003 | t0006 | g0190 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01261 | hp2 | a0004 | c0004 | t0004 | g0356 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01346 | hp1 | a0003 | c0003 | t0005 | g0208 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01358 | hp1 | a0004 | c0004 | t0004 | g0340 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0255 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01361 | hp2 | a0015 | c0014 | t0004 | g0364 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01433 | hp2 | a0004 | c0004 | t0004 | g0338 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01496 | hp1 | a0004 | c0004 | t0004 | g0020 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0276 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0029 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01516 | hp2 | a0001 | c0001 | t0034 | g0096 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0028 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01884 | hp2 | a0010 | c0010 | t0012 | g0007 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01891 | hp1 | a0006 | c0006 | t0002 | g0269 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01943 | hp2 | a0001 | c0001 | t0020 | g0085 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01952 | hp2 | a0008 | c0008 | t0007 | g0004 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01975 | hp1 | a0003 | c0003 | t0003 | g0359 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02015 | hp2 | a0009 | c0009 | t0001 | g0038 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02027 | hp1 | a0003 | c0003 | t0003 | g0235 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02027 | hp2 | a0030 | c0028 | t0001 | g0118 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02040 | hp2 | a0003 | c0003 | t0003 | g0160 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02055 | hp1 | a0010 | c0010 | t0001 | g0137 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02055 | hp2 | a0008 | c0008 | t0007 | g0321 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02056 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02056 | hp2 | a0004 | c0004 | t0004 | g0300 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02071 | hp1 | a0003 | c0003 | t0003 | g0232 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0290 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02074 | hp2 | a0004 | c0004 | t0004 | g0303 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02083 | hp1 | a0004 | c0004 | t0004 | g0309 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02132 | hp2 | a0009 | c0009 | t0001 | g0132 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02145 | hp1 | a0006 | c0006 | t0002 | g0250 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02145 | hp2 | a0026 | c0036 | t0017 | g0367 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02148 | hp1 | a0018 | c0017 | t0001 | g0026 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02165 | hp1 | a0003 | c0003 | t0003 | g0241 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02258 | hp1 | a0003 | c0003 | t0003 | g0112 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02258 | hp2 | a0022 | c0029 | t0009 | g0206 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02273 | hp1 | a0018 | c0017 | t0001 | g0025 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02273 | hp2 | a0029 | c0027 | t0001 | g0095 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02293 | hp1 | a0001 | c0023 | t0004 | g0319 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02293 | hp2 | a0008 | c0008 | t0007 | g0004 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02451 | hp2 | a0014 | c0015 | t0011 | g0078 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02523 | hp2 | a0002 | c0002 | t0008 | g0123 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02572 | hp1 | a0017 | c0018 | t0024 | g0030 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02572 | hp2 | a0003 | c0003 | t0003 | g0048 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02615 | hp1 | a0013 | c0013 | t0019 | g0121 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02615 | hp2 | a0003 | c0003 | t0003 | g0074 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02622 | hp2 | a0006 | c0006 | t0002 | g0047 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0248 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02683 | hp2 | a0001 | c0001 | t0015 | g0229 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02717 | hp1 | a0017 | c0018 | t0023 | g0119 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02717 | hp2 | a0001 | c0001 | t0040 | g0022 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02723 | hp1 | a0006 | c0006 | t0002 | g0239 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0167 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0268 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02809 | hp1 | a0003 | c0003 | t0003 | g0129 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02818 | hp1 | a0001 | c0001 | t0042 | g0092 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02818 | hp2 | a0001 | c0001 | t0022 | g0018 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02886 | hp2 | a0012 | c0012 | t0009 | g0214 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02895 | hp1 | a0013 | c0013 | t0017 | g0130 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02895 | hp2 | a0012 | c0012 | t0009 | g0227 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02896 | hp1 | a0003 | c0003 | t0005 | g0009 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02896 | hp2 | a0013 | c0013 | t0046 | g0052 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02897 | hp1 | a0003 | c0003 | t0005 | g0009 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02897 | hp2 | a0012 | c0012 | t0009 | g0228 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02922 | hp1 | a0003 | c0003 | t0005 | g0151 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02970 | hp1 | a0011 | c0011 | t0021 | g0051 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02970 | hp2 | a0003 | c0003 | t0005 | g0211 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0035 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02976 | hp2 | a0001 | c0001 | t0020 | g0086 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03017 | hp1 | a0004 | c0004 | t0033 | g0355 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03017 | hp2 | a0001 | c0001 | t0037 | g0352 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03098 | hp1 | a0011 | c0011 | t0027 | g0218 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03098 | hp2 | a0010 | c0010 | t0012 | g0056 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03130 | hp2 | a0011 | c0011 | t0021 | g0050 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03139 | hp1 | a0014 | c0015 | t0011 | g0077 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03139 | hp2 | a0010 | c0010 | t0012 | g0007 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03195 | hp2 | a0003 | c0003 | t0005 | g0210 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03209 | hp1 | a0023 | c0033 | t0032 | g0107 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03209 | hp2 | a0013 | c0013 | t0019 | g0120 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03225 | hp1 | a0010 | c0010 | t0012 | g0093 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03225 | hp2 | a0011 | c0011 | t0045 | g0053 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03491 | hp1 | a0002 | c0002 | t0044 | g0292 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03516 | hp1 | a0014 | c0015 | t0011 | g0076 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03516 | hp2 | a0006 | c0006 | t0002 | g0240 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03540 | hp2 | a0003 | c0003 | t0003 | g0073 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03654 | hp2 | a0004 | c0004 | t0004 | g0328 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03669 | hp2 | a0016 | c0016 | t0002 | g0346 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0323 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03688 | hp2 | a0001 | c0001 | t0015 | g0215 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03704 | hp1 | a0004 | c0004 | t0004 | g0304 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03704 | hp2 | a0001 | c0026 | t0001 | g0031 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03710 | hp1 | a0016 | c0016 | t0002 | g0347 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0115 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03831 | hp1 | a0008 | c0008 | t0007 | g0365 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03831 | hp2 | a0001 | c0001 | t0043 | g0094 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03834 | hp1 | a0004 | c0004 | t0004 | g0106 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03927 | hp1 | a0016 | c0016 | t0002 | g0348 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03927 | hp2 | a0001 | c0001 | t0041 | g0084 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03942 | hp2 | a0008 | c0008 | t0007 | g0197 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04184 | hp1 | a0003 | c0003 | t0006 | g0192 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04184 | hp2 | a0004 | c0021 | t0039 | g0318 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04199 | hp1 | a0011 | c0011 | t0004 | g0274 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04204 | hp1 | a0003 | c0003 | t0006 | g0191 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18906 | hp1 | a0003 | c0003 | t0003 | g0113 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18940 | hp2 | a0003 | c0003 | t0003 | g0147 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18944 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18944 | hp2 | a0004 | c0004 | t0004 | g0336 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18950 | hp1 | a0003 | c0003 | t0003 | g0183 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18951 | hp1 | a0009 | c0009 | t0001 | g0046 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18953 | hp1 | a0007 | c0007 | t0003 | g0175 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0360 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18954 | hp1 | a0002 | c0002 | t0014 | g0286 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18956 | hp1 | a0002 | c0002 | t0008 | g0155 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18956 | hp2 | a0004 | c0004 | t0004 | g0307 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18957 | hp1 | a0003 | c0003 | t0025 | g0180 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18959 | hp1 | a0004 | c0004 | t0004 | g0315 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0061 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18961 | hp1 | a0002 | c0037 | t0002 | g0271 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18961 | hp2 | a0003 | c0003 | t0003 | g0055 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18962 | hp2 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18963 | hp1 | a0003 | c0003 | t0003 | g0357 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18963 | hp2 | a0005 | c0005 | t0002 | g0262 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18964 | hp1 | a0002 | c0002 | t0008 | g0157 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18966 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18973 | hp1 | a0004 | c0004 | t0036 | g0327 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18973 | hp2 | a0003 | c0003 | t0003 | g0177 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18975 | hp1 | a0002 | c0002 | t0014 | g0287 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18975 | hp2 | a0002 | c0002 | t0028 | g0164 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18978 | hp1 | a0007 | c0007 | t0003 | g0173 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18980 | hp2 | a0004 | c0004 | t0004 | g0301 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18981 | hp1 | a0001 | c0001 | t0010 | g0045 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18981 | hp2 | a0005 | c0005 | t0002 | g0261 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18984 | hp1 | a0003 | c0003 | t0003 | g0362 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18984 | hp2 | a0004 | c0004 | t0004 | g0329 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18989 | hp2 | a0001 | c0001 | t0010 | g0042 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18991 | hp1 | a0009 | c0009 | t0001 | g0043 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18991 | hp2 | a0005 | c0005 | t0002 | g0251 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18992 | hp1 | a0003 | c0003 | t0003 | g0153 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18992 | hp2 | a0002 | c0002 | t0008 | g0126 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18994 | hp2 | a0004 | c0004 | t0004 | g0333 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18998 | hp1 | a0001 | c0001 | t0010 | g0040 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18999 | hp2 | a0004 | c0004 | t0004 | g0332 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19000 | hp2 | a0002 | c0002 | t0008 | g0165 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19003 | hp1 | a0003 | c0003 | t0003 | g0071 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19004 | hp1 | a0004 | c0004 | t0004 | g0312 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19005 | hp1 | a0005 | c0005 | t0002 | g0267 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19005 | hp2 | a0004 | c0004 | t0016 | g0313 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19006 | hp2 | a0003 | c0030 | t0003 | g0181 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19007 | hp1 | a0005 | c0005 | t0002 | g0266 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19007 | hp2 | a0007 | c0007 | t0003 | g0174 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19010 | hp1 | a0002 | c0002 | t0014 | g0293 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19011 | hp1 | a0004 | c0004 | t0004 | g0335 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19011 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19012 | hp1 | a0003 | c0031 | t0003 | g0179 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19012 | hp2 | a0005 | c0005 | t0013 | g0016 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19030 | hp1 | a0006 | c0006 | t0002 | g0249 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19054 | hp1 | a0002 | c0002 | t0008 | g0204 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19054 | hp2 | a0004 | c0004 | t0016 | g0317 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19055 | hp1 | a0007 | c0007 | t0003 | g0176 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19056 | hp1 | a0004 | c0004 | t0004 | g0345 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19056 | hp2 | a0003 | c0003 | t0003 | g0178 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19058 | hp1 | a0020 | c0038 | t0001 | g0068 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19058 | hp2 | a0002 | c0019 | t0030 | g0368 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19060 | hp1 | a0007 | c0007 | t0026 | g0169 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19063 | hp1 | a0003 | c0003 | t0003 | g0284 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19064 | hp2 | a0004 | c0004 | t0004 | g0172 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19065 | hp1 | a0009 | c0009 | t0001 | g0037 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19066 | hp1 | a0001 | c0001 | t0010 | g0039 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19067 | hp2 | a0003 | c0003 | t0003 | g0057 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19068 | hp1 | a0001 | c0001 | t0010 | g0041 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19068 | hp2 | a0003 | c0003 | t0003 | g0146 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19074 | hp1 | a0004 | c0004 | t0004 | g0306 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19077 | hp1 | a0004 | c0004 | t0004 | g0314 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19077 | hp2 | a0019 | c0020 | t0003 | g0194 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19079 | hp1 | a0004 | c0004 | t0004 | g0310 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0182 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19080 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19081 | hp1 | a0021 | c0035 | t0002 | g0252 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19081 | hp2 | a0004 | c0004 | t0004 | g0316 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19084 | hp2 | a0007 | c0007 | t0003 | g0064 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19085 | hp1 | a0003 | c0003 | t0003 | g0216 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19088 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19089 | hp1 | a0005 | c0005 | t0002 | g0263 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19089 | hp2 | a0004 | c0022 | t0001 | g0344 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19090 | hp1 | a0007 | c0007 | t0003 | g0063 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19091 | hp1 | a0005 | c0005 | t0013 | g0291 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20129 | hp2 | a0003 | c0003 | t0005 | g0195 | AFR | ASW | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20752 | hp1 | a0024 | c0032 | t0002 | g0171 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0003 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20805 | hp1 | a0004 | c0004 | t0004 | g0351 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0278 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01123 | hp1 | a0003 | c0003 | t0006 | g0186 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02486 | hp2 | a0012 | c0012 | t0009 | g0212 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02559 | hp1 | a0013 | c0013 | t0047 | g0054 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02559 | hp2 | a0012 | c0012 | t0009 | g0213 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03471 | hp1 | a0001 | c0001 | t0018 | g0034 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03471 | hp2 | a0010 | c0010 | t0001 | g0140 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG06807 | hp1 | a0003 | c0003 | t0006 | g0170 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18955 | hp1 | a0004 | c0004 | t0016 | g0322 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20300 | hp1 | a0003 | c0003 | t0005 | g0152 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20300 | hp2 | a0006 | c0006 | t0002 | g0036 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA21309 | hp1 | a0006 | c0006 | t0002 | g0275 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA21309 | hp2 | a0001 | c0001 | t0015 | g0354 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0189 | REF | REF | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
homoSapiens_grch38 | hp1 | a0027 | c0024 | t0005 | g0127 | REF | REF | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8618903
|
C | G | 1 | a0016 | 3 | HG03669.hp2 HG03710.hp1 HG03927.hp1 |
missense_variant | MODERATE | c.3966G>C | p.Glu1322Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/25 | 4578/10695 | 3966/4179 | 1322/1392 | chr11 | 8618903 | ||
chr11:8619490
|
T | C | 2 | a0015a0029 | 5 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(2): Show |
missense_variant | MODERATE | c.3793A>G | p.Ile1265Val | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/25 | 4405/10695 | 3793/4179 | 1265/1392 | chr11 | 8619490 | ||
chr11:8624530
|
G | C | 1 | a0026 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2848C>G | p.Arg950Gly | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/25 | 3460/10695 | 2848/4179 | 950/1392 | chr11 | 8624530 | ||
chr11:8624811
|
G | T | 1 | a0006 | 9 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(6): Show |
missense_variant | MODERATE | c.2728C>A | p.Gln910Lys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3340/10695 | 2728/4179 | 910/1392 | chr11 | 8624811 | ||
chr11:8624903
|
T | G | 1 | a0005 | 9 | HG00597.hp2 NA18963.hp2 NA18981.hp2 others(6): Show |
missense_variant | MODERATE | c.2636A>C | p.Gln879Pro | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3248/10695 | 2636/4179 | 879/1392 | chr11 | 8624903 | ||
chr11:8624990
|
C | T | 3 | a0012a0022a0023 | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
missense_variant | MODERATE | c.2549G>A | p.Ser850Asn | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3161/10695 | 2549/4179 | 850/1392 | chr11 | 8624990 | ||
chr11:8625020
|
A | AGGCTGGG others(3): Show |
1 | a0025 | 1 | HG01169.hp1 | frameshift_variant | HIGH | c.2509_2518dupATGCCC others(4): Show |
p.Leu840fs | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3130/10695 | 2518/4179 | 840/1392 | chr11 | 8625020 | ||
chr11:8625123
|
T | G | 10 | a0002a0005a0006others(7): Show | 109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
missense_variant | MODERATE | c.2416A>C | p.Asn806His | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3028/10695 | 2416/4179 | 806/1392 | chr11 | 8625123 | ||
chr11:8625216
|
G | C | 12 | a0002a0005a0006others(9): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
missense_variant | MODERATE | c.2323C>G | p.Leu775Val | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 2935/10695 | 2323/4179 | 775/1392 | chr11 | 8625216 | ||
chr11:8640416
|
C | T | 1 | a0019 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.1959G>A | p.Met653Ile | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2571/10695 | 1959/4179 | 653/1392 | chr11 | 8640416 | ||
chr11:8640543
|
T | C | 22 | a0001a0002a0004others(19): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
missense_variant | MODERATE | c.1832A>G | p.His611Arg | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2444/10695 | 1832/4179 | 611/1392 | chr11 | 8640543 | ||
chr11:8640738
|
C | T | 1 | a0022 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1637G>A | p.Arg546Gln | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2249/10695 | 1637/4179 | 546/1392 | chr11 | 8640738 | ||
chr11:8640763
|
C | T | 1 | a0018 | 2 | HG02148.hp1 HG02273.hp1 |
missense_variant | MODERATE | c.1612G>A | p.Val538Met | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2224/10695 | 1612/4179 | 538/1392 | chr11 | 8640763 | ||
chr11:8640906
|
T | A | 1 | a0030 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.1469A>T | p.His490Leu | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2081/10695 | 1469/4179 | 490/1392 | chr11 | 8640906 | ||
chr11:8640948
|
G | A | 1 | a0021 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1427C>T | p.Ser476Phe | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2039/10695 | 1427/4179 | 476/1392 | chr11 | 8640948 | ||
