geneid | 57093 |
---|---|
ensemblid | ENSG00000168930.13 |
hgncid | 13431 |
symbol | TRIM49 |
name | tripartite motif containing 49 |
refseq_nuc | NM_020358.2 |
refseq_prot | NP_065091.1 |
ensembl_nuc | ENST00000329758.5 |
ensembl_prot | ENSP00000327604.1 |
mane_status | MANE Select |
chr | chr11 |
start | 89797655 |
end | 89808575 |
strand | - |
ver | v1.2 |
region | chr11:89797655-89808575 |
region5000 | chr11:89792655-89813575 |
regionname0 | TRIM49_chr11_89797655_89808575 |
regionname5000 | TRIM49_chr11_89792655_89813575 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 452 | 69 | 7 | 16 | 28 | 5 | 12 | 22 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0002 | 0/0 | 452 | 69 | 2 | 16 | 37 | 6 | 8 | 25 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003 | 0/0 | 452 | 49 | 16 | 9 | 18 | 1 | 5 | 12 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0004 | 0/0 | 452 | 33 | 1 | 4 | 25 | 0 | 3 | 24 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0005 | 0/0 | 452 | 11 | 0 | 0 | 7 | 0 | 4 | 7 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0006 | 0/0 | 452 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0007 | 0/0 | 452 | 4 | 0 | 0 | 0 | 2 | 2 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0008 | 0/0 | 452 | 3 | 1 | 0 | 1 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0009 | 0/0 | 452 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0010 | 0/0 | 452 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0011 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0012 | 0/0 | 452 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0013 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0014 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1359 | 69 | 2 | 16 | 37 | 6 | 8 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0002 | 1/0 | 1359 | 65 | 6 | 14 | 27 | 5 | 12 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0003 | 0/0 | 1359 | 45 | 12 | 9 | 18 | 1 | 5 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0004 | 0/0 | 1359 | 33 | 1 | 4 | 25 | 0 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0005 | 0/0 | 1359 | 11 | 0 | 0 | 7 | 0 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0006 | 0/0 | 1359 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0007 | 0/0 | 1359 | 4 | 1 | 2 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0008 | 0/0 | 1359 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0009 | 0/0 | 1359 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0010 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0011 | 0/0 | 1359 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0012 | 0/0 | 1359 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0013 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0014 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0015 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0016 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0017 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0018 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0019 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
c0020 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 805 | 134 | 7 | 30 | 64 | 11 | 21 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0002 | 0/0 | 805 | 51 | 14 | 5 | 26 | 0 | 6 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0003 | 0/0 | 805 | 22 | 0 | 7 | 13 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0004 | 0/0 | 805 | 19 | 5 | 2 | 7 | 0 | 5 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0005 | 0/0 | 805 | 6 | 4 | 1 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0006 | 0/0 | 806 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0007 | 0/0 | 805 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0008 | 0/0 | 805 | 3 | 1 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0009 | 0/0 | 805 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0010 | 0/0 | 805 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0011 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0012 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
t0013 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
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 | 35 | 1 | 9 | 18 | 4 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0002 | 1/0 | 22 | 1 | 7 | 7 | 3 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0003 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0004 | 0/0 | 8 | 1 | 0 | 2 | 1 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0008 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0009 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0011 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0013 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 1359 | 65 | 6 | 14 | 27 | 5 | 12 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0001c0007 | 0/0 | 1359 | 4 | 1 | 2 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0002c0001 | 0/0 | 1359 | 69 | 2 | 16 | 37 | 6 | 8 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0003 | 0/0 | 1359 | 45 | 12 | 9 | 18 | 1 | 5 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0009 | 0/0 | 1359 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0018 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0004c0004 | 0/0 | 1359 | 33 | 1 | 4 | 25 | 0 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0005c0005 | 0/0 | 1359 | 11 | 0 | 0 | 7 | 0 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0006c0008 | 0/0 | 1359 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0006c0013 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0006c0014 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0007c0006 | 0/0 | 1359 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0008c0012 | 0/0 | 1359 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0008c0017 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0009c0011 | 0/0 | 1359 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0010c0010 | 0/0 | 1359 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0011c0016 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0012c0015 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0013c0019 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0014c0020 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 1/0 | 2163 | 63 | 5 | 14 | 26 | 5 | 12 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0001c0002t0004 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0001c0002t0013 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0001c0007t0004 | 0/0 | 2163 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0001c0007t0009 | 0/0 | 2163 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0002c0001t0001 | 0/0 | 2163 | 68 | 2 | 16 | 37 | 6 | 7 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0002c0001t0009 | 0/0 | 2163 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0003t0002 | 0/0 | 2163 | 13 | 8 | 1 | 1 | 0 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0003t0003 | 0/0 | 2163 | 22 | 0 | 7 | 13 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0003t0005 | 0/0 | 2163 | 6 | 4 | 1 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0003t0006 | 0/0 | 2164 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0009t0002 | 0/0 | 2163 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0003c0018t0002 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0004c0004t0002 | 0/0 | 2163 | 32 | 1 | 4 | 24 | 0 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0004c0004t0012 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0005c0005t0004 | 0/0 | 2163 | 11 | 0 | 0 | 7 | 0 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0006c0008t0004 | 0/0 | 2163 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0006c0013t0010 | 0/0 | 2163 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0006c0014t0011 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0007c0006t0007 | 0/0 | 2163 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0008c0012t0008 | 0/0 | 2163 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0008c0017t0008 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0009c0011t0001 | 0/0 | 2163 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0010c0010t0006 | 0/0 | 2164 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0011c0016t0002 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0012c0015t0004 | 0/0 | 2163 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0013c0019t0001 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