chr11:8640969
|
T | C | 12 | a0001a0004a0009others(9): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
missense_variant | MODERATE | c.1406A>G | p.His469Arg | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2018/10695 | 1406/4179 | 469/1392 | chr11 | 8640969 | ||
chr11:8641102
|
A | G | 1 | a0008 | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
missense_variant | MODERATE | c.1273T>C | p.Tyr425His | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 1885/10695 | 1273/4179 | 425/1392 | chr11 | 8641102 | ||
chr11:8645796
|
A | G | 1 | a0010 | 6 | HG01884.hp2 HG02055.hp1 HG03098.hp2 others(3): Show |
missense_variant | MODERATE | c.1049T>C | p.Ile350Thr | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/25 | 1661/10695 | 1049/4179 | 350/1392 | chr11 | 8645796 | ||
chr11:8646469
|
T | G | 1 | a0014 | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.935A>C | p.Asn312Thr | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/25 | 1547/10695 | 935/4179 | 312/1392 | chr11 | 8646469 | ||
chr11:8646535
|
C | T | 1 | a0008 | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
missense_variant | MODERATE | c.869G>A | p.Arg290Lys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/25 | 1481/10695 | 869/4179 | 290/1392 | chr11 | 8646535 | ||
chr11:8648461
|
A | C | 1 | a0018 | 2 | HG02148.hp1 HG02273.hp1 |
missense_variant | MODERATE | c.680T>G | p.Met227Arg | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/25 | 1292/10695 | 680/4179 | 227/1392 | chr11 | 8648461 | ||
chr11:8671858
|
G | A | 19 | a0002a0003a0005others(16): Show | 201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
missense_variant | MODERATE | c.268C>T | p.Arg90Cys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 880/10695 | 268/4179 | 90/1392 | chr11 | 8671858 | ||
chr11:8671858
|
G | T | 2 | a0004a0015 | 45 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(42): Show |
missense_variant | MODERATE | c.268C>A | p.Arg90Ser | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 880/10695 | 268/4179 | 90/1392 | chr11 | 8671858 | ||
chr11:8671891
|
C | A | 1 | a0020 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.235G>T | p.Gly79Cys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 847/10695 | 235/4179 | 79/1392 | chr11 | 8671891 | ||
chr11:8672022
|
C | T | 2 | a0007a0019 | 8 | NA18953.hp1 NA18978.hp1 NA19007.hp2 others(5): Show |
missense_variant | MODERATE | c.104G>A | p.Gly35Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 716/10695 | 104/4179 | 35/1392 | chr11 | 8672022 | ||
chr11:8672028
|
C | T | 1 | a0009 | 6 | HG00621.hp2 HG02015.hp2 HG02132.hp2 others(3): Show |
missense_variant | MODERATE | c.98G>A | p.Gly33Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 710/10695 | 98/4179 | 33/1392 | chr11 | 8672028 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8624731
|
C | G | 1 | a0003c0031 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.2808G>C | p.Leu936Leu | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3420/10695 | 2808/4179 | 936/1392 | chr11 | 8624731 | ||
chr11:8624782
|
A | C | 1 | a0001c0026 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.2757T>G | p.Ser919Ser | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3369/10695 | 2757/4179 | 919/1392 | chr11 | 8624782 | ||
chr11:8625058
|
G | A | 3 | a0012c0012a0022c0029a0023c0033 | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
synonymous_variant | LOW | c.2481C>T | p.Ser827Ser | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3093/10695 | 2481/4179 | 827/1392 | chr11 | 8625058 | ||
chr11:8625112
|
A | T | 1 | a0003c0030 | 1 | NA19006.hp2 | synonymous_variant | LOW | c.2427T>A | p.Ala809Ala | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3039/10695 | 2427/4179 | 809/1392 | chr11 | 8625112 | ||
chr11:8640578
|
C | T | 1 | a0004c0021 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1797G>A | p.Gln599Gln | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2409/10695 | 1797/4179 | 599/1392 | chr11 | 8640578 | ||
chr11:8648532
|
G | A | 1 | a0002c0019 | 2 | HG00621.hp1 NA19058.hp2 |
synonymous_variant | LOW | c.609C>T | p.Pro203Pro | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/25 | 1221/10695 | 609/4179 | 203/1392 | chr11 | 8648532 | ||
chr11:8649822
|
C | T | 4 | a0001c0023a0004c0004a0004c0021others(1): Show | 45 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(42): Show |
synonymous_variant | LOW | c.510G>A | p.Leu170Leu | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/25 | 1122/10695 | 510/4179 | 170/1392 | chr11 | 8649822 | ||
chr11:8671850
|
G | A | 1 | a0002c0037 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.276C>T | p.Asp92Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 888/10695 | 276/4179 | 92/1392 | chr11 | 8671850 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8612045
|
A | G | 2 | a0013c0013t0019a0013c0013t0047 | 3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5899T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5899 | chr11 | 8612045 | |||||
chr11:8612081
|
A | G | 1 | a0002c0002t0029 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5863T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5863 | chr11 | 8612081 | |||||
chr11:8612141
|
G | A | 1 | a0001c0001t0020 | 2 | HG01943.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5803C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5803 | chr11 | 8612141 | |||||
chr11:8612734
|
C | T | 1 | a0001c0001t0037 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5210G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5210 | chr11 | 8612734 | |||||
chr11:8612735
|
G | A | 1 | a0002c0019t0030 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5209C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5209 | chr11 | 8612735 | |||||
chr11:8612741
|
TATC | T | 1 | a0010c0010t0012 | 4 | HG01884.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5200_*5202delGAT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5200 | chr11 | 8612741 | |||||
chr11:8612861
|
G | A | 1 | a0002c0002t0008 | 6 | HG02523.hp2 NA18956.hp1 NA18964.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5083C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5083 | chr11 | 8612861 | |||||
chr11:8612971
|
C | A | 3 | a0013c0013t0017a0013c0013t0046a0026c0036t0017 | 3 | HG02145.hp2 HG02895.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4973G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4973 | chr11 | 8612971 | |||||
chr11:8613116
|
G | C | 2 | a0003c0003t0025a0004c0004t0036 | 2 | NA18957.hp1 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4828C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4828 | chr11 | 8613116 | |||||
chr11:8613595
|
T | C | 3 | a0012c0012t0009a0022c0029t0009a0023c0033t0032 | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4349A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4349 | chr11 | 8613595 | |||||
chr11:8613649
|
T | A | 2 | a0001c0001t0006a0003c0003t0006 | 7 | HG00642.hp2 HG01123.hp1 HG01261.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4295A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4295 | chr11 | 8613649 | |||||
chr11:8613929
|
T | A | 1 | a0004c0021t0039 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4015A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4015 | chr11 | 8613929 | |||||
chr11:8613948
|
G | A | 1 | a0028c0025t0038 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3996C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3996 | chr11 | 8613948 | |||||
chr11:8614350
|
A | AAAAT | 2 | a0005c0005t0013a0017c0018t0023 | 4 | HG00597.hp2 HG02717.hp1 NA19012.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3590_*3593dupATTT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3593 | chr11 | 8614350 | |||||
chr11:8614350
|
A | T | 10 | a0001c0023t0004a0004c0004t0004a0004c0004t0016others(7): Show | 52 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3594T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3594 | chr11 | 8614350 | |||||
chr11:8614558
|
T | C | 37 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(34): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*3386A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3386 | chr11 | 8614558 | |||||
chr11:8614581
|
T | C | 3 | a0012c0012t0009a0022c0029t0009a0023c0033t0032 | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3363A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3363 | chr11 | 8614581 | |||||
chr11:8614609
|
T | A | 53 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(50): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*3335A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3335 | chr11 | 8614609 | |||||
chr11:8614758
|
G | A | 1 | a0004c0021t0039 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3186C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3186 | chr11 | 8614758 | |||||
chr11:8614792
|
G | C | 34 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(31): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*3152C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3152 | chr11 | 8614792 | |||||
chr11:8614796
|
A | C | 72 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(69): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*3148T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3148 | chr11 | 8614796 | |||||
chr11:8614803
|
A | G | 53 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(50): Show | 300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*3141T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3141 | chr11 | 8614803 | |||||
chr11:8614861
|
T | C | 3 | a0012c0012t0009a0022c0029t0009a0023c0033t0032 | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3083A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3083 | chr11 | 8614861 | |||||
chr11:8614951
|
C | T | 1 | a0001c0001t0035 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2993G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2993 | chr11 | 8614951 | |||||
chr11:8615398
|
C | A | 1 | a0001c0001t0040 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2546G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2546 | chr11 | 8615398 | |||||
chr11:8615506
|
C | A | 1 | a0001c0001t0041 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2438G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2438 | chr11 | 8615506 | |||||
chr11:8615644
|
G | C | 52 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(49): Show | 299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*2300C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2300 | chr11 | 8615644 | |||||
chr11:8615675
|
T | C | 1 | a0001c0001t0042 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2269 | chr11 | 8615675 | |||||
chr11:8615745
|
G | A | 2 | a0017c0018t0023a0017c0018t0024 | 2 | HG02572.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2199C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2199 | chr11 | 8615745 | |||||
chr11:8615990
|
G | C | 1 | a0001c0001t0043 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1954 | chr11 | 8615990 | |||||
chr11:8615998
|
T | C | 3 | a0012c0012t0009a0022c0029t0009a0023c0033t0032 | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1946A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1946 | chr11 | 8615998 | |||||
chr11:8616265
|
A | G | 1 | a0001c0001t0034 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1679T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1679 | chr11 | 8616265 | |||||
chr11:8616311
|
T | C | 1 | a0002c0002t0031 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1633A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1633 | chr11 | 8616311 | |||||
chr11:8616379
|
G | C | 52 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(49): Show | 299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*1565C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1565 | chr11 | 8616379 | |||||
chr11:8616702
|
C | T | 1 | a0004c0004t0033 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1242G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1242 | chr11 | 8616702 | |||||
chr11:8616726
|
C | A | 1 | a0001c0001t0010 | 5 | NA18981.hp1 NA18989.hp2 NA18998.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1218G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1218 | chr11 | 8616726 | |||||
chr11:8616819
|
C | T | 1 | a0011c0011t0021 | 2 | HG02970.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1125G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1125 | chr11 | 8616819 | |||||
chr11:8617283
|
C | G | 1 | a0011c0011t0027 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 661 | chr11 | 8617283 | |||||
chr11:8617566
|
G | A | 1 | a0001c0001t0015 | 3 | HG02683.hp2 HG03688.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*378C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 378 | chr11 | 8617566 | |||||
chr11:8617653
|
T | C | 35 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(32): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*291A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 291 | chr11 | 8617653 | |||||
chr11:8617778
|
G | A | 32 | a0001c0001t0001a0001c0001t0010a0001c0001t0015others(29): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*166C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 166 | chr11 | 8617778 | |||||
chr11:8617784
|
C | T | 9 | a0001c0001t0006a0003c0003t0003a0003c0003t0006others(6): Show | 60 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*160G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 160 | chr11 | 8617784 | |||||
chr11:8672321
|
A | G | 2 | a0017c0018t0023a0017c0018t0024 | 2 | HG02572.hp1 HG02717.hp1 |
5_prime_UTR_variant | MODIFIER | c.-47T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 5/25 | 47 | chr11 | 8672321 | |||||
chr11:8672349
|
G | A | 1 | a0004c0004t0016 | 3 | NA18955.hp1 NA19005.hp2 NA19054.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-75C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 5/25 | chr11 | 8672349 | ||||||
chr11:8674836
|
T | C | 1 | a0002c0002t0044 | 1 | HG03491.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/25 | 2562 | chr11 | 8674836 | |||||
chr11:8680060
|
T | A | 4 | a0011c0011t0021a0011c0011t0045a0013c0013t0046others(1): Show | 5 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-544A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 2/25 | 7786 | chr11 | 8680060 | |||||
chr11:8682619
|
C | G | 1 | a0001c0001t0022 | 1 | HG02818.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-566G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/25 | chr11 | 8682619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8618119
|
G | A | 1 | a0004c0004t0004g0338 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4120-116C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618119 | ||||||
chr11:8618447
|
G | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(177): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.4119+303C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618447 | ||||||
chr11:8618521
|
C | G | 1 | a0002c0002t0002g0163 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4119+229G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618521 | ||||||
chr11:8618526
|
GCA | G | 4 | a0001c0001t0018g0034a0001c0001t0018g0035a0017c0018t0023g0119others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.4119+222_4119+223d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618526 | ||||||
chr11:8618662
|
C | T | 2 | a0001c0001t0010g0041a0001c0001t0010g0045 | 2 | NA18981.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4119+88G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618662 | ||||||
chr11:8619191
|
C | G | 1 | a0001c0001t0022g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3900+192G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/24 | chr11 | 8619191 | ||||||
chr11:8619223
|
G | T | 1 | a0026c0036t0017g0367 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3900+160C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/24 | chr11 | 8619223 | ||||||
chr11:8619349
|
G | A | 13 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029others(10): Show | 13 | HG00408.hp1 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.3900+34C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/24 | chr11 | 8619349 | ||||||
chr11:8619555
|
G | A | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3748-20C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619555 | ||||||
chr11:8619767
|
G | C | 3 | a0004c0004t0004g0332a0004c0004t0004g0333a0004c0004t0004g0345 | 3 | NA18994.hp2 NA18999.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3748-232C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619767 | ||||||
chr11:8619935
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3747+115T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619935 | ||||||
chr11:8619954
|
C | A | 359 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(356): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.3747+96G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619954 | ||||||
chr11:8620028
|
A | G | 3 | a0004c0004t0016g0313a0004c0004t0016g0317a0004c0004t0016g0322 | 3 | NA18955.hp1 NA19005.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.3747+22T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8620028 | ||||||
chr11:8620036
|
G | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3747+14C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8620036 | ||||||
chr11:8620192
|
T | G | 39 | a0002c0002t0028g0164a0003c0003t0003g0002a0003c0003t0003g0005others(36): Show | 43 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.3673-68A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 21/24 | chr11 | 8620192 | ||||||
chr11:8620335
|
G | A | 359 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(356): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.3672+111C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 21/24 | chr11 | 8620335 | ||||||
chr11:8620342
|
T | C | 2 | a0001c0001t0001g0103a0029c0027t0001g0095 | 2 | HG01175.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.3672+104A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 21/24 | chr11 | 8620342 | ||||||
chr11:8620671
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(183): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.3546-99G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 20/24 | chr11 | 8620671 | ||||||
chr11:8620782
|
T | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG00140.hp1 HG01243.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.3546-210A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 20/24 | chr11 | 8620782 | ||||||
chr11:8621478
|
C | A | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3256-157G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 19/24 | chr11 | 8621478 | ||||||
chr11:8621504
|
C | CAGCAGGG others(32): Show |
1 | a0003c0030t0003g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3255+102_3255+140d others(41): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 19/24 | chr11 | 8621504 | ||||||
chr11:8621909
|
T | A | 1 | a0003c0030t0003g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3081-90A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8621909 | ||||||
chr11:8621980
|
C | A | 13 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0065others(10): Show | 15 | NA18946.hp1 NA18950.hp2 NA18966.hp2 others(12): Show |
intron_variant | MODIFIER | c.3081-161G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8621980 | ||||||
chr11:8622048
|
A | C | 1 | a0001c0001t0043g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3081-229T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622048 | ||||||
chr11:8622255
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3081-436G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622255 | ||||||
chr11:8622280
|
CATATATA others(5): Show |
C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3081-473_3081-462d others(14): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622280 | ||||||
chr11:8622296
|
T | C | 1 | a0001c0001t0001g0289 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3081-477A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622296 | ||||||
chr11:8622321
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+495C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622321 | ||||||
chr11:8622336
|
CACA | C | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+477_3080+479d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622336 | ||||||
chr11:8622339
|
AACACAC | A | 6 | a0003c0003t0003g0216a0003c0030t0003g0181a0011c0011t0021g0050others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3080+471_3080+476d others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622339 | ||||||
chr11:8622339
|
AACACACA others(1): Show |
A | 59 | a0003c0003t0003g0002a0003c0003t0003g0005a0003c0003t0003g0048others(56): Show | 63 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.3080+469_3080+476d others(10): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622339 | ||||||
chr11:8622346
|
AC | A | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+469delG | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622346 | ||||||
chr11:8622357
|
CACACACA others(3): Show |
C | 1 | a0022c0029t0009g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3080+449_3080+458d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622357 | ||||||
chr11:8622365
|
C | CACACACA others(37): Show |
1 | a0013c0013t0019g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(45): Show |
1 | a0004c0021t0039g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(54): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(49): Show |
1 | a0004c0004t0004g0329 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(58): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(53): Show |
1 | a0004c0004t0004g0336 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(62): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
1 | a0011c0011t0004g0274 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(31): Show |
1 | a0004c0004t0004g0328 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(33): Show |
1 | a0013c0013t0047g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(37): Show |
5 | a0004c0004t0004g0301a0004c0004t0004g0306a0004c0004t0004g0315others(2): Show | 5 | HG03209.hp2 NA18959.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(45): Show |
2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(54): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(47): Show |
1 | a0001c0001t0001g0024 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(56): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(49): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0223 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(58): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(23): Show |
1 | a0001c0001t0001g0245 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
1 | a0001c0001t0001g0326 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(29): Show |
1 | a0001c0001t0001g0325 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(33): Show |
1 | a0009c0009t0001g0043 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(35): Show |
4 | a0015c0014t0004g0305a0015c0014t0004g0308a0015c0014t0004g0311others(1): Show | 4 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(37): Show |
1 | a0004c0004t0004g0304 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(41): Show |
1 | a0001c0001t0040g0022 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(43): Show |
1 | a0001c0001t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(47): Show |
1 | a0004c0004t0004g0333 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(56): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(25): Show |
1 | a0001c0001t0010g0039 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
3 | a0001c0001t0001g0044a0001c0001t0010g0041a0001c0026t0001g0031 | 3 | HG03704.hp2 NA19068.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(29): Show |
1 | a0001c0001t0001g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(33): Show |
1 | a0001c0001t0001g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(35): Show |
3 | a0001c0001t0001g0128a0001c0023t0004g0319a0004c0004t0004g0312 | 3 | HG02293.hp1 NA19004.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(37): Show |
3 | a0001c0001t0001g0066a0004c0004t0004g0302a0004c0004t0004g0351 | 3 | HG00639.hp2 HG01192.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(39): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0032 | 3 | HG03486.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(41): Show |
1 | a0001c0001t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(45): Show |
1 | a0004c0004t0004g0345 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(54): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(47): Show |
1 | a0004c0004t0004g0332 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(56): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(51): Show |
1 | a0001c0001t0001g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(60): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(9): Show |
1 | a0004c0004t0004g0337 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(18): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(19): Show |
1 | a0001c0001t0001g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(23): Show |
1 | a0001c0001t0010g0040 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(25): Show |
4 | a0001c0001t0001g0289a0001c0001t0010g0045a0009c0009t0001g0021others(1): Show | 4 | HG00621.hp2 HG02132.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
2 | a0001c0001t0010g0042a0001c0001t0015g0354 | 2 | NA18989.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(29): Show |
3 | a0001c0001t0001g0117a0009c0009t0001g0038a0009c0009t0001g0046 | 3 | HG02015.hp2 NA18951.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(31): Show |
3 | a0004c0004t0016g0313a0004c0004t0036g0327a0018c0017t0001g0025 | 3 | HG02273.hp1 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(33): Show |
3 | a0001c0001t0001g0058a0004c0004t0004g0309a0004c0004t0004g0335 | 3 | HG02083.hp1 HG02257.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(35): Show |
10 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0111others(7): Show | 10 | HG00642.hp1 HG01071.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(37): Show |
3 | a0004c0004t0004g0106a0004c0004t0004g0307a0004c0004t0004g0366 | 3 | HG01255.hp2 HG03834.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(39): Show |
1 | a0004c0004t0033g0355 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(41): Show |
1 | a0001c0001t0001g0083 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(43): Show |
1 | a0001c0001t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(21): Show |
2 | a0001c0001t0001g0294a0001c0001t0037g0352 | 2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(23): Show |
1 | a0004c0022t0001g0344 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(25): Show |
4 | a0001c0001t0001g0138a0001c0001t0001g0224a0001c0001t0001g0243others(1): Show | 4 | HG01496.hp2 HG01884.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
3 | a0001c0001t0001g0142a0004c0004t0004g0310a0010c0010t0001g0140 | 3 | HG00280.hp1 HG03471.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(29): Show |
2 | a0018c0017t0001g0026a0030c0028t0001g0118 | 2 | HG02027.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(31): Show |
6 | a0001c0001t0001g0108a0001c0001t0015g0229a0004c0004t0004g0020others(3): Show | 7 | HG01261.hp2 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(33): Show |
10 | a0001c0001t0001g0109a0001c0001t0001g0133a0001c0001t0001g0201others(7): Show | 10 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(35): Show |
1 | a0004c0004t0004g0300 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(37): Show |
2 | a0001c0001t0001g0067a0004c0004t0004g0340 | 2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(39): Show |
1 | a0001c0001t0041g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(41): Show |
1 | a0001c0001t0001g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(43): Show |
1 | a0001c0001t0001g0225 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(11): Show |
1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(20): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(17): Show |
1 | a0001c0001t0001g0090 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(19): Show |
2 | a0001c0001t0034g0096a0004c0004t0004g0172 | 2 | HG01516.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(21): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0166others(4): Show | 9 | HG00609.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(23): Show |
4 | a0001c0001t0001g0079a0001c0001t0001g0100a0001c0001t0001g0143others(1): Show | 4 | HG01070.hp1 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(25): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0149 | 2 | HG02015.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
3 | a0001c0001t0001g0098a0001c0001t0001g0198a0001c0001t0042g0092 | 3 | HG01081.hp2 HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(29): Show |
5 | a0001c0001t0001g0089a0001c0001t0001g0134a0001c0001t0001g0168others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(31): Show |
5 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0246others(2): Show | 5 | HG02040.hp1 HG02074.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(33): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0236 | 2 | HG03490.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(35): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0189a0001c0001t0001g0233 | 3 | NA19070.hp2 NA19240.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(39): Show |
1 | a0001c0001t0001g0220 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(11): Show |
1 | a0001c0001t0001g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(20): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(17): Show |
1 | a0001c0001t0001g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(19): Show |
5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 5 | HG01175.hp1 HG02273.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(21): Show |
5 | a0001c0001t0001g0244a0001c0001t0001g0295a0001c0001t0001g0341others(2): Show | 5 | HG01167.hp2 NA18946.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(23): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0343others(1): Show | 5 | HG02080.hp1 HG02155.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(25): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0104 | 2 | HG02074.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0091a0001c0001t0001g0105others(3): Show | 7 | HG02698.hp1 HG03486.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(29): Show |
2 | a0001c0001t0001g0139a0010c0010t0012g0056 | 2 | HG03098.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(31): Show |
1 | a0001c0001t0022g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(43): Show |
1 | a0001c0001t0001g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(17): Show |
1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(25): Show |
1 | a0001c0001t0001g0299 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(27): Show |
1 | a0001c0001t0001g0298 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(29): Show |
1 | a0001c0001t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACACA others(31): Show |
2 | a0001c0001t0001g0297a0001c0001t0018g0034 | 2 | HG03471.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CACACATA others(29): Show |
1 | a0001c0001t0018g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | CAT | 8 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0193others(5): Show | 11 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.3080+449_3080+450d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622365
|
C | T | 11 | a0003c0003t0003g0216a0003c0030t0003g0181a0006c0006t0002g0240others(8): Show | 11 | HG02145.hp1 HG02895.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.3080+451G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | ||||||
chr11:8622367
|
T | C | 10 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(7): Show | 12 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.3080+449A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622367 | ||||||
chr11:8622369
|
T | C | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+447A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622369 | ||||||
chr11:8622424
|
C | T | 1 | a0004c0004t0036g0327 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3080+392G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622424 | ||||||
chr11:8622442
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(292): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.3080+374A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622442 | ||||||
chr11:8622633
|
G | T | 1 | a0003c0030t0003g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3080+183C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622633 | ||||||
chr11:8622637
|
C | G | 1 | a0003c0030t0003g0181 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3080+179G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622637 | ||||||
chr11:8622704
|
C | T | 1 | a0003c0003t0003g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3080+112G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622704 | ||||||
chr11:8622983
|
T | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(182): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.3020-107A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8622983 | ||||||
chr11:8623015
|
TCATA | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(182): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.3020-143_3020-140d others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623015 | ||||||
chr11:8623052
|
T | C | 1 | a0020c0038t0001g0068 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3020-176A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623052 | ||||||
chr11:8623053
|
C | T | 1 | a0004c0004t0033g0355 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3020-177G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623053 | ||||||
chr11:8623443
|
A | G | 1 | a0002c0002t0008g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3020-567T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623443 | ||||||
chr11:8623447
|
A | G | 2 | a0013c0013t0017g0130a0013c0013t0046g0052 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3020-571T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623447 | ||||||
chr11:8623534
|
A | C | 1 | a0001c0001t0042g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3020-658T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623534 | ||||||
chr11:8623558
|
G | A | 1 | a0001c0001t0043g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3020-682C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623558 | ||||||
chr11:8623685
|
C | G | 1 | a0001c0001t0010g0045 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3019+674G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623685 | ||||||
chr11:8623854
|
T | A | 4 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019+505A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623854 | ||||||
chr11:8623862
|
T | C | 1 | a0022c0029t0009g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3019+497A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623862 | ||||||
chr11:8623908
|
G | A | 1 | a0001c0001t0043g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3019+451C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623908 | ||||||
chr11:8623917
|
C | A | 2 | a0003c0003t0003g0112a0003c0003t0003g0113 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3019+442G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623917 | ||||||
chr11:8623963
|
C | T | 98 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0134others(95): Show | 107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.3019+396G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623963 | ||||||
chr11:8623993
|
C | T | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.3019+366G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623993 | ||||||
chr11:8624057
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3019+302A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8624057 | ||||||
chr11:8624182
|
G | A | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3019+177C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8624182 | ||||||
chr11:8624305
|
G | C | 7 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3019+54C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8624305 | ||||||
chr11:8624690
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(183): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2826+23C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/24 | chr11 | 8624690 | ||||||
chr11:8625249
|
G | C | 1 | a0017c0018t0023g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2311-21C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625249 | ||||||
chr11:8625344
|
TCTGGTAG others(3): Show |
T | 107 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(104): Show | 118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2311-126_2311-117d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625344 | ||||||
chr11:8625453
|
C | T | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2311-225G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625453 | ||||||
chr11:8625463
|
T | TTGTGTG | 10 | a0002c0002t0002g0017a0002c0002t0002g0257a0002c0002t0002g0349others(7): Show | 11 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.2311-241_2311-236d others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(3): Show |
1 | a0002c0002t0002g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2311-245_2311-236d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(5): Show |
5 | a0002c0002t0002g0014a0002c0002t0002g0323a0002c0002t0028g0164others(2): Show | 6 | HG01255.hp1 HG01891.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2311-247_2311-236d others(14): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(7): Show |
8 | a0002c0002t0002g0027a0002c0002t0002g0159a0002c0002t0002g0255others(5): Show | 8 | HG00408.hp2 HG01358.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2311-249_2311-236d others(16): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(9): Show |
40 | a0002c0002t0002g0012a0002c0002t0002g0015a0002c0002t0002g0028others(37): Show | 43 | HG00597.hp2 HG00639.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.2311-251_2311-236d others(18): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(11): Show |
18 | a0002c0002t0002g0003a0002c0002t0002g0124a0002c0002t0002g0162others(15): Show | 20 | HG00280.hp2 HG01106.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2311-253_2311-236d others(20): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(13): Show |
11 | a0002c0002t0002g0010a0002c0002t0002g0013a0002c0002t0002g0125others(8): Show | 13 | HG00408.hp1 HG03491.hp1 HG03491.hp2 others(10): Show |
intron_variant | MODIFIER | c.2311-255_2311-236d others(22): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(15): Show |
1 | a0002c0019t0002g0237 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2311-257_2311-236d others(24): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(17): Show |
1 | a0002c0002t0002g0280 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2311-259_2311-236d others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
T | TTGTGTGT others(19): Show |
2 | a0002c0002t0002g0324a0002c0002t0008g0157 | 2 | NA18964.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2311-261_2311-236d others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
TTG | T | 74 | a0001c0001t0001g0098a0001c0001t0015g0215a0001c0001t0042g0092others(71): Show | 80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2311-237_2311-236d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
TTGTG | T | 94 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(91): Show | 95 | HG00099.hp1 HG00609.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2311-239_2311-236d others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625463
|
TTGTGTG | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(79): Show | 87 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.2311-241_2311-236d others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | ||||||
chr11:8625541
|
TACACACA others(21): Show |
T | 2 | a0003c0003t0005g0009a0003c0003t0005g0152 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2311-341_2311-314d others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625541 | ||||||
chr11:8625543
|
CACACACA others(5): Show |
C | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(81): Show | 89 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.2311-327_2311-316d others(14): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625543 | ||||||
chr11:8625577
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.2311-349G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625577 | ||||||
chr11:8625624
|
C | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(291): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2311-396G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625624 | ||||||
chr11:8625750
|
C | T | 1 | a0002c0002t0002g0259 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2311-522G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625750 | ||||||
chr11:8625841
|
C | T | 2 | a0018c0017t0001g0025a0018c0017t0001g0026 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2311-613G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625841 | ||||||
chr11:8625972
|
C | T | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2311-744G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625972 | ||||||
chr11:8626491
|
G | T | 358 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(355): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.2311-1263C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626491 | ||||||
chr11:8626592
|
C | T | 1 | a0006c0006t0002g0207 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2311-1364G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626592 | ||||||
chr11:8626650
|
T | C | 1 | a0007c0007t0003g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2311-1422A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626650 | ||||||
chr11:8626836
|
T | A | 1 | a0001c0001t0018g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2311-1608A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626836 | ||||||
chr11:8626856
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0080others(22): Show | 26 | HG00280.hp1 HG01070.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.2311-1628C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626856 | ||||||
chr11:8627020
|
G | T | 15 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0087others(12): Show | 15 | HG02040.hp1 HG02132.hp1 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.2311-1792C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627020 | ||||||
chr11:8627143
|
C | T | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2311-1915G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627143 | ||||||
chr11:8627145
|
A | G | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-1917T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627145 | ||||||
chr11:8627168
|
C | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(7): Show | 11 | HG01884.hp1 HG02257.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2311-1940G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627168 | ||||||
chr11:8627249
|
GT | G | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-2022delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627249 | ||||||
chr11:8627295
|
A | C | 4 | a0002c0002t0002g0014a0002c0002t0002g0015a0002c0002t0002g0255others(1): Show | 6 | HG01192.hp1 HG01255.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-2067T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627295 | ||||||
chr11:8627545
|
G | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-2317C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627545 | ||||||
chr11:8627596
|
C | T | 1 | a0017c0018t0024g0030 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2311-2368G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627596 | ||||||
chr11:8627709
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2311-2481A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627709 | ||||||
chr11:8627743
|
T | C | 3 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0078 | 3 | HG00741.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2311-2515A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627743 | ||||||
chr11:8627950
|
G | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(295): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2311-2722C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627950 | ||||||
chr11:8627974
|
G | A | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-2746C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627974 | ||||||
chr11:8628080
|
C | T | 7 | a0001c0001t0001g0295a0001c0001t0001g0297a0001c0001t0001g0298others(4): Show | 7 | NA18939.hp1 NA18946.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-2852G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628080 | ||||||
chr11:8628144
|
C | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(185): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.2311-2916G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628144 | ||||||