a0014c0020t0002 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | copy fasta | chr11 | 89792655 | 89813575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0002 | 1/0 | 22 | 1 | 7 | 7 | 3 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0004 | 0/0 | 8 | 1 | 0 | 2 | 1 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0002t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0007t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0007t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0007t0009g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0001c0007t0009g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0001 | 0/0 | 35 | 1 | 9 | 18 | 4 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0002c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0002g0009 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0006g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0003t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0009t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0009t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0009t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0003c0018t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0003 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0004c0004t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0005c0005t0004g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0005c0005t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0005c0005t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0005c0005t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0005c0005t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0005c0005t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0006c0008t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0006c0008t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0006c0008t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0006c0008t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0006c0013t0010g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0006c0014t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0007c0006t0007g0011 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0008c0012t0008g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0008c0017t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0009c0011t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0010c0010t0006g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0011c0016t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0012c0015t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0013c0019t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
a0014c0020t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0013 | EUR | GBR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | GBR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00280 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | FIN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00408 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00408 | hp2 | a0003 | c0003 | t0006 | g0072 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00609 | hp1 | a0003 | c0003 | t0003 | g0025 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00621 | hp1 | a0003 | c0003 | t0003 | g0064 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0092 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00735 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0079 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01081 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01081 | hp2 | a0006 | c0008 | t0004 | g0113 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01099 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01099 | hp2 | a0003 | c0003 | t0002 | g0035 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01168 | hp1 | a0002 | c0001 | t0001 | g0093 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0053 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0080 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01192 | hp2 | a0003 | c0003 | t0005 | g0039 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01243 | hp2 | a0001 | c0007 | t0009 | g0107 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01257 | hp2 | a0003 | c0003 | t0003 | g0057 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01261 | hp1 | a0001 | c0007 | t0004 | g0118 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01261 | hp2 | a0002 | c0001 | t0001 | g0094 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01361 | hp2 | a0004 | c0004 | t0002 | g0024 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01433 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01433 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01496 | hp1 | a0003 | c0003 | t0003 | g0006 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01496 | hp2 | a0004 | c0004 | t0002 | g0024 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0013 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01515 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01516 | hp2 | a0007 | c0006 | t0007 | g0011 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01517 | hp1 | a0007 | c0006 | t0007 | g0011 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01884 | hp1 | a0003 | c0003 | t0002 | g0055 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0081 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01891 | hp2 | a0003 | c0003 | t0002 | g0036 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01975 | hp1 | a0003 | c0003 | t0003 | g0017 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01975 | hp2 | a0003 | c0003 | t0003 | g0066 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01981 | hp2 | a0004 | c0004 | t0002 | g0015 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01993 | hp1 | a0003 | c0003 | t0003 | g0073 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01993 | hp2 | a0003 | c0003 | t0003 | g0017 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02004 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02004 | hp2 | a0004 | c0004 | t0002 | g0052 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02015 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02040 | hp1 | a0003 | c0003 | t0003 | g0065 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02056 | hp2 | a0003 | c0003 | t0003 | g0071 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0100 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02071 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02129 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02129 | hp2 | a0008 | c0012 | t0008 | g0019 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02132 | hp2 | a0004 | c0004 | t0002 | g0046 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02135 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02135 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02293 | hp1 | a0003 | c0003 | t0003 | g0068 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02602 | hp2 | a0005 | c0005 | t0004 | g0121 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02683 | hp2 | a0005 | c0005 | t0004 | g0116 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02738 | hp2 | a0009 | c0011 | t0001 | g0029 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02809 | hp1 | a0001 | c0007 | t0004 | g0112 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02809 | hp2 | a0003 | c0009 | t0002 | g0077 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02886 | hp1 | a0003 | c0009 | t0002 | g0076 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02886 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02895 | hp1 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02895 | hp2 | a0006 | c0008 | t0004 | g0111 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02922 | hp1 | a0001 | c0002 | t0004 | g0114 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02922 | hp2 | a0006 | c0013 | t0010 | g0031 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02965 | hp1 | a0006 | c0008 | t0004 | g0109 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02965 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03017 | hp1 | a0005 | c0005 | t0004 | g0007 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0027 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03130 | hp1 | a0006 | c0014 | t0011 | g0042 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03130 | hp2 | a0014 | c0020 | t0002 | g0058 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03195 | hp1 | a0003 | c0018 | t0002 | g0043 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03195 | hp2 | a0003 | c0003 | t0005 | g0020 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03225 | hp1 | a0003 | c0003 | t0002 | g0032 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03516 | hp1 | a0003 | c0003 | t0002 | g0010 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03516 | hp2 | a0006 | c0008 | t0004 | g0110 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03654 | hp1 | a0002 | c0001 | t0001 | g0013 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03654 | hp2 | a0009 | c0011 | t0001 | g0029 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03669 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03688 | hp2 | a0008 | c0012 | t0008 | g0019 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03704 | hp1 | a0007 | c0006 | t0007 | g0011 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03710 | hp2 | a0003 | c0003 | t0002 | g0009 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03831 | hp1 | a0005 | c0005 | t0004 | g0117 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03927 | hp2 | a0004 | c0004 | t0002 | g0015 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03942 | hp2 | a0003 | c0003 | t0002 | g0009 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04115 | hp1 | a0012 | c0015 | t0004 | g0122 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04115 | hp2 | a0003 | c0003 | t0003 | g0069 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04184 | hp1 | a0003 | c0003 | t0003 | g0006 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04184 | hp2 | a0004 | c0004 | t0002 | g0003 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0085 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04199 | hp2 | a0002 | c0001 | t0009 | g0115 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0099 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG04228 | hp2 | a0003 | c0003 | t0002 | g0037 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18612 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | CHB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18939 | hp2 | a0004 | c0004 | t0002 | g0022 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18944 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18944 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18949 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18949 | hp2 | a0004 | c0004 | t0012 | g0047 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18950 | hp1 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18950 | hp2 | a0004 | c0004 | t0002 | g0050 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18953 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18953 | hp2 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18954 | hp1 | a0013 | c0019 | t0001 | g0106 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18959 | hp2 | a0003 | c0003 | t0006 | g0021 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18960 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18960 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18961 | hp1 | a0010 | c0010 | t0006 | g0026 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18964 | hp1 | a0004 | c0004 | t0002 | g0049 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18964 | hp2 | a0004 | c0004 | t0002 | g0044 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18965 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18965 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18966 | hp1 | a0003 | c0003 | t0006 | g0021 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18968 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18973 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18975 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18977 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18977 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18978 | hp2 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18980 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18981 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18981 | hp2 | a0011 | c0016 | t0002 | g0045 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18982 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18992 | hp1 | a0005 | c0005 | t0004 | g0119 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18992 | hp2 | a0004 | c0004 | t0002 | g0015 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18993 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18994 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18994 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18998 | hp2 | a0003 | c0003 | t0006 | g0074 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18999 | hp1 | a0003 | c0003 | t0003 | g0025 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19001 | hp1 | a0005 | c0005 | t0004 | g0120 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19004 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19004 | hp2 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0067 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19005 | hp2 | a0001 | c0002 | t0013 | g0075 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19007 | hp1 | a0010 | c0010 | t0006 | g0026 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19007 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19009 | hp2 | a0001 | c0007 | t0009 | g0108 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19011 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19030 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | LWK | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19030 | hp2 | a0004 | c0004 | t0002 | g0048 | AFR | LWK | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19057 | hp2 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19063 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19065 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19065 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19066 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19070 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19070 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19074 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19074 | hp2 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19076 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19077 | hp1 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19077 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0017 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19081 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19084 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19087 | hp1 | a0003 | c0003 | t0003 | g0063 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19087 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19088 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19091 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA19091 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ASW | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | ASW | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20805 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20805 | hp2 | a0003 | c0003 | t0005 | g0040 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20905 | hp1 | a0004 | c0004 | t0002 | g0051 | SAS | GIH | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20905 | hp2 | a0007 | c0006 | t0007 | g0011 | SAS | GIH | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG01123 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02486 | hp1 | a0003 | c0003 | t0005 | g0041 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02486 | hp2 | a0003 | c0009 | t0002 | g0078 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02559 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG02559 | hp2 | a0003 | c0003 | t0005 | g0038 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03471 | hp1 | a0008 | c0017 | t0008 | g0034 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
HG03471 | hp2 | a0003 | c0003 | t0005 | g0020 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18955 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA18955 | hp2 | a0004 | c0004 | t0002 | g0022 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20300 | hp1 | a0006 | c0013 | t0010 | g0031 | AFR | USA | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
NA20300 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | USA | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0002 | REF | REF | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:89798152
|
A | T | 1 | a0012 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1337T>A | p.Ile446Asn | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1666/2163 | 1337/1359 | 446/452 | chr11 | 89798152 | ||
chr11:89798308
|
G | T | 2 | a0004a0011 | 34 | HG01361.hp2 HG01496.hp2 HG01981.hp2 others(31): Show |
missense_variant | MODERATE | c.1181C>A | p.Thr394Asn | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1510/2163 | 1181/1359 | 394/452 | chr11 | 89798308 | ||
chr11:89798342
|
C | T | 6 | a0003a0004a0006others(3): Show | 93 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
missense_variant | MODERATE | c.1147G>A | p.Val383Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1476/2163 | 1147/1359 | 383/452 | chr11 | 89798342 | ||
chr11:89798365
|
G | T | 6 | a0003a0004a0006others(3): Show | 93 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
missense_variant | MODERATE | c.1124C>A | p.Ala375Glu | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1453/2163 | 1124/1359 | 375/452 | chr11 | 89798365 | ||
chr11:89798372
|
C | T | 3 | a0002a0009a0013 | 72 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
missense_variant | MODERATE | c.1117G>A | p.Gly373Arg | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1446/2163 | 1117/1359 | 373/452 | chr11 | 89798372 | ||
chr11:89798596
|
T | C | 7 | a0003a0004a0006others(4): Show | 96 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(93): Show |
missense_variant | MODERATE | c.893A>G | p.Asn298Ser | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1222/2163 | 893/1359 | 298/452 | chr11 | 89798596 | ||
chr11:89798612
|
G | C | 5 | a0003a0004a0010others(2): Show | 86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
missense_variant | MODERATE | c.877C>G | p.His293Asp | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1206/2163 | 877/1359 | 293/452 | chr11 | 89798612 | ||
chr11:89801771
|
C | T | 1 | a0009 | 2 | HG02738.hp2 HG03654.hp2 |
missense_variant | MODERATE | c.669G>A | p.Met223Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/8 | 998/2163 | 669/1359 | 223/452 | chr11 | 89801771 | ||
chr11:89803741
|
T | C | 1 | a0013 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.464A>G | p.His155Arg | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/8 | 793/2163 | 464/1359 | 155/452 | chr11 | 89803741 | ||
chr11:89803762
|
C | A | 2 | a0005a0012 | 12 | HG02602.hp2 HG02683.hp2 HG03017.hp1 others(9): Show |
missense_variant | MODERATE | c.443G>T | p.Trp148Leu | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/8 | 772/2163 | 443/1359 | 148/452 | chr11 | 89803762 | ||
chr11:89804151
|
C | G | 1 | a0010 | 2 | NA18961.hp1 NA19007.hp1 |
missense_variant | MODERATE | c.319G>C | p.Asp107His | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 648/2163 | 319/1359 | 107/452 | chr11 | 89804151 | ||
chr11:89804164
|
T | C | 1 | a0014 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.306A>G | p.Ile102Met | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 635/2163 | 306/1359 | 102/452 | chr11 | 89804164 | ||
chr11:89804231
|
A | G | 1 | a0011 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.239T>C | p.Val80Ala | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 568/2163 | 239/1359 | 80/452 | chr11 | 89804231 | ||
chr11:89804285
|
A | C | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.185T>G | p.Ile62Arg | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 514/2163 | 185/1359 | 62/452 | chr11 | 89804285 | ||
chr11:89804291
|
T | C | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.179A>G | p.Glu60Gly | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 508/2163 | 179/1359 | 60/452 | chr11 | 89804291 | ||
chr11:89804292
|
C | A | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
stop_gained | HIGH | c.178G>T | p.Glu60* | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 507/2163 | 178/1359 | 60/452 | chr11 | 89804292 | ||
chr11:89804298
|
A | T | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.172T>A | p.Ser58Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 501/2163 | 172/1359 | 58/452 | chr11 | 89804298 | ||
chr11:89804303
|
G | A | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.167C>T | p.Thr56Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 496/2163 | 167/1359 | 56/452 | chr11 | 89804303 | ||
chr11:89804312
|
G | A | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.158C>T | p.Ser53Phe | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 487/2163 | 158/1359 | 53/452 | chr11 | 89804312 | ||
chr11:89804321
|
A | G | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.149T>C | p.Val50Ala | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 478/2163 | 149/1359 | 50/452 | chr11 | 89804321 | ||
chr11:89804322
|
C | T | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.148G>A | p.Val50Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 477/2163 | 148/1359 | 50/452 | chr11 | 89804322 | ||
chr11:89804328
|
A | T | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.142T>A | p.Phe48Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 471/2163 | 142/1359 | 48/452 | chr11 | 89804328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:89798400
|
T | C | 2 | a0006c0008a0006c0013 | 6 | HG01081.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.1089A>G | p.Lys363Lys | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1418/2163 | 1089/1359 | 363/452 | chr11 | 89798400 | ||
chr11:89798451
|
A | G | 6 | a0003c0003a0003c0009a0004c0004others(3): Show | 86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