chr11:8628150
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2311-2922A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628150 | ||||||
chr11:8628160
|
A | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(180): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2311-2932T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628160 | ||||||
chr11:8628341
|
G | A | 2 | a0001c0001t0018g0034a0001c0001t0018g0035 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2311-3113C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628341 | ||||||
chr11:8628529
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2311-3301G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628529 | ||||||
chr11:8628612
|
C | CA | 83 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(80): Show | 92 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2311-3385dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | ||||||
chr11:8628612
|
C | CAA | 8 | a0002c0002t0002g0163a0002c0002t0002g0268a0002c0002t0002g0288others(5): Show | 8 | HG01891.hp1 HG02738.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.2311-3386_2311-338 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | ||||||
chr11:8628612
|
C | CAAAA | 32 | a0002c0002t0028g0164a0003c0003t0003g0002a0003c0003t0003g0005others(29): Show | 36 | HG00597.hp1 HG00609.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2311-3388_2311-338 others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | ||||||
chr11:8628612
|
C | CAAAAA | 7 | a0003c0003t0003g0055a0003c0003t0003g0146a0003c0003t0003g0153others(4): Show | 7 | HG00735.hp1 HG02071.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-3389_2311-338 others(9): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | ||||||
chr11:8628630
|
A | AAG | 129 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(126): Show | 134 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.2311-3403_2311-340 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628630 | ||||||
chr11:8628630
|
A | AG | 5 | a0001c0001t0001g0019a0001c0001t0001g0143a0001c0001t0001g0221others(2): Show | 5 | HG01070.hp1 HG02922.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-3403_2311-340 others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628630 | ||||||
chr11:8628632
|
A | AGAG | 3 | a0001c0001t0001g0006a0001c0001t0001g0088a0004c0004t0004g0328 | 4 | HG02080.hp1 HG02155.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311-3405_2311-340 others(7): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628632 | ||||||
chr11:8628632
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(131): Show | 139 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.2311-3404T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628632 | ||||||
chr11:8628634
|
A | AGAGAG | 3 | a0013c0013t0019g0120a0013c0013t0019g0121a0013c0013t0047g0054 | 3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2311-3407_2311-340 others(9): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628634 | ||||||
chr11:8628634
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(142): Show | 151 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.2311-3406T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628634 | ||||||
chr11:8628636
|
A | AAAAAAAA others(24): Show |
1 | a0004c0004t0004g0307 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(35): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(23): Show |
1 | a0004c0004t0004g0314 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(21): Show |
1 | a0004c0004t0004g0336 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(19): Show |
1 | a0004c0004t0004g0329 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(18): Show |
2 | a0001c0023t0004g0319a0004c0004t0004g0302 | 2 | HG01192.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(29): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(17): Show |
6 | a0001c0001t0001g0353a0004c0004t0004g0310a0004c0004t0004g0333others(3): Show | 6 | HG00741.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(16): Show |
19 | a0004c0004t0004g0020a0004c0004t0004g0106a0004c0004t0004g0172others(16): Show | 19 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(27): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(15): Show |
4 | a0004c0004t0004g0303a0004c0004t0004g0334a0013c0013t0017g0130others(1): Show | 4 | HG00738.hp1 HG02074.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(17): Show |
4 | a0004c0004t0004g0301a0004c0004t0004g0306a0004c0004t0004g0315others(1): Show | 4 | NA18959.hp1 NA18980.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(14): Show |
1 | a0004c0004t0004g0338 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(25): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(16): Show |
2 | a0004c0004t0004g0356a0004c0004t0016g0322 | 2 | HG01261.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(27): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0168a0004c0021t0039g0318 | 2 | HG00738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(24): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(16): Show |
1 | a0017c0018t0023g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(27): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAAAA others(13): Show |
1 | a0017c0018t0024g0030 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(24): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAAAAGAG others(4): Show |
1 | a0004c0004t0004g0337 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(15): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | AAGAGAG | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-3414_2311-340 others(10): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628636
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(147): Show | 156 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(153): Show |
intron_variant | MODIFIER | c.2311-3408T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | ||||||
chr11:8628713
|
T | G | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-3485A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628713 | ||||||
chr11:8628787
|
T | C | 1 | a0004c0004t0004g0335 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2311-3559A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628787 | ||||||
chr11:8628945
|
A | G | 2 | a0001c0023t0004g0319a0004c0004t0004g0351 | 2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2311-3717T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628945 | ||||||
chr11:8629061
|
A | T | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-3833T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629061 | ||||||
chr11:8629189
|
C | T | 1 | a0003c0003t0006g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2311-3961G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629189 | ||||||
chr11:8629270
|
C | T | 1 | a0006c0006t0002g0249 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2311-4042G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629270 | ||||||
chr11:8629348
|
T | C | 359 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(356): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.2311-4120A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629348 | ||||||
chr11:8629357
|
C | T | 5 | a0004c0004t0004g0304a0015c0014t0004g0305a0015c0014t0004g0308others(2): Show | 5 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.2311-4129G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629357 | ||||||
chr11:8629358
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2311-4130C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629358 | ||||||
chr11:8629584
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0198a0001c0001t0035g0154 | 3 | HG01167.hp2 HG01168.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2311-4356G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629584 | ||||||
chr11:8629623
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0042g0092 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2311-4395C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629623 | ||||||
chr11:8629684
|
T | C | 1 | a0014c0015t0011g0077 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2311-4456A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629684 | ||||||
chr11:8629913
|
C | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0116a0001c0001t0001g0117others(19): Show | 23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2311-4685G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629913 | ||||||
chr11:8629991
|
T | C | 1 | a0019c0020t0003g0194 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2311-4763A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629991 | ||||||
chr11:8630506
|
T | C | 6 | a0001c0001t0001g0066a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-5278A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630506 | ||||||
chr11:8630531
|
G | A | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2311-5303C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630531 | ||||||
chr11:8630697
|
G | A | 1 | a0006c0006t0002g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2311-5469C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630697 | ||||||
chr11:8630711
|
C | T | 1 | a0004c0004t0004g0366 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2311-5483G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630711 | ||||||
chr11:8630763
|
T | C | 1 | a0028c0025t0038g0242 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2311-5535A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630763 | ||||||
chr11:8631045
|
T | C | 97 | a0001c0001t0001g0247a0002c0002t0002g0003a0002c0002t0002g0010others(94): Show | 106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2311-5817A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631045 | ||||||
chr11:8631065
|
T | A | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-5837A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631065 | ||||||
chr11:8631140
|
A | G | 1 | a0003c0003t0003g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2311-5912T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631140 | ||||||
chr11:8631142
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0067others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-5914T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631142 | ||||||
chr11:8631189
|
A | G | 14 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(11): Show | 16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2311-5961T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631189 | ||||||
chr11:8631686
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2311-6458A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631686 | ||||||
chr11:8631768
|
T | C | 1 | a0017c0018t0023g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2311-6540A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631768 | ||||||
chr11:8631812
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(301): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.2311-6584A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631812 | ||||||
chr11:8631951
|
T | C | 1 | a0010c0010t0001g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2310+6703A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631951 | ||||||
chr11:8631960
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0139 | 2 | HG03490.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2310+6694C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631960 | ||||||
chr11:8632079
|
G | A | 2 | a0011c0011t0021g0050a0011c0011t0021g0051 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310+6575C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632079 | ||||||
chr11:8632119
|
C | T | 4 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+6535G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632119 | ||||||
chr11:8632451
|
AT | A | 180 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(177): Show | 189 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(186): Show |
intron_variant | MODIFIER | c.2310+6202delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | ||||||
chr11:8632451
|
ATT | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(154): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.2310+6201_2310+620 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | ||||||
chr11:8632451
|
ATTT | A | 6 | a0008c0008t0007g0361a0013c0013t0019g0120a0013c0013t0019g0121others(3): Show | 6 | HG00323.hp1 HG01099.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2310+6200_2310+620 others(7): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | ||||||
chr11:8632451
|
ATTTT | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+6199_2310+620 others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | ||||||
chr11:8632472
|
T | C | 2 | a0003c0003t0003g0187a0003c0003t0003g0188 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2310+6182A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632472 | ||||||
chr11:8632527
|
C | T | 2 | a0004c0004t0004g0329a0004c0004t0004g0336 | 2 | NA18944.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2310+6127G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632527 | ||||||
chr11:8632640
|
T | G | 3 | a0010c0010t0012g0007a0010c0010t0012g0056a0010c0010t0012g0093 | 4 | HG01884.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2310+6014A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632640 | ||||||
chr11:8632697
|
G | T | 1 | a0001c0001t0040g0022 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2310+5957C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632697 | ||||||
chr11:8632712
|
C | T | 3 | a0011c0011t0021g0050a0011c0011t0021g0051a0011c0011t0027g0218 | 3 | HG02970.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310+5942G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632712 | ||||||
chr11:8632981
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(202): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2310+5673A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632981 | ||||||
chr11:8632991
|
C | A | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+5663G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632991 | ||||||
chr11:8633124
|
C | T | 2 | a0003c0003t0003g0187a0003c0003t0003g0188 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2310+5530G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633124 | ||||||
chr11:8633133
|
T | C | 1 | a0006c0006t0002g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2310+5521A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633133 | ||||||
chr11:8633263
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0087others(2): Show | 5 | NA18960.hp2 NA19006.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+5391C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633263 | ||||||
chr11:8633322
|
C | CA | 64 | a0001c0001t0001g0001a0001c0001t0001g0098a0001c0001t0001g0166others(61): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.2310+5331dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633322 | ||||||
chr11:8633378
|
C | T | 1 | a0026c0036t0017g0367 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2310+5276G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633378 | ||||||
chr11:8633427
|
G | A | 1 | a0012c0012t0009g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2310+5227C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633427 | ||||||
chr11:8633482
|
A | C | 1 | a0007c0007t0003g0175 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2310+5172T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633482 | ||||||
chr11:8633500
|
A | AGT | 22 | a0001c0001t0001g0008a0001c0001t0001g0116a0001c0001t0001g0117others(19): Show | 23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2310+5152_2310+515 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633500 | ||||||
chr11:8633640
|
C | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2310+5014G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633640 | ||||||
chr11:8633712
|
T | C | 1 | a0002c0002t0002g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2310+4942A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633712 | ||||||
chr11:8633805
|
T | C | 14 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(11): Show | 16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2310+4849A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633805 | ||||||
chr11:8633878
|
C | T | 1 | a0020c0038t0001g0068 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2310+4776G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633878 | ||||||
chr11:8633895
|
T | C | 14 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(11): Show | 16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2310+4759A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633895 | ||||||
chr11:8633938
|
C | A | 1 | a0030c0028t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2310+4716G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633938 | ||||||
chr11:8633971
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2310+4683T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633971 | ||||||
chr11:8633990
|
G | C | 3 | a0013c0013t0019g0120a0013c0013t0019g0121a0013c0013t0047g0054 | 3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2310+4664C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633990 | ||||||
chr11:8634212
|
T | C | 1 | a0002c0002t0002g0065 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2310+4442A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634212 | ||||||
chr11:8634319
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2310+4335G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634319 | ||||||
chr11:8634375
|
C | T | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+4279G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634375 | ||||||
chr11:8634453
|
G | C | 1 | a0001c0001t0034g0096 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2310+4201C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634453 | ||||||
chr11:8634488
|
T | C | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+4166A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634488 | ||||||
chr11:8634491
|
T | C | 2 | a0010c0010t0001g0137a0010c0010t0001g0140 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2310+4163A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634491 | ||||||
chr11:8634796
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2310+3858A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634796 | ||||||
chr11:8634895
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0042g0092 | 2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2310+3759T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634895 | ||||||
chr11:8635036
|
A | G | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+3618T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635036 | ||||||
chr11:8635043
|
G | A | 1 | a0003c0003t0003g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2310+3611C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635043 | ||||||
chr11:8635288
|
T | C | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+3366A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635288 | ||||||
chr11:8635322
|
T | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+3332A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635322 | ||||||
chr11:8635455
|
C | A | 7 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(4): Show | 9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.2310+3199G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635455 | ||||||
chr11:8635643
|
T | A | 2 | a0001c0001t0020g0085a0001c0001t0020g0086 | 2 | HG01943.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2310+3011A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635643 | ||||||
chr11:8635739
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2310+2915C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635739 | ||||||
chr11:8635774
|
A | G | 94 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(91): Show | 103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.2310+2880T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635774 | ||||||
chr11:8635969
|
T | C | 2 | a0002c0002t0014g0286a0002c0002t0014g0287 | 2 | NA18954.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2310+2685A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635969 | ||||||
chr11:8636053
|
G | T | 359 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(356): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.2310+2601C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636053 | ||||||
chr11:8636183
|
G | A | 5 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+2471C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636183 | ||||||
chr11:8636376
|
G | A | 7 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(4): Show | 9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.2310+2278C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636376 | ||||||
chr11:8636447
|
A | G | 6 | a0003c0003t0003g0057a0003c0003t0003g0069a0003c0003t0003g0070others(3): Show | 6 | NA18940.hp2 NA18962.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.2310+2207T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636447 | ||||||
chr11:8636486
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2310+2168A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636486 | ||||||
chr11:8636815
|
C | T | 3 | a0011c0011t0021g0050a0011c0011t0021g0051a0011c0011t0027g0218 | 3 | HG02970.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310+1839G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636815 | ||||||
chr11:8636829
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2310+1825G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636829 | ||||||
chr11:8636938
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2310+1716T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636938 | ||||||
chr11:8637321
|
CAT | C | 72 | a0001c0001t0001g0011a0001c0001t0001g0221a0001c0001t0001g0222others(69): Show | 77 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.2310+1331_2310+133 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637321 | ||||||
chr11:8637321
|
CATAT | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2310+1329_2310+133 others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637321 | ||||||
chr11:8637345
|
T | TTA | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+1307_2310+130 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637345 | ||||||
chr11:8637560
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2310+1094G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637560 | ||||||
chr11:8637587
|
G | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(296): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2310+1067C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637587 | ||||||
chr11:8637661
|
C | T | 1 | a0001c0001t0040g0022 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2310+993G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637661 | ||||||
chr11:8637741
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2310+913G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637741 | ||||||
chr11:8637857
|
G | C | 93 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(90): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2310+797C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637857 | ||||||
chr11:8637878
|
G | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+776C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637878 | ||||||
chr11:8637905
|
G | T | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2310+749C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637905 | ||||||
chr11:8637920
|
G | T | 1 | a0004c0021t0039g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2310+734C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637920 | ||||||
chr11:8638361
|
G | A | 4 | a0003c0003t0003g0048a0003c0003t0003g0073a0003c0003t0003g0074others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+293C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638361 | ||||||
chr11:8638410
|
C | G | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2310+244G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638410 | ||||||
chr11:8638414
|
T | C | 1 | a0004c0004t0016g0313 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2310+240A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638414 | ||||||
chr11:8638434
|
A | C | 1 | a0011c0011t0004g0274 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2310+220T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638434 | ||||||
chr11:8638457
|
G | A | 1 | a0004c0004t0004g0363 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2310+197C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638457 | ||||||
chr11:8638514
|
A | C | 1 | a0001c0001t0001g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2310+140T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638514 | ||||||
chr11:8638570
|
C | G | 70 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(67): Show | 79 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.2310+84G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638570 | ||||||
chr11:8638917
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2149-102G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8638917 | ||||||
chr11:8639417
|
G | A | 2 | a0003c0003t0005g0009a0003c0003t0005g0152 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2149-602C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639417 | ||||||
chr11:8639498
|
T | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2149-683A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639498 | ||||||
chr11:8639714
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2148+513G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639714 | ||||||
chr11:8639850
|
C | T | 8 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0193others(5): Show | 11 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2148+377G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639850 | ||||||
chr11:8639942
|
C | T | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+285G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639942 | ||||||
chr11:8639943
|
G | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+284C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639943 | ||||||
chr11:8639998
|
G | A | 8 | a0003c0003t0003g0153a0012c0012t0009g0212a0012c0012t0009g0213others(5): Show | 8 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2148+229C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639998 | ||||||
chr11:8640081
|
T | C | 1 | a0006c0006t0002g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2148+146A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8640081 | ||||||
chr11:8640112
|
C | A | 1 | a0004c0004t0036g0327 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2148+115G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8640112 | ||||||
chr11:8640204
|
C | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0116a0001c0001t0001g0117others(19): Show | 23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2148+23G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8640204 | ||||||
chr11:8641219
|
T | C | 2 | a0004c0004t0004g0330a0004c0004t0004g0331 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1223-67A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641219 | ||||||
chr11:8641488
|
C | G | 62 | a0001c0023t0004g0319a0004c0004t0004g0020a0004c0004t0004g0106others(59): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.1223-336G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641488 | ||||||
chr11:8641551
|
C | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(296): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1223-399G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641551 | ||||||
chr11:8641620
|
G | T | 2 | a0002c0002t0002g0060a0002c0002t0002g0159 | 2 | NA18955.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1223-468C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641620 | ||||||
chr11:8641886
|
C | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1223-734G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641886 | ||||||
chr11:8641887
|
G | A | 1 | a0001c0026t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1223-735C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641887 | ||||||
chr11:8642083
|
G | A | 18 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0091others(15): Show | 19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1222+926C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642083 | ||||||
chr11:8642087
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+922G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642087 | ||||||
chr11:8642106
|
G | A | 1 | a0003c0003t0003g0357 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1222+903C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642106 | ||||||
chr11:8642222
|
T | A | 1 | a0007c0007t0003g0175 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1222+787A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642222 | ||||||
chr11:8642423
|
C | T | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+586G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642423 | ||||||
chr11:8642472
|
A | G | 9 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0193others(6): Show | 12 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+537T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642472 | ||||||
chr11:8642570
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0199 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1222+439C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642570 | ||||||
chr11:8642610
|
C | A | 3 | a0011c0011t0021g0050a0011c0011t0021g0051a0011c0011t0027g0218 | 3 | HG02970.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+399G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642610 | ||||||
chr11:8642832
|
C | G | 2 | a0003c0003t0003g0112a0003c0003t0003g0113 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1222+177G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642832 | ||||||
chr11:8642843
|
C | CA | 6 | a0003c0003t0003g0071a0003c0003t0003g0153a0003c0003t0003g0182others(3): Show | 6 | HG00735.hp1 NA18953.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+165dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | ||||||
chr11:8642843
|
C | CAA | 7 | a0002c0002t0002g0029a0002c0002t0002g0049a0002c0002t0002g0065others(4): Show | 7 | HG01516.hp1 HG02451.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+164_1222+165d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | ||||||
chr11:8642843
|
C | CAAA | 77 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(74): Show | 84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1222+163_1222+165d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | ||||||
chr11:8642843
|
C | CAAAA | 13 | a0002c0002t0002g0014a0002c0002t0002g0015a0002c0002t0002g0162others(10): Show | 15 | HG01167.hp1 HG01169.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1222+162_1222+165d others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | ||||||
chr11:8642843
|
CA | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(168): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1222+165delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | ||||||
chr11:8642843
|
CAA | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0198a0001c0001t0001g0341others(7): Show | 12 | HG00099.hp2 HG00323.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+164_1222+165d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | ||||||
chr11:8642843
|
CAAA | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+163_1222+165d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | ||||||
chr11:8642907
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(199): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1222+102T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642907 | ||||||
chr11:8643287
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1105-161A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643287 | ||||||
chr11:8643322
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(297): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1105-196G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643322 | ||||||
chr11:8643337
|
C | CTTT | 6 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(3): Show | 8 | HG00099.hp2 HG01952.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1105-214_1105-212d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643337 | ||||||
chr11:8643337
|
CT | C | 55 | a0001c0001t0020g0086a0002c0002t0002g0163a0003c0003t0003g0002others(52): Show | 59 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1105-212delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643337 | ||||||
chr11:8643363
|
G | A | 37 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(34): Show | 44 | HG00280.hp2 HG00597.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105-237C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643363 | ||||||
chr11:8643496
|
C | G | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105-370G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643496 | ||||||
chr11:8643603
|
A | C | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1105-477T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643603 | ||||||
chr11:8643732
|
C | T | 3 | a0004c0004t0004g0309a0004c0004t0004g0310a0004c0004t0004g0335 | 3 | HG02083.hp1 NA19011.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1105-606G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643732 | ||||||
chr11:8643848
|
C | T | 1 | a0013c0013t0017g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1105-722G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643848 | ||||||
chr11:8643949
|
C | T | 7 | a0002c0002t0002g0065a0002c0002t0002g0259a0002c0002t0002g0260others(4): Show | 7 | NA18950.hp2 NA18969.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-823G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643949 | ||||||
chr11:8644162
|
T | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0088a0001c0001t0001g0099others(3): Show | 7 | HG01175.hp1 HG02080.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1036A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644162 | ||||||
chr11:8644219
|
A | C | 2 | a0013c0013t0017g0130a0013c0013t0046g0052 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1105-1093T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644219 | ||||||
chr11:8644221
|
C | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1095G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644221 | ||||||
chr11:8644442
|
G | GA | 5 | a0001c0001t0001g0089a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104+1298dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644442 | ||||||
chr11:8644494
|
C | A | 1 | a0001c0001t0037g0352 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1104+1247G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644494 | ||||||
chr11:8644769
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1104+972G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644769 | ||||||
chr11:8644843
|
A | G | 3 | a0006c0006t0002g0240a0006c0006t0002g0249a0006c0006t0002g0250 | 3 | HG02145.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1104+898T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644843 | ||||||
chr11:8644864
|
G | A | 1 | a0004c0004t0004g0334 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1104+877C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644864 | ||||||
chr11:8645230
|
T | G | 1 | a0001c0001t0043g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1104+511A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645230 | ||||||
chr11:8645429
|
C | G | 45 | a0001c0023t0004g0319a0004c0004t0004g0020a0004c0004t0004g0106others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1104+312G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645429 | ||||||
chr11:8645432
|
G | C | 2 | a0001c0001t0020g0085a0001c0001t0020g0086 | 2 | HG01943.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1104+309C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645432 | ||||||
chr11:8645477
|
TC | T | 10 | a0002c0002t0002g0060a0002c0002t0002g0156a0002c0002t0002g0158others(7): Show | 10 | HG00408.hp2 HG02083.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1104+263delG | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645477 | ||||||
chr11:8645968
|
T | C | 4 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-81A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/24 | chr11 | 8645968 | ||||||
chr11:8646133
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.958-246A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/24 | chr11 | 8646133 | ||||||
chr11:8646633
|
A | G | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.843-72T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646633 | ||||||
chr11:8646803
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.843-242C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646803 | ||||||
chr11:8646855
|
G | A | 1 | a0006c0006t0002g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843-294C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646855 | ||||||
chr11:8646941
|
TGCCTC | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(295): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.843-385_843-381del others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646941 | ||||||
chr11:8647022
|
A | G | 93 | a0001c0001t0001g0247a0002c0002t0002g0003a0002c0002t0002g0010others(90): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.843-461T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647022 | ||||||
chr11:8647089
|
CAT | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.843-530_843-529del others(2): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647089 | ||||||
chr11:8647173
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.843-612C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647173 | ||||||
chr11:8647445
|
GAA | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(288): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.842+523_842+524del others(2): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647445 | ||||||
chr11:8647460
|
A | T | 1 | a0002c0002t0002g0012 | 2 | NA19009.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.842+510T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647460 | ||||||
chr11:8647537
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.842+433G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647537 | ||||||
chr11:8647585
|
C | A | 1 | a0001c0001t0001g0297 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.842+385G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647585 | ||||||
chr11:8647612
|
A | G | 3 | a0013c0013t0019g0120a0013c0013t0019g0121a0013c0013t0047g0054 | 3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.842+358T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647612 | ||||||
chr11:8647695
|
C | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+275G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647695 | ||||||
chr11:8647870
|
T | C | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.842+100A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647870 | ||||||
chr11:8647890
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(185): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.842+80T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647890 | ||||||
chr11:8647897
|
G | A | 1 | a0002c0002t0002g0290 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.842+73C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647897 | ||||||
chr11:8647963
|
G | A | 2 | a0011c0011t0021g0050a0011c0011t0021g0051 | 2 | HG02970.hp1 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.842+7C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647963 | ||||||
chr11:8648147
|
C | T | 143 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(140): Show | 156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.726-61G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648147 | ||||||
chr11:8648301
|
C | T | 1 | a0029c0027t0001g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.725+115G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648301 | ||||||
chr11:8648327
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0097 | 2 | HG06807.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.725+89C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648327 | ||||||
chr11:8648360
|
C | G | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.725+56G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648360 | ||||||
chr11:8648376
|
A | G | 1 | a0006c0006t0002g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.725+40T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648376 | ||||||
chr11:8648625
|
T | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(342): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.593-77A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648625 | ||||||
chr11:8648720
|
T | G | 2 | a0002c0002t0002g0028a0002c0002t0002g0029 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.593-172A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648720 | ||||||
chr11:8648784
|
A | G | 4 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-236T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648784 | ||||||
chr11:8648796
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0243 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.593-248G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648796 | ||||||
chr11:8648970
|
G | A | 6 | a0003c0003t0003g0048a0003c0003t0003g0073a0003c0003t0003g0074others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-422C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648970 | ||||||
chr11:8649184
|
C | T | 1 | a0001c0001t0043g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.592+556G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649184 | ||||||
chr11:8649200
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(192): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.592+540C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649200 | ||||||
chr11:8649229
|
C | T | 1 | a0004c0004t0004g0302 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.592+511G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649229 | ||||||
chr11:8649265
|
G | A | 3 | a0013c0013t0019g0120a0013c0013t0019g0121a0013c0013t0047g0054 | 3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.592+475C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649265 | ||||||
chr11:8649442
|
G | T | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.592+298C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649442 | ||||||
chr11:8649507
|
T | C | 1 | a0002c0002t0002g0324 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.592+233A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649507 | ||||||
chr11:8649563
|
G | A | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.592+177C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649563 | ||||||
chr11:8649659
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02922.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+81G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649659 | ||||||
chr11:8649716
|
G | GGCAGGGA others(14): Show |
7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+3_592+23dupACC others(18): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649716 | ||||||
chr11:8649897
|
G | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | NA19000.hp1 NA19063.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.445-10C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8649897 | ||||||
chr11:8649944
|
C | G | 1 | a0017c0018t0023g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.445-57G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8649944 | ||||||
chr11:8649957
|
C | T | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.445-70G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8649957 | ||||||
chr11:8650000
|
G | A | 150 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(147): Show | 163 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.445-113C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650000 | ||||||
chr11:8650041
|
C | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-154G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650041 | ||||||
chr11:8650115
|
G | A | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.445-228C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650115 | ||||||
chr11:8650229
|
C | T | 6 | a0003c0003t0003g0048a0003c0003t0003g0073a0003c0003t0003g0074others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-342G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650229 | ||||||
chr11:8650450
|
G | A | 3 | a0013c0013t0019g0120a0013c0013t0019g0121a0013c0013t0047g0054 | 3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.445-563C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650450 | ||||||
chr11:8650517
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.445-630C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650517 | ||||||
chr11:8650564
|
C | T | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-677G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650564 | ||||||
chr11:8650713
|
G | A | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-826C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650713 | ||||||
chr11:8650793
|
G | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-906C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650793 | ||||||
chr11:8651253
|
A | G | 2 | a0013c0013t0017g0130a0013c0013t0046g0052 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.444+547T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8651253 | ||||||
chr11:8651443
|
T | C | 2 | a0002c0002t0002g0258a0002c0002t0002g0290 | 2 | HG02071.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.444+357A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8651443 | ||||||
chr11:8651933
|
G | A | 1 | a0011c0011t0021g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.341-30C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8651933 | ||||||
chr11:8652041
|
C | T | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.341-138G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652041 | ||||||
chr11:8652169
|
A | G | 33 | a0002c0002t0002g0014a0002c0002t0002g0015a0002c0002t0002g0060others(30): Show | 35 | HG00408.hp2 HG00621.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.341-266T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652169 | ||||||
chr11:8652179
|
A | G | 1 | a0007c0007t0026g0169 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.341-276T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652179 | ||||||
chr11:8652186
|
A | C | 1 | a0004c0004t0036g0327 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.341-283T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652186 | ||||||
chr11:8652392
|
C | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.341-489G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652392 | ||||||
chr11:8652502
|
A | T | 349 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(346): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.341-599T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652502 | ||||||
chr11:8652541
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.341-638A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652541 | ||||||
chr11:8652653
|
A | T | 9 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(6): Show | 9 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-750T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652653 | ||||||
chr11:8652834
|
C | T | 1 | a0006c0006t0002g0047 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.341-931G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652834 | ||||||
chr11:8652835
|
G | A | 1 | a0003c0003t0003g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.341-932C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652835 | ||||||
chr11:8652903
|
C | T | 359 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(356): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.341-1000G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652903 | ||||||
chr11:8653058
|
T | C | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.341-1155A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653058 | ||||||
chr11:8653107
|
C | T | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1204G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653107 | ||||||
chr11:8653464
|
T | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1561A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653464 | ||||||
chr11:8653519
|
G | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1616C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653519 | ||||||
chr11:8653539
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(179): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.341-1636A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653539 | ||||||
chr11:8653735
|
T | C | 1 | a0002c0002t0002g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-1832A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653735 | ||||||
chr11:8653781
|
C | T | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1878G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653781 | ||||||
chr11:8653787
|
C | CAA | 9 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(6): Show | 9 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-1886_341-1885d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653787 | ||||||
chr11:8653897
|
C | CAAGAACA others(2307): Show |
1 | a0012c0012t0009g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2316): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2306): Show |
1 | a0012c0012t0009g0228 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2315): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2307): Show |
1 | a0012c0012t0009g0227 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2316): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2309): Show |
1 | a0023c0033t0032g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2318): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2306): Show |
1 | a0012c0012t0009g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2315): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2305): Show |
1 | a0012c0012t0009g0214 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2314): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2307): Show |
1 | a0022c0029t0009g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2316): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2254): Show |
1 | a0017c0018t0024g0030 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2263): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653897
|
C | CAAGAACA others(2008): Show |
1 | a0017c0018t0023g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2017): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | ||||||
chr11:8653928
|
C | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(198): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.341-2025G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653928 | ||||||
chr11:8654282
|
G | A | 6 | a0009c0009t0001g0021a0009c0009t0001g0037a0009c0009t0001g0038others(3): Show | 6 | HG00621.hp2 HG02015.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-2379C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654282 | ||||||
chr11:8654637
|
T | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG00140.hp1 HG01243.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-2734A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654637 | ||||||
chr11:8654691
|
C | T | 143 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(140): Show | 156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.341-2788G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654691 | ||||||
chr11:8654741
|
T | C | 6 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0200others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-2838A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654741 | ||||||
chr11:8654918
|
C | T | 5 | a0002c0002t0002g0013a0002c0002t0002g0217a0002c0002t0002g0280others(2): Show | 6 | HG03209.hp1 NA18946.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-3015G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654918 | ||||||
chr11:8655035
|
T | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-3132A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655035 | ||||||
chr11:8655092
|
T | C | 1 | a0002c0002t0002g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-3189A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655092 | ||||||
chr11:8655178
|
G | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(9): Show | 13 | HG01884.hp1 HG01943.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-3275C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655178 | ||||||
chr11:8655361
|
T | C | 1 | a0005c0005t0002g0263 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.341-3458A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655361 | ||||||
chr11:8655484
|
C | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0199 | 3 | HG01099.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.341-3581G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655484 | ||||||
chr11:8655485
|
G | GT | 11 | a0001c0001t0001g0101a0001c0001t0001g0234a0001c0001t0001g0341others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-3583dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655485 | ||||||
chr11:8655516
|
C | A | 142 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(139): Show | 155 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.341-3613G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655516 | ||||||
chr11:8655638
|
T | C | 157 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(154): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.341-3735A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655638 | ||||||
chr11:8655654
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(179): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.341-3751C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655654 | ||||||
chr11:8655674
|
C | T | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.341-3771G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655674 | ||||||
chr11:8655724
|
G | A | 4 | a0009c0009t0001g0037a0009c0009t0001g0038a0009c0009t0001g0043others(1): Show | 4 | HG02015.hp2 NA18951.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-3821C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655724 | ||||||
chr11:8655966
|
AGAGCAGA others(4): Show |
A | 1 | a0007c0007t0003g0176 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.341-4074_341-4064d others(13): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655966 | ||||||
chr11:8656314
|
T | A | 1 | a0004c0004t0004g0337 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.341-4411A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656314 | ||||||
chr11:8656345
|
T | C | 2 | a0003c0003t0003g0187a0003c0003t0003g0188 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.341-4442A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656345 | ||||||
chr11:8656729
|
C | G | 1 | a0001c0001t0022g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.341-4826G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656729 | ||||||
chr11:8656973
|
T | C | 5 | a0002c0002t0002g0273a0002c0002t0002g0324a0002c0002t0014g0286others(2): Show | 5 | NA18954.hp1 NA18964.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-5070A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656973 | ||||||
chr11:8657085
|
C | A | 2 | a0001c0001t0018g0034a0001c0001t0018g0035 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.341-5182G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657085 | ||||||
chr11:8657209
|
G | A | 166 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(163): Show | 180 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.341-5306C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657209 | ||||||
chr11:8657321
|
C | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-5418G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657321 | ||||||
chr11:8657444
|
C | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-5541G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657444 | ||||||
chr11:8657469
|
G | A | 180 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(177): Show | 196 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.341-5566C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657469 | ||||||
chr11:8657559
|
G | A | 1 | a0004c0004t0004g0334 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.341-5656C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657559 | ||||||
chr11:8657781
|
C | T | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | NA18939.hp1 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.341-5878G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657781 | ||||||
chr11:8657999
|
C | T | 9 | a0006c0006t0002g0036a0006c0006t0002g0047a0006c0006t0002g0207others(6): Show | 9 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-6096G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657999 | ||||||
chr11:8658077
|
G | A | 1 | a0006c0006t0002g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.341-6174C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658077 | ||||||
chr11:8658229
|
C | T | 1 | a0001c0001t0018g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.341-6326G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658229 | ||||||
chr11:8658480
|
C | G | 1 | a0013c0013t0046g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.341-6577G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658480 | ||||||
chr11:8658537
|
G | A | 2 | a0001c0001t0015g0229a0001c0001t0015g0354 | 2 | HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.341-6634C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658537 | ||||||
chr11:8658834
|
G | A | 5 | a0010c0010t0001g0137a0010c0010t0001g0140a0010c0010t0012g0007others(2): Show | 6 | HG01884.hp2 HG02055.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-6931C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658834 | ||||||
chr11:8658917
|
T | C | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.341-7014A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658917 | ||||||
chr11:8659269
|
T | G | 8 | a0003c0003t0005g0009a0003c0003t0005g0151a0003c0003t0005g0152others(5): Show | 9 | HG01109.hp2 HG01346.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-7366A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659269 | ||||||
chr11:8659338
|
T | G | 62 | a0002c0002t0002g0360a0002c0002t0028g0164a0003c0003t0003g0002others(59): Show | 66 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.341-7435A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659338 | ||||||
chr11:8659344
|
T | C | 166 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(163): Show | 180 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.341-7441A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659344 | ||||||
chr11:8659466
|
G | C | 1 | a0013c0013t0046g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.341-7563C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659466 | ||||||
chr11:8659891
|
G | C | 31 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0079others(28): Show | 34 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.341-7988C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659891 | ||||||
chr11:8659894
|
T | C | 2 | a0018c0017t0001g0025a0018c0017t0001g0026 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.341-7991A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659894 | ||||||
chr11:8660014
|
A | T | 1 | a0030c0028t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.341-8111T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660014 | ||||||
chr11:8660312
|
G | A | 1 | a0013c0013t0017g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.341-8409C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660312 | ||||||
chr11:8660471
|
C | T | 171 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(168): Show | 184 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.341-8568G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660471 | ||||||
chr11:8660731
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.341-8828G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660731 | ||||||
chr11:8660822
|
G | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(9): Show | 13 | HG01884.hp1 HG01943.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-8919C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660822 | ||||||
chr11:8660918
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(64): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.341-9015A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660918 | ||||||
chr11:8661092
|
G | A | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-9189C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661092 | ||||||
chr11:8661253
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.341-9350C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661253 | ||||||
chr11:8661272
|
G | A | 1 | a0003c0003t0003g0216 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.341-9369C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661272 | ||||||
chr11:8661406
|
C | A | 1 | a0014c0015t0011g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.341-9503G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661406 | ||||||
chr11:8661428
|
C | T | 1 | a0002c0002t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.341-9525G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661428 | ||||||
chr11:8661672
|
C | T | 1 | a0001c0001t0015g0215 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.341-9769G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661672 | ||||||
chr11:8661807
|
A | T | 17 | a0001c0001t0001g0044a0001c0001t0001g0289a0001c0001t0001g0325others(14): Show | 17 | HG00609.hp2 HG00621.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.341-9904T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661807 | ||||||
chr11:8662000
|
T | C | 1 | a0011c0011t0021g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.340+9786A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662000 | ||||||
chr11:8662092
|
C | T | 171 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(168): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.340+9694G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662092 | ||||||
chr11:8662212
|
C | T | 8 | a0003c0003t0005g0009a0003c0003t0005g0151a0003c0003t0005g0152others(5): Show | 9 | HG01109.hp2 HG01346.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+9574G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662212 | ||||||
chr11:8662490
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.340+9296C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662490 | ||||||
chr11:8662504
|
C | T | 6 | a0003c0003t0003g0048a0003c0003t0003g0073a0003c0003t0003g0074others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+9282G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662504 | ||||||
chr11:8662903
|
G | T | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.340+8883C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662903 | ||||||
chr11:8662991
|
T | G | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+8795A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662991 | ||||||
chr11:8663205
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.340+8581T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663205 | ||||||
chr11:8663374
|
T | C | 2 | a0001c0001t0020g0085a0001c0001t0020g0086 | 2 | HG01943.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.340+8412A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663374 | ||||||
chr11:8663434
|
C | T | 1 | a0003c0003t0003g0232 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.340+8352G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663434 | ||||||
chr11:8663477
|
T | TAAGAATA others(342): Show |
1 | a0001c0001t0001g0099 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.340+8308_340+8309i others(351): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663477 | ||||||
chr11:8663564
|
T | A | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+8222A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663564 | ||||||
chr11:8663783
|
T | C | 1 | a0002c0002t0002g0288 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.340+8003A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663783 | ||||||
chr11:8663805
|
A | G | 9 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(6): Show | 9 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+7981T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663805 | ||||||
chr11:8663846
|
C | T | 161 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(158): Show | 175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.340+7940G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663846 | ||||||
chr11:8663904
|
C | A | 13 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+7882G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663904 | ||||||
chr11:8664101
|
T | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+7685A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664101 | ||||||
chr11:8664138
|
A | C | 144 | a0001c0001t0001g0122a0002c0002t0002g0003a0002c0002t0002g0010others(141): Show | 157 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.340+7648T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664138 | ||||||
chr11:8664154
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.340+7632G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664154 | ||||||
chr11:8664204
|
C | T | 1 | a0004c0021t0039g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.340+7582G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664204 | ||||||
chr11:8664206
|
T | C | 1 | a0003c0003t0003g0183 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.340+7580A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664206 | ||||||
chr11:8664271
|
A | T | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+7515T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664271 | ||||||
chr11:8664471
|
G | A | 3 | a0004c0004t0004g0309a0004c0004t0004g0310a0004c0004t0004g0335 | 3 | HG02083.hp1 NA19011.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.340+7315C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664471 | ||||||
chr11:8664486
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.340+7300A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664486 | ||||||
chr11:8664521
|
A | G | 60 | a0002c0002t0002g0360a0002c0002t0028g0164a0003c0003t0003g0002others(57): Show | 64 | HG00323.hp2 HG00609.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.340+7265T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664521 | ||||||
chr11:8664787
|
G | A | 1 | a0002c0002t0044g0292 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.340+6999C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664787 | ||||||
chr11:8665116
|
T | TA | 10 | a0002c0002t0002g0162a0003c0003t0003g0048a0003c0003t0003g0073others(7): Show | 10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+6669dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665116 | ||||||
chr11:8665300
|
C | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+6486G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665300 | ||||||
chr11:8665637
|
A | G | 1 | a0022c0029t0009g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.340+6149T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665637 | ||||||
chr11:8665691
|
C | T | 1 | a0007c0007t0003g0063 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.340+6095G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665691 | ||||||
chr11:8665744
|
T | G | 1 | a0001c0001t0022g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340+6042A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665744 | ||||||
chr11:8665805
|