synonymous_variant | LOW | c.1038T>C | p.His346His | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1367/2163 | 1038/1359 | 346/452 | chr11 | 89798451 | ||
chr11:89804167
|
C | T | 1 | a0003c0009 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.303G>A | p.Lys101Lys | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 632/2163 | 303/1359 | 101/452 | chr11 | 89804167 | ||
chr11:89804272
|
G | A | 1 | a0007c0006 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.198C>T | p.Thr66Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 527/2163 | 198/1359 | 66/452 | chr11 | 89804272 | ||
chr11:89804293
|
G | T | 6 | a0001c0007a0005c0005a0006c0008others(3): Show | 25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
synonymous_variant | LOW | c.177C>A | p.Thr59Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 506/2163 | 177/1359 | 59/452 | chr11 | 89804293 | ||
chr11:89804302
|
T | C | 1 | a0007c0006 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.168A>G | p.Thr56Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 497/2163 | 168/1359 | 56/452 | chr11 | 89804302 | ||
chr11:89804320
|
G | A | 1 | a0007c0006 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.150C>T | p.Val50Val | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 479/2163 | 150/1359 | 50/452 | chr11 | 89804320 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:89797665
|
A | C | 11 | a0003c0003t0002a0003c0003t0003a0003c0003t0005others(8): Show | 86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*465T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 465 | chr11 | 89797665 | |||||
chr11:89797673
|
A | T | 1 | a0003c0003t0003 | 22 | HG00609.hp1 HG00621.hp1 HG01257.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*457T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 457 | chr11 | 89797673 | |||||
chr11:89797748
|
T | C | 11 | a0003c0003t0002a0003c0003t0003a0003c0003t0005others(8): Show | 86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*382A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 382 | chr11 | 89797748 | |||||
chr11:89797791
|
G | A | 1 | a0006c0013t0010 | 2 | HG02922.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*339C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 339 | chr11 | 89797791 | |||||
chr11:89797795
|
G | C | 11 | a0003c0003t0002a0003c0003t0003a0003c0003t0005others(8): Show | 87 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*335C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 335 | chr11 | 89797795 | |||||
chr11:89797795
|
G | T | 1 | a0004c0004t0012 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 335 | chr11 | 89797795 | |||||
chr11:89797830
|
T | A | 11 | a0003c0003t0002a0003c0003t0003a0003c0003t0005others(8): Show | 86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*300A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 300 | chr11 | 89797830 | |||||
chr11:89797869
|
G | GA | 2 | a0003c0003t0006a0010c0010t0006 | 6 | HG00408.hp2 NA18959.hp2 NA18961.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*260dupT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 260 | chr11 | 89797869 | |||||
chr11:89798047
|
T | C | 2 | a0008c0012t0008a0008c0017t0008 | 3 | HG02129.hp2 HG03471.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*83A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 83 | chr11 | 89798047 | |||||
chr11:89807166
|
A | G | 5 | a0001c0007t0009a0002c0001t0009a0003c0003t0005others(2): Show | 12 | HG01192.hp2 HG01243.hp2 HG02486.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-72T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/8 | 2697 | chr11 | 89807166 | |||||
chr11:89807169
|
A | G | 1 | a0007c0006t0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-75T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/8 | 2700 | chr11 | 89807169 | |||||
chr11:89807206
|
G | A | 1 | a0001c0002t0013 | 1 | NA19005.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/8 | 2737 | chr11 | 89807206 | |||||
chr11:89808448
|
A | G | 8 | a0001c0002t0004a0001c0007t0004a0001c0007t0009others(5): Show | 24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-202T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/8 | 3979 | chr11 | 89808448 | |||||
chr11:89808450
|
C | A | 1 | a0006c0013t0010 | 2 | HG02922.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-204G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/8 | 3981 | chr11 | 89808450 | |||||
chr11:89808486
|
T | C | 8 | a0001c0002t0004a0001c0007t0004a0001c0007t0009others(5): Show | 24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-240A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/8 | 4017 | chr11 | 89808486 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:89798633
|
C | CA | 39 | a0001c0002t0001g0095a0001c0007t0009g0107a0001c0007t0009g0108others(36): Show | 62 | HG01081.hp2 HG01099.hp2 HG01192.hp2 others(59): Show |
splice_region_variant&intron_variant | LOW | c.860-5dupT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798633 | ||||||
chr11:89798633
|
C | CAA | 14 | a0001c0002t0001g0023a0001c0007t0004g0112a0001c0007t0004g0118others(11): Show | 26 | HG00408.hp2 HG01261.hp1 HG02293.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.860-6_860-5dupTT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798633 | ||||||
chr11:89798633
|
C | CAAA | 7 | a0001c0002t0001g0005a0001c0002t0001g0056a0001c0002t0001g0059others(4): Show | 13 | HG00544.hp2 HG01257.hp1 HG02132.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.860-7_860-5dupTTT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798633 | ||||||
chr11:89798673
|
A | G | 1 | a0014c0020t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.860-44T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798673 | ||||||
chr11:89798735
|
T | A | 69 | a0001c0007t0004g0118a0001c0007t0009g0107a0001c0007t0009g0108others(66): Show | 115 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.860-106A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798735 | ||||||
chr11:89798813
|
A | G | 1 | a0003c0018t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.860-184T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798813 | ||||||
chr11:89798818
|
G | GT | 5 | a0003c0009t0002g0076a0003c0009t0002g0077a0003c0009t0002g0078others(2): Show | 5 | HG02132.hp2 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-190dupA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798818 | ||||||
chr11:89798818
|
G | GTT | 46 | a0003c0003t0002g0009a0003c0003t0002g0010a0003c0003t0002g0032others(43): Show | 82 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.860-191_860-190dup others(2): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798818 | ||||||
chr11:89798818
|
GT | G | 7 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0056others(4): Show | 14 | HG00544.hp2 HG01257.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.860-190delA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798818 | ||||||
chr11:89799039
|
A | G | 32 | a0003c0003t0002g0009a0003c0003t0002g0010a0003c0003t0002g0035others(29): Show | 61 | HG00408.hp2 HG01099.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.860-410T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799039 | ||||||
chr11:89799050
|
T | C | 3 | a0003c0009t0002g0076a0003c0009t0002g0077a0003c0009t0002g0078 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.860-421A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799050 | ||||||
chr11:89799133
|
G | T | 1 | a0010c0010t0006g0026 | 2 | NA18961.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.860-504C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799133 | ||||||
chr11:89799234
|