C | T | 1 | a0001c0001t0022g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340+5981G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665805 | ||||||
chr11:8665806
|
G | A | 5 | a0002c0002t0002g0017a0002c0002t0002g0248a0002c0002t0002g0268others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+5980C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665806 | ||||||
chr11:8665886
|
T | C | 1 | a0003c0003t0003g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+5900A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665886 | ||||||
chr11:8666095
|
G | A | 3 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029 | 3 | HG01516.hp1 HG01517.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.340+5691C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666095 | ||||||
chr11:8666158
|
G | A | 161 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(158): Show | 175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.340+5628C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666158 | ||||||
chr11:8666163
|
C | G | 143 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(140): Show | 156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.340+5623G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666163 | ||||||
chr11:8666251
|
A | C | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+5535T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666251 | ||||||
chr11:8666272
|
G | A | 5 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+5514C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666272 | ||||||
chr11:8666294
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0325a0001c0001t0001g0326 | 3 | NA18962.hp1 NA18990.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.340+5492C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666294 | ||||||
chr11:8666341
|
G | GA | 44 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0104others(41): Show | 44 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.340+5444dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | ||||||
chr11:8666341
|
GA | G | 33 | a0001c0001t0001g0058a0001c0001t0001g0081a0001c0001t0001g0090others(30): Show | 34 | HG01168.hp1 HG01496.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.340+5444delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | ||||||
chr11:8666341
|
GAA | G | 19 | a0001c0001t0001g0148a0003c0003t0003g0048a0003c0003t0003g0073others(16): Show | 20 | HG01109.hp2 HG01346.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.340+5443_340+5444d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | ||||||
chr11:8666341
|
GAAAAAAA others(3): Show |
G | 2 | a0017c0018t0023g0119a0017c0018t0024g0030 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.340+5435_340+5444d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | ||||||
chr11:8666341
|
GAAAAAAA others(6): Show |
G | 4 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(1): Show | 4 | HG00741.hp1 HG02145.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+5432_340+5444d others(15): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | ||||||
chr11:8666341
|
GAAAAAAA others(7): Show |
G | 1 | a0014c0015t0011g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.340+5431_340+5444d others(16): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | ||||||
chr11:8666355
|
A | AG | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+5430_340+5431i others(3): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666355 | ||||||
chr11:8666370
|
G | C | 1 | a0001c0001t0022g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340+5416C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666370 | ||||||
chr11:8666469
|
C | T | 185 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(182): Show | 201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+5317G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666469 | ||||||
chr11:8666538
|
G | A | 1 | a0003c0003t0003g0184 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.340+5248C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666538 | ||||||
chr11:8666578
|
C | A | 180 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(177): Show | 194 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.340+5208G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666578 | ||||||
chr11:8666744
|
A | T | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+5042T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666744 | ||||||
chr11:8666772
|
T | C | 10 | a0003c0003t0003g0048a0003c0003t0003g0073a0003c0003t0003g0074others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+5014A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666772 | ||||||
chr11:8667190
|
AT | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0198a0001c0001t0035g0154 | 3 | HG01167.hp2 HG01168.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.340+4595delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667190 | ||||||
chr11:8667375
|
A | C | 13 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029others(10): Show | 13 | HG00408.hp1 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+4411T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667375 | ||||||
chr11:8667465
|
A | G | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+4321T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667465 | ||||||
chr11:8667620
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.340+4166T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667620 | ||||||
chr11:8667653
|
A | C | 5 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+4133T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667653 | ||||||
chr11:8667700
|
T | C | 1 | a0002c0002t0002g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340+4086A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667700 | ||||||
chr11:8667789
|
C | T | 185 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(182): Show | 201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+3997G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667789 | ||||||
chr11:8667882
|
C | A | 3 | a0003c0003t0003g0073a0003c0003t0003g0074a0003c0003t0003g0129 | 3 | HG02615.hp2 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.340+3904G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667882 | ||||||
chr11:8667967
|
C | T | 19 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(16): Show | 21 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.340+3819G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667967 | ||||||
chr11:8668158
|
C | G | 1 | a0012c0012t0009g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340+3628G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668158 | ||||||
chr11:8668199
|
T | C | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+3587A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668199 | ||||||
chr11:8668264
|
GT | G | 8 | a0001c0001t0001g0033a0012c0012t0009g0212a0012c0012t0009g0213others(5): Show | 8 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+3521delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668264 | ||||||
chr11:8668364
|
G | A | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+3422C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668364 | ||||||
chr11:8668541
|
T | C | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.340+3245A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668541 | ||||||
chr11:8668565
|
T | A | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+3221A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668565 | ||||||
chr11:8668590
|
A | T | 1 | a0014c0015t0011g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.340+3196T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668590 | ||||||
chr11:8668590
|
AT | A | 15 | a0003c0003t0003g0147a0008c0008t0007g0004a0008c0008t0007g0197others(12): Show | 17 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.340+3195delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668590 | ||||||
chr11:8668594
|
T | A | 11 | a0001c0001t0001g0033a0003c0003t0003g0048a0003c0003t0003g0073others(8): Show | 11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+3192A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668594 | ||||||
chr11:8668595
|
T | A | 7 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(4): Show | 9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+3191A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668595 | ||||||
chr11:8668671
|
C | T | 36 | a0003c0003t0003g0002a0003c0003t0003g0005a0003c0003t0003g0055others(33): Show | 40 | HG00609.hp1 HG00735.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.340+3115G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668671 | ||||||
chr11:8668710
|
C | G | 143 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(140): Show | 156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.340+3076G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668710 | ||||||
chr11:8668743
|
G | A | 1 | a0014c0015t0011g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.340+3043C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668743 | ||||||
chr11:8669027
|
T | C | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+2759A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669027 | ||||||
chr11:8669159
|
T | C | 1 | a0001c0001t0010g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.340+2627A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669159 | ||||||
chr11:8669171
|
T | C | 143 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(140): Show | 156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.340+2615A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669171 | ||||||
chr11:8669225
|
C | T | 5 | a0006c0006t0002g0240a0006c0006t0002g0249a0006c0006t0002g0250others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+2561G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669225 | ||||||
chr11:8669311
|
T | C | 1 | a0013c0013t0046g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.340+2475A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669311 | ||||||
chr11:8669317
|
C | T | 1 | a0004c0004t0004g0366 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.340+2469G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669317 | ||||||
chr11:8669367
|
G | A | 3 | a0002c0002t0014g0286a0002c0002t0014g0287a0002c0002t0014g0293 | 3 | NA18954.hp1 NA18975.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.340+2419C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669367 | ||||||
chr11:8669465
|
G | A | 171 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(168): Show | 185 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.340+2321C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669465 | ||||||
chr11:8669530
|
G | A | 1 | a0003c0003t0003g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+2256C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669530 | ||||||
chr11:8669547
|
G | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+2239C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669547 | ||||||
chr11:8669597
|
C | A | 10 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(7): Show | 10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+2189G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669597 | ||||||
chr11:8669611
|
C | A | 1 | a0013c0013t0047g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340+2175G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669611 | ||||||
chr11:8669642
|
C | CA | 17 | a0001c0001t0001g0024a0001c0001t0001g0101a0001c0001t0001g0102others(14): Show | 17 | HG00140.hp2 HG01175.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.340+2143dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669642 | ||||||
chr11:8669642
|
CA | C | 173 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(170): Show | 189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.340+2143delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669642 | ||||||
chr11:8669657
|
A | C | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+2129T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669657 | ||||||
chr11:8669801
|
C | T | 1 | a0007c0007t0026g0169 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.340+1985G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669801 | ||||||
chr11:8669805
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.340+1981G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669805 | ||||||
chr11:8669855
|
T | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0289a0001c0001t0001g0325others(6): Show | 9 | NA18962.hp1 NA18981.hp1 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+1931A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669855 | ||||||
chr11:8669984
|
A | G | 1 | a0001c0001t0001g0006 | 2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.340+1802T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669984 | ||||||
chr11:8670007
|
G | GT | 3 | a0002c0002t0008g0126a0002c0002t0008g0155a0002c0002t0008g0157 | 3 | NA18956.hp1 NA18964.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.340+1778dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670007 | ||||||
chr11:8670012
|
TA | T | 70 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(67): Show | 78 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.340+1773delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670012 | ||||||
chr11:8670013
|
A | AT | 9 | a0003c0003t0005g0009a0003c0003t0005g0151a0003c0003t0005g0152others(6): Show | 10 | HG01109.hp2 HG01346.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.340+1772dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670013 | ||||||
chr11:8670013
|
A | T | 19 | a0002c0002t0002g0013a0002c0002t0002g0027a0002c0002t0002g0028others(16): Show | 20 | HG00408.hp1 HG01515.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.340+1773T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670013 | ||||||
chr11:8670017
|
A | AT | 62 | a0001c0001t0001g0219a0001c0001t0001g0220a0002c0002t0002g0193others(59): Show | 66 | HG00323.hp2 HG00609.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.340+1768dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670017 | ||||||
chr11:8670017
|
A | T | 123 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(120): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.340+1769T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670017 | ||||||
chr11:8670019
|
T | A | 17 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(14): Show | 19 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.340+1767A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670019 | ||||||
chr11:8670166
|
C | A | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1620G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670166 | ||||||
chr11:8670172
|
C | T | 10 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(7): Show | 10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+1614G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670172 | ||||||
chr11:8670173
|
C | T | 12 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0002g0029others(9): Show | 12 | HG00408.hp1 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.340+1613G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670173 | ||||||
chr11:8670233
|
G | A | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1553C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670233 | ||||||
chr11:8670264
|
G | T | 5 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(2): Show | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+1522C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670264 | ||||||
chr11:8670301
|
T | C | 10 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(7): Show | 10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+1485A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670301 | ||||||
chr11:8670414
|
T | C | 1 | a0006c0006t0002g0275 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340+1372A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670414 | ||||||
chr11:8670792
|
G | A | 185 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(182): Show | 201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+994C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670792 | ||||||
chr11:8671019
|
C | T | 14 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(11): Show | 16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.340+767G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671019 | ||||||
chr11:8671067
|
G | A | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.340+719C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671067 | ||||||
chr11:8671217
|
GATATTCA others(4): Show |
G | 1 | a0001c0001t0001g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.340+558_340+568del others(11): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671217 | ||||||
chr11:8671369
|
CA | C | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+416delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671369 | ||||||
chr11:8671408
|
T | C | 10 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(7): Show | 10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+378A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671408 | ||||||
chr11:8671627
|
C | T | 1 | a0002c0019t0030g0368 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.340+159G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671627 | ||||||
chr11:8671722
|
C | T | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+64G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671722 | ||||||
chr11:8671785
|
C | G | 2 | a0016c0016t0002g0346a0016c0016t0002g0347 | 2 | HG03669.hp2 HG03710.hp1 |
splice_donor_variant&intron_variant | HIGH | c.340+1G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671785 | ||||||
chr11:8672526
|
G | C | 186 | a0001c0001t0001g0066a0002c0002t0002g0003a0002c0002t0002g0010others(183): Show | 202 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-111-141C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672526 | ||||||
chr11:8672619
|
C | CT | 4 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(1): Show | 6 | HG00099.hp2 HG01952.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-235dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672619 | ||||||
chr11:8672619
|
CT | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(278): Show | 297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.-111-235delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672619 | ||||||
chr11:8672619
|
CTT | C | 8 | a0001c0001t0001g0080a0001c0001t0001g0343a0004c0004t0004g0345others(5): Show | 8 | HG01099.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-236_-111-235d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672619 | ||||||
chr11:8672637
|
T | C | 6 | a0003c0003t0006g0170a0003c0003t0006g0185a0003c0003t0006g0186others(3): Show | 6 | HG00642.hp2 HG01123.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111-252A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672637 | ||||||
chr11:8672701
|
G | A | 6 | a0012c0012t0009g0213a0012c0012t0009g0214a0012c0012t0009g0227others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-316C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672701 | ||||||
chr11:8672935
|
C | CTA | 4 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(1): Show | 6 | HG00099.hp2 HG01952.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-551_-111-550i others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672935 | ||||||
chr11:8672936
|
T | TA | 3 | a0008c0008t0007g0361a0017c0018t0023g0119a0017c0018t0024g0030 | 3 | HG00323.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-111-552_-111-551i others(3): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672936 | ||||||
chr11:8672937
|
C | T | 7 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(4): Show | 9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-552G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672937 | ||||||
chr11:8672937
|
CT | C | 157 | a0001c0001t0001g0044a0001c0001t0001g0105a0001c0001t0001g0111others(154): Show | 171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-111-553delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672937 | ||||||
chr11:8672937
|
CTT | C | 27 | a0001c0001t0010g0045a0002c0002t0002g0049a0002c0002t0002g0163others(24): Show | 27 | HG01167.hp1 HG01169.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.-111-554_-111-553d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672937 | ||||||
chr11:8672974
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-111-589G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672974 | ||||||
chr11:8673095
|
G | A | 2 | a0013c0013t0017g0130a0013c0013t0046g0052 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-111-710C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673095 | ||||||
chr11:8673166
|
G | A | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-111-781C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673166 | ||||||
chr11:8673179
|
C | T | 84 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(81): Show | 90 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-111-794G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673179 | ||||||
chr11:8673210
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-111-825C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673210 | ||||||
chr11:8673218
|
G | A | 1 | a0004c0021t0039g0318 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-111-833C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673218 | ||||||
chr11:8673283
|
G | A | 142 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(139): Show | 155 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-111-898C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673283 | ||||||
chr11:8673335
|
T | C | 8 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0276others(5): Show | 11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-111-950A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673335 | ||||||
chr11:8673452
|
C | A | 14 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(11): Show | 16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.-111-1067G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673452 | ||||||
chr11:8673499
|
T | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0116a0001c0001t0001g0117others(19): Show | 23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.-111-1114A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673499 | ||||||
chr11:8673586
|
T | C | 4 | a0002c0002t0002g0193a0003c0003t0003g0187a0003c0003t0003g0188others(1): Show | 4 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-1201A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673586 | ||||||
chr11:8673664
|