T | C | 27 | a0003c0003t0002g0009a0003c0003t0002g0010a0003c0003t0002g0035others(24): Show | 54 | HG01099.hp2 HG01192.hp2 HG01361.hp2 others(51): Show |
intron_variant | MODIFIER | c.859+482A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799234 | ||||||
chr11:89799290
|
A | G | 13 | a0003c0003t0003g0006a0003c0003t0003g0017a0003c0003t0003g0025others(10): Show | 21 | HG00609.hp1 HG01257.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.859+426T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799290 | ||||||
chr11:89799375
|
C | A | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+341G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799375 | ||||||
chr11:89799637
|
A | T | 1 | a0003c0018t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.859+79T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799637 | ||||||
chr11:89799675
|
T | A | 2 | a0003c0003t0003g0025a0003c0003t0003g0064 | 3 | HG00609.hp1 HG00621.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.859+41A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799675 | ||||||
chr11:89799691
|
G | A | 1 | a0001c0007t0009g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.859+25C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799691 | ||||||
chr11:89799826
|
A | G | 1 | a0002c0001t0001g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.762-13T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799826 | ||||||
chr11:89799895
|
A | T | 21 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(18): Show | 31 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.762-82T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799895 | ||||||
chr11:89799937
|
A | T | 10 | a0001c0007t0004g0112a0001c0007t0004g0118a0005c0005t0004g0007others(7): Show | 15 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.762-124T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799937 | ||||||
chr11:89799991
|
G | A | 2 | a0002c0001t0001g0013a0002c0001t0001g0053 | 5 | HG00099.hp1 HG00735.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.762-178C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799991 | ||||||
chr11:89800024
|
C | CT | 21 | a0001c0002t0001g0033a0001c0002t0001g0054a0003c0003t0003g0057others(18): Show | 40 | HG01243.hp1 HG01257.hp2 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.762-212dupA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800024 | ||||||
chr11:89800024
|
CTTT | C | 13 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(10): Show | 21 | HG01243.hp2 HG01261.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.762-214_762-212del others(3): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800024 | ||||||
chr11:89800024
|
CTTTT | C | 7 | a0001c0007t0009g0108a0002c0001t0009g0115a0006c0008t0004g0109others(4): Show | 8 | HG01081.hp2 HG02895.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.762-215_762-212del others(4): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800024 | ||||||
chr11:89800076
|
G | A | 1 | a0003c0003t0003g0071 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.762-263C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800076 | ||||||
chr11:89800154
|
C | T | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.762-341G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800154 | ||||||
chr11:89800156
|
G | T | 1 | a0005c0005t0004g0119 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.762-343C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800156 | ||||||
chr11:89800248
|
C | T | 10 | a0001c0007t0009g0107a0001c0007t0009g0108a0002c0001t0009g0115others(7): Show | 14 | HG01081.hp2 HG01243.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.762-435G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800248 | ||||||
chr11:89800302
|
G | A | 1 | a0002c0001t0001g0100 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.762-489C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800302 | ||||||
chr11:89800345
|
A | G | 18 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(15): Show | 24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.762-532T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800345 | ||||||
chr11:89800397
|
A | T | 2 | a0006c0014t0011g0042a0007c0006t0007g0011 | 5 | HG01516.hp2 HG01517.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+569T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800397 | ||||||
chr11:89800407
|
A | C | 8 | a0001c0007t0004g0118a0005c0005t0004g0007a0005c0005t0004g0116others(5): Show | 13 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.761+559T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800407 | ||||||
chr11:89800410
|
A | C | 10 | a0001c0007t0009g0107a0001c0007t0009g0108a0002c0001t0009g0115others(7): Show | 14 | HG01081.hp2 HG01243.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.761+556T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800410 | ||||||
chr11:89800414
|
A | ACT | 10 | a0001c0007t0009g0107a0001c0007t0009g0108a0002c0001t0009g0115others(7): Show | 14 | HG01081.hp2 HG01243.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.761+550_761+551dup others(2): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800414 | ||||||
chr11:89800414
|
A | C | 1 | a0002c0001t0001g0084 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.761+552T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800414 | ||||||
chr11:89800430
|
T | G | 2 | a0006c0014t0011g0042a0007c0006t0007g0011 | 5 | HG01516.hp2 HG01517.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+536A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800430 | ||||||
chr11:89800446
|
A | G | 1 | a0006c0014t0011g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.761+520T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800446 | ||||||
chr11:89800470
|
G | A | 19 | a0001c0002t0001g0082a0001c0007t0004g0112a0001c0007t0004g0118others(16): Show | 25 | HG00741.hp1 HG01081.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.761+496C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800470 | ||||||
chr11:89800545
|
C | G | 1 | a0003c0003t0003g0070 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.761+421G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800545 | ||||||
chr11:89800612
|
G | A | 2 | a0006c0014t0011g0042a0007c0006t0007g0011 | 5 | HG01516.hp2 HG01517.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+354C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800612 | ||||||
chr11:89800636
|
G | A | 1 | a0006c0014t0011g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.761+330C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800636 | ||||||
chr11:89800682
|
T | G | 50 | a0001c0002t0001g0103a0001c0007t0004g0118a0001c0007t0009g0107others(47): Show | 106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.761+284A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800682 | ||||||
chr11:89800736
|
C | G | 1 | a0002c0001t0009g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.761+230G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800736 | ||||||
chr11:89800742
|
CA | C | 20 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(17): Show | 29 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.761+223delT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800742 | ||||||
chr11:89800758
|
G | C | 14 | a0001c0007t0004g0112a0001c0007t0004g0118a0002c0001t0009g0115others(11): Show | 19 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.761+208C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800758 | ||||||
chr11:89800842
|
G | C | 1 | a0001c0007t0009g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.761+124C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800842 | ||||||
chr11:89800871
|
A | G | 1 | a0005c0005t0004g0121 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.761+95T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800871 | ||||||
chr11:89800921
|
G | A | 1 | a0002c0001t0001g0087 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.761+45C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800921 | ||||||
chr11:89800991
|
G | GA | 3 | a0001c0007t0009g0107a0002c0001t0001g0014a0003c0003t0005g0020 | 7 | HG01243.hp2 HG03195.hp2 HG03471.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.739-4dupT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89800991 | ||||||
chr11:89800991
|
GA | G | 9 | a0001c0007t0004g0112a0001c0007t0004g0118a0003c0003t0002g0035others(6): Show | 16 | HG01099.hp2 HG01261.hp1 HG02602.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.739-4delT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89800991 | ||||||
chr11:89800991
|
GAA | G | 3 | a0005c0005t0004g0119a0005c0005t0004g0120a0007c0006t0007g0011 | 6 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.739-5_739-4delTT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89800991 | ||||||
chr11:89801023
|
T | G | 11 | a0001c0007t0004g0112a0001c0007t0004g0118a0005c0005t0004g0007others(8): Show | 19 | HG01261.hp1 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.739-35A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801023 | ||||||
chr11:89801123
|
G | A | 19 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(16): Show | 28 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.739-135C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801123 | ||||||
chr11:89801136
|
A | T | 19 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(16): Show | 28 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.739-148T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801136 | ||||||
chr11:89801204
|
T | C | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-216A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801204 | ||||||
chr11:89801285
|
T | G | 1 | a0001c0007t0009g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.739-297A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801285 | ||||||
chr11:89801391
|
A | C | 1 | a0003c0009t0002g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.738+311T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801391 | ||||||
chr11:89801459
|
T | C | 31 | a0001c0002t0001g0097a0001c0007t0004g0112a0001c0007t0009g0107others(28): Show | 58 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.738+243A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801459 | ||||||
chr11:89801526
|
G | C | 10 | a0001c0007t0009g0108a0002c0001t0001g0088a0002c0001t0009g0115others(7): Show | 14 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.738+176C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801526 | ||||||
chr11:89801614
|
T | G | 4 | a0003c0009t0002g0076a0003c0009t0002g0077a0003c0009t0002g0078others(1): Show | 4 | HG02486.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+88A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801614 | ||||||
chr11:89802122
|
G | A | 9 | a0001c0007t0004g0112a0001c0007t0004g0118a0005c0005t0004g0007others(6): Show | 14 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-190C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802122 | ||||||
chr11:89802166
|
C | T | 10 | a0001c0007t0004g0112a0001c0007t0004g0118a0005c0005t0004g0007others(7): Show | 16 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.508-234G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802166 | ||||||
chr11:89802301
|
C | A | 18 | a0001c0002t0001g0096a0001c0007t0004g0112a0001c0007t0004g0118others(15): Show | 24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.508-369G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802301 | ||||||
chr11:89802405
|
T | G | 12 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(9): Show | 18 | HG01243.hp2 HG01261.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.508-473A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802405 | ||||||
chr11:89802491
|
T | C | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.508-559A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802491 | ||||||
chr11:89802536
|
G | A | 18 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(15): Show | 27 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.508-604C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802536 | ||||||
chr11:89802541
|
C | G | 1 | a0001c0002t0001g0102 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.508-609G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802541 | ||||||
chr11:89802568
|
T | A | 1 | a0012c0015t0004g0122 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.508-636A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802568 | ||||||
chr11:89802570
|
C | T | 1 | a0004c0004t0002g0046 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.508-638G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802570 | ||||||
chr11:89802580
|
CACAT | C | 34 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0056others(31): Show | 53 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-652_508-649del others(4): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802580 | ||||||
chr11:89802580
|
CACATACA others(1): Show |
C | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.508-656_508-649del others(8): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802580 | ||||||
chr11:89802588
|
T | C | 1 | a0006c0013t0010g0031 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.508-656A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802588 | ||||||
chr11:89802671
|
C | T | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-739G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802671 | ||||||
chr11:89802699
|
C | G | 14 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(11): Show | 19 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.508-767G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802699 | ||||||
chr11:89802750
|
C | T | 2 | a0006c0008t0004g0109a0006c0008t0004g0111 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.508-818G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802750 | ||||||
chr11:89802829
|
C | G | 2 | a0003c0009t0002g0076a0003c0009t0002g0078 | 2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.507+869G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802829 | ||||||
chr11:89802883
|
A | C | 20 | a0001c0002t0001g0008a0001c0002t0001g0082a0001c0007t0004g0112others(17): Show | 33 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.507+815T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802883 | ||||||
chr11:89802906
|
G | A | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+792C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802906 | ||||||
chr11:89802999
|
T | G | 1 | a0006c0014t0011g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.507+699A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802999 | ||||||
chr11:89803019
|
G | A | 3 | a0003c0009t0002g0076a0003c0009t0002g0077a0003c0009t0002g0078 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.507+679C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803019 | ||||||
chr11:89803048
|
G | A | 18 | a0001c0002t0001g0030a0001c0007t0004g0112a0001c0007t0004g0118others(15): Show | 28 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.507+650C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803048 | ||||||
chr11:89803090
|
T | G | 1 | a0002c0001t0001g0093 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.507+608A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803090 | ||||||
chr11:89803110
|
A | C | 3 | a0003c0003t0006g0021a0003c0003t0006g0074a0003c0018t0002g0043 | 4 | HG03195.hp1 NA18959.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+588T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803110 | ||||||