A | G | 5 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(2): Show | 5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112+1142T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673664 | ||||||
chr11:8673679
|
T | C | 1 | a0011c0011t0027g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-112+1127A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673679 | ||||||
chr11:8673829
|
T | C | 4 | a0004c0004t0004g0338a0004c0004t0004g0339a0004c0004t0004g0340others(1): Show | 4 | HG01071.hp2 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112+977A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673829 | ||||||
chr11:8673925
|
G | T | 6 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(3): Show | 8 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+881C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673925 | ||||||
chr11:8674140
|
G | A | 2 | a0001c0023t0004g0319a0004c0004t0004g0351 | 2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-112+666C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674140 | ||||||
chr11:8674325
|
T | C | 2 | a0018c0017t0001g0025a0018c0017t0001g0026 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-112+481A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674325 | ||||||
chr11:8674443
|
G | A | 7 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112+363C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674443 | ||||||
chr11:8674515
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-112+291G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674515 | ||||||
chr11:8674980
|
T | A | 1 | a0002c0002t0002g0279 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-189-97A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8674980 | ||||||
chr11:8675185
|
C | G | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-302G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675185 | ||||||
chr11:8675285
|
T | C | 2 | a0002c0002t0014g0286a0002c0002t0014g0287 | 2 | NA18954.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-189-402A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675285 | ||||||
chr11:8675325
|
A | T | 66 | a0001c0023t0004g0319a0004c0004t0004g0020a0004c0004t0004g0106others(63): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-189-442T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675325 | ||||||
chr11:8675458
|
T | C | 1 | a0001c0001t0022g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-189-575A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675458 | ||||||
chr11:8675469
|
ACCTCCCA others(8): Show |
A | 1 | a0001c0001t0001g0289 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-189-601_-189-587d others(17): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675469 | ||||||
chr11:8675493
|
C | T | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-610G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675493 | ||||||
chr11:8675507
|
C | T | 89 | a0002c0002t0002g0003a0002c0002t0002g0010a0002c0002t0002g0012others(86): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-189-624G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675507 | ||||||
chr11:8675642
|
A | C | 1 | a0003c0003t0006g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-189-759T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675642 | ||||||
chr11:8675680
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(126): Show | 135 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.-189-797G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675680 | ||||||
chr11:8675731
|
AATT | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0116a0001c0001t0001g0117others(19): Show | 23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.-189-851_-189-849d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675731 | ||||||
chr11:8675735
|
A | C | 1 | a0002c0002t0008g0155 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-189-852T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675735 | ||||||
chr11:8675825
|
G | A | 7 | a0008c0008t0007g0004a0008c0008t0007g0197a0008c0008t0007g0321others(4): Show | 9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189-942C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675825 | ||||||
chr11:8675927
|
C | T | 1 | a0007c0007t0026g0169 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-189-1044G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675927 | ||||||
chr11:8676234
|
CT | C | 29 | a0001c0001t0001g0168a0001c0001t0001g0198a0001c0001t0001g0223others(26): Show | 30 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-189-1352delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676234 | ||||||
chr11:8676291
|
C | T | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-1408G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676291 | ||||||
chr11:8676428
|
C | T | 1 | a0002c0002t0002g0248 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-189-1545G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676428 | ||||||
chr11:8676520
|
G | A | 4 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-1637C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676520 | ||||||
chr11:8676673
|
T | C | 2 | a0002c0002t0002g0028a0002c0002t0002g0029 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-189-1790A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676673 | ||||||
chr11:8676679
|
A | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0199 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-189-1796T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676679 | ||||||
chr11:8676709
|
C | T | 2 | a0003c0003t0003g0235a0003c0003t0003g0241 | 2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-189-1826G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676709 | ||||||
chr11:8676711
|
C | A | 5 | a0013c0013t0017g0130a0013c0013t0019g0120a0013c0013t0019g0121others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-1828G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676711 | ||||||
chr11:8676781
|
T | C | 97 | a0001c0001t0001g0122a0002c0002t0002g0003a0002c0002t0002g0010others(94): Show | 106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-189-1898A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676781 | ||||||
chr11:8676904
|
A | G | 4 | a0014c0015t0011g0075a0014c0015t0011g0076a0014c0015t0011g0077others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-2021T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676904 | ||||||
chr11:8676991
|
C | T | 1 | a0006c0006t0002g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-189-2108G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676991 | ||||||
chr11:8677194
|
A | T | 1 | a0001c0001t0001g0234 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-189-2311T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677194 | ||||||
chr11:8677353
|
A | G | 366 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(363): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.-190+2267T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677353 | ||||||
chr11:8677442
|
C | A | 1 | a0002c0002t0008g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-190+2178G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677442 | ||||||
chr11:8677469
|
T | C | 1 | a0002c0002t0002g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-190+2151A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677469 | ||||||
chr11:8677478
|
G | T | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0003c0003t0003g0073others(5): Show | 8 | HG00621.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-190+2142C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677478 | ||||||
chr11:8677572
|
A | G | 1 | a0001c0001t0037g0352 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-190+2048T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677572 | ||||||
chr11:8677624
|
CA | C | 13 | a0001c0001t0001g0072a0003c0003t0003g0129a0003c0003t0005g0208others(10): Show | 13 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190+1995delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677624 | ||||||
chr11:8677678
|
T | C | 169 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0131others(166): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.-190+1942A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677678 | ||||||
chr11:8677747
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0166a0001c0001t0001g0168others(2): Show | 7 | HG00738.hp2 HG00741.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190+1873A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677747 | ||||||
chr11:8677859
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG02922.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-190+1761G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677859 | ||||||
chr11:8678053
|
A | C | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0003c0003t0003g0232 | 3 | HG02040.hp1 HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-190+1567T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678053 | ||||||
chr11:8678115
|
A | G | 78 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0297others(75): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.-190+1505T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678115 | ||||||
chr11:8678163
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | NA18939.hp1 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-190+1457T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678163 | ||||||
chr11:8678258
|
T | TC | 4 | a0011c0011t0021g0050a0011c0011t0021g0051a0011c0011t0045g0053others(1): Show | 4 | HG02896.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1361_-190+136 others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678258 | ||||||
chr11:8678263
|
T | A | 4 | a0011c0011t0021g0050a0011c0011t0021g0051a0011c0011t0045g0053others(1): Show | 4 | HG02896.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1357A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678263 | ||||||
chr11:8678611
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0219a0001c0001t0001g0220others(17): Show | 21 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-190+1009T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678611 | ||||||
chr11:8678620
|
C | T | 208 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0023others(205): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-190+1000G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678620 | ||||||
chr11:8678737
|
T | G | 34 | a0001c0001t0001g0189a0002c0002t0002g0010a0002c0002t0002g0065others(31): Show | 37 | HG00609.hp1 HG00642.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.-190+883A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678737 | ||||||
chr11:8678779
|
T | C | 2 | a0001c0001t0001g0294a0001c0001t0015g0354 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-190+841A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678779 | ||||||
chr11:8678780
|
G | C | 72 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0233others(69): Show | 79 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-190+840C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678780 | ||||||
chr11:8678965
|
A | C | 2 | a0001c0001t0001g0233a0002c0002t0002g0288 | 2 | NA18957.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-190+655T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678965 | ||||||
chr11:8679113
|
C | A | 6 | a0006c0006t0002g0207a0012c0012t0009g0212a0012c0012t0009g0213others(3): Show | 6 | HG00639.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190+507G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679113 | ||||||
chr11:8679176
|
C | T | 1 | a0020c0038t0001g0068 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-190+444G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679176 | ||||||
chr11:8679344
|
C | T | 1 | a0004c0004t0004g0366 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-190+276G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679344 | ||||||
chr11:8679455
|
G | T | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-190+165C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679455 | ||||||
chr11:8679501
|
G | A | 1 | a0013c0013t0047g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-190+119C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679501 | ||||||
chr11:8679527
|
C | A | 4 | a0002c0002t0002g0285a0002c0002t0014g0286a0002c0002t0014g0287others(1): Show | 4 | HG02165.hp2 NA18954.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-190+93G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679527 | ||||||
chr11:8679582
|
A | G | 5 | a0011c0011t0021g0050a0011c0011t0021g0051a0011c0011t0045g0053others(2): Show | 5 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190+38T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679582 | ||||||
chr11:8680273
|
G | A | 1 | a0003c0003t0003g0048 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-547-210C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680273 | ||||||
chr11:8680289
|
C | T | 88 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0297others(85): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-547-226G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680289 | ||||||
chr11:8680330
|
G | A | 1 | a0004c0004t0033g0355 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-547-267C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680330 | ||||||
chr11:8680341
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-547-278C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680341 | ||||||
chr11:8680457
|
A | AG | 209 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0023others(206): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-547-395dupC | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680457 | ||||||
chr11:8680457
|
A | G | 1 | a0026c0036t0017g0367 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-547-394T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680457 | ||||||
chr11:8680469
|
C | T | 7 | a0006c0006t0002g0207a0012c0012t0009g0212a0012c0012t0009g0213others(4): Show | 7 | HG00639.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-547-406G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680469 | ||||||
chr11:8680489
|
T | C | 8 | a0002c0002t0002g0360a0003c0003t0003g0005a0003c0003t0003g0296others(5): Show | 10 | HG00735.hp1 HG01081.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-547-426A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680489 | ||||||
chr11:8680505
|
C | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-547-442G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680505 | ||||||
chr11:8680509
|
A | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0003c0003t0003g0232 | 3 | HG02040.hp1 HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-547-446T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680509 | ||||||
chr11:8680526
|
T | C | 3 | a0002c0002t0002g0049a0003c0003t0003g0048a0006c0006t0002g0047 | 3 | HG02451.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-547-463A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680526 | ||||||
chr11:8680595
|
C | T | 111 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0023others(108): Show | 119 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.-547-532G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680595 | ||||||
chr11:8680666
|
G | C | 3 | a0001c0001t0001g0196a0001c0001t0001g0198a0008c0008t0007g0197 | 3 | HG01168.hp1 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-547-603C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680666 | ||||||
chr11:8680682
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG01243.hp1 HG01496.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.-547-619G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680682 | ||||||
chr11:8680708
|
G | A | 1 | a0003c0003t0005g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-547-645C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680708 | ||||||
chr11:8680754
|
G | A | 1 | a0002c0002t0002g0205 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-547-691C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680754 | ||||||
chr11:8680922
|
A | G | 210 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0023others(207): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-547-859T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680922 | ||||||
chr11:8680926
|
C | G | 1 | a0001c0001t0015g0229 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-547-863G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680926 | ||||||
chr11:8681028
|
C | T | 3 | a0001c0001t0001g0196a0001c0001t0001g0198a0008c0008t0007g0197 | 3 | HG01168.hp1 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-547-965G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681028 | ||||||
chr11:8681043
|
C | T | 1 | a0009c0009t0001g0021 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-547-980G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681043 | ||||||
chr11:8681122
|
G | C | 5 | a0012c0012t0009g0212a0012c0012t0009g0213a0012c0012t0009g0214others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-547-1059C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681122 | ||||||
chr11:8681134
|
A | AT | 77 | a0001c0001t0001g0058a0001c0001t0001g0230a0001c0001t0001g0231others(74): Show | 84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-547-1072dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681134 | ||||||
chr11:8681134
|
AT | A | 11 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0199others(8): Show | 11 | HG00323.hp1 HG01168.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.-547-1072delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681134 | ||||||
chr11:8681134
|
ATT | A | 37 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(34): Show | 38 | HG00621.hp2 HG01243.hp1 HG01516.hp1 others(35): Show |
intron_variant | MODIFIER | c.-547-1073_-547-107 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681134 | ||||||
chr11:8681179
|
G | A | 11 | a0003c0003t0005g0208a0003c0003t0005g0209a0003c0003t0005g0210others(8): Show | 11 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-547-1116C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681179 | ||||||
chr11:8681184
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-547-1121T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681184 | ||||||
chr11:8681186
|
T | C | 78 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0233others(75): Show | 85 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-547-1123A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681186 | ||||||
chr11:8681262
|
T | G | 11 | a0003c0003t0005g0208a0003c0003t0005g0209a0003c0003t0005g0210others(8): Show | 11 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-547-1199A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681262 | ||||||
chr11:8681278
|
C | T | 1 | a0010c0010t0012g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-547-1215G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681278 | ||||||
chr11:8681376
|
G | A | 1 | a0004c0004t0004g0363 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-548+1225C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681376 | ||||||
chr11:8681379
|
C | A | 1 | a0001c0001t0015g0215 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-548+1222G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681379 | ||||||
chr11:8681446
|
T | C | 2 | a0002c0002t0002g0217a0003c0003t0003g0216 | 2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-548+1155A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681446 | ||||||
chr11:8681594
|
G | A | 1 | a0015c0014t0004g0364 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-548+1007C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681594 | ||||||
chr11:8681647
|
ATGC | A | 77 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0297others(74): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.-548+951_-548+953d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681647 | ||||||
chr11:8681661
|
G | A | 1 | a0008c0008t0007g0365 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-548+940C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681661 | ||||||
chr11:8681683
|
G | C | 1 | a0004c0004t0004g0366 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-548+918C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681683 | ||||||
chr11:8681884
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0219a0001c0001t0001g0220others(6): Show | 10 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-548+717A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681884 | ||||||
chr11:8681949
|
C | CGGGGGGG others(24): Show |
1 | a0003c0003t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-548+651_-548+652i others(33): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681949 | ||||||
chr11:8681951
|
A | G | 1 | a0003c0003t0003g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-548+650T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681951 | ||||||
chr11:8682055
|
C | A | 2 | a0012c0012t0009g0227a0012c0012t0009g0228 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-548+546G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682055 | ||||||
chr11:8682394
|
T | C | 111 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(108): Show | 118 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-548+207A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682394 | ||||||
chr11:8682426
|
G | GC | 75 | a0001c0001t0001g0295a0001c0001t0001g0297a0001c0001t0001g0298others(72): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.-548+174dupG | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682426 | ||||||
chr11:8682440
|
G | C | 1 | a0026c0036t0017g0367 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-548+161C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682440 | ||||||
chr11:8682459
|
T | A | 1 | a0002c0019t0030g0368 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-548+142A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682459 | ||||||
chr11:8682472
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-548+129C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682472 | ||||||
chr11:8682491
|
C | T | 5 | a0011c0011t0021g0050a0011c0011t0021g0051a0011c0011t0045g0053others(2): Show | 5 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-548+110G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682491 | ||||||
chr11:8682492
|
G | A | 32 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(29): Show | 32 | HG00621.hp2 HG01243.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-548+109C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682492 | ||||||
chr11:8682544
|
C | T | 32 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(29): Show | 32 | HG00621.hp2 HG01243.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-548+57G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682544 |