chr11:89803160
|
G | A | 1 | a0002c0001t0001g0089 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.507+538C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803160 | ||||||
chr11:89803171
|
C | T | 1 | a0002c0001t0001g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.507+527G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803171 | ||||||
chr11:89803184
|
G | A | 27 | a0001c0002t0001g0062a0002c0001t0001g0001a0002c0001t0001g0013others(24): Show | 72 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.507+514C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803184 | ||||||
chr11:89803237
|
T | C | 1 | a0006c0013t0010g0031 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.507+461A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803237 | ||||||
chr11:89803374
|
C | G | 1 | a0003c0009t0002g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+324G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803374 | ||||||
chr11:89803385
|
G | A | 3 | a0003c0009t0002g0076a0003c0009t0002g0077a0003c0009t0002g0078 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.507+313C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803385 | ||||||
chr11:89803398
|
C | T | 1 | a0003c0009t0002g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+300G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803398 | ||||||
chr11:89803540
|
A | G | 6 | a0001c0002t0001g0060a0002c0001t0009g0115a0006c0008t0004g0109others(3): Show | 6 | HG01081.hp2 HG02132.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+158T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803540 | ||||||
chr11:89803563
|
C | T | 3 | a0001c0007t0009g0107a0001c0007t0009g0108a0006c0013t0010g0031 | 4 | HG01243.hp2 HG02922.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+135G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803563 | ||||||
chr11:89803567
|
G | A | 6 | a0002c0001t0009g0115a0006c0008t0004g0109a0006c0008t0004g0110others(3): Show | 9 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+131C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803567 | ||||||
chr11:89803578
|
C | T | 2 | a0006c0008t0004g0109a0006c0008t0004g0111 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.507+120G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803578 | ||||||
chr11:89803847
|
G | C | 1 | a0002c0001t0001g0090 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.412-54C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803847 | ||||||
chr11:89803871
|
C | A | 2 | a0004c0004t0002g0044a0004c0004t0002g0050 | 2 | NA18950.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.412-78G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803871 | ||||||
chr11:89803982
|
T | C | 1 | a0002c0001t0009g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.411+77A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803982 | ||||||
chr11:89803984
|
C | T | 6 | a0002c0001t0009g0115a0006c0008t0004g0109a0006c0008t0004g0110others(3): Show | 9 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+75G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803984 | ||||||
chr11:89804021
|
T | C | 12 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0056others(9): Show | 21 | HG00544.hp2 HG00621.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.411+38A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89804021 | ||||||
chr11:89804036
|
C | A | 1 | a0002c0001t0001g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.411+23G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89804036 | ||||||
chr11:89804489
|
A | C | 12 | a0001c0002t0001g0081a0001c0007t0004g0112a0001c0007t0004g0118others(9): Show | 17 | HG01261.hp1 HG01884.hp2 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.-4-16T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804489 | ||||||
chr11:89804523
|
C | G | 70 | a0001c0002t0001g0033a0001c0002t0001g0054a0001c0002t0001g0056others(67): Show | 112 | HG00408.hp2 HG00609.hp1 HG01081.hp2 others(109): Show |
intron_variant | MODIFIER | c.-4-50G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804523 | ||||||
chr11:89804538
|
G | C | 11 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(8): Show | 16 | HG01243.hp2 HG01261.hp1 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4-65C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804538 | ||||||
chr11:89804617
|
A | G | 1 | a0014c0020t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-4-144T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804617 | ||||||
chr11:89804651
|
C | A | 16 | a0001c0007t0009g0107a0002c0001t0009g0115a0003c0003t0003g0006others(13): Show | 22 | HG00609.hp1 HG01081.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-4-178G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804651 | ||||||
chr11:89804669
|
C | T | 10 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0108others(7): Show | 15 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.-4-196G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804669 | ||||||
chr11:89804695
|
C | T | 1 | a0005c0005t0004g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4-222G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804695 | ||||||
chr11:89804713
|
A | G | 2 | a0006c0008t0004g0109a0006c0008t0004g0111 | 2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-4-240T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804713 | ||||||
chr11:89804718
|
A | G | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-245T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804718 | ||||||
chr11:89804746
|
A | G | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-273T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804746 | ||||||
chr11:89804829
|
A | G | 1 | a0005c0005t0004g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-4-356T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804829 | ||||||
chr11:89804862
|
C | T | 14 | a0001c0007t0004g0112a0001c0007t0004g0118a0002c0001t0009g0115others(11): Show | 19 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.-4-389G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804862 | ||||||
chr11:89804865
|
G | A | 14 | a0001c0007t0004g0112a0001c0007t0004g0118a0002c0001t0009g0115others(11): Show | 19 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.-4-392C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804865 | ||||||
chr11:89804865
|
GGGCCAAA others(15): Show |
G | 1 | a0003c0003t0005g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4-414_-4-393delAT others(20): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804865 | ||||||
chr11:89804935
|
A | G | 45 | a0001c0002t0001g0097a0001c0007t0004g0112a0001c0007t0004g0118others(42): Show | 76 | HG01081.hp2 HG01099.hp2 HG01192.hp2 others(73): Show |
intron_variant | MODIFIER | c.-4-462T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804935 | ||||||
chr11:89804950
|
G | A | 1 | a0001c0007t0009g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-477C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804950 | ||||||
chr11:89804967
|
C | T | 1 | a0001c0007t0009g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-494G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804967 | ||||||
chr11:89804977
|
C | T | 16 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(13): Show | 21 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.-4-504G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804977 | ||||||
chr11:89805066
|
T | A | 49 | a0001c0002t0001g0033a0001c0002t0001g0054a0001c0002t0001g0056others(46): Show | 84 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(81): Show |
intron_variant | MODIFIER | c.-4-593A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805066 | ||||||
chr11:89805117
|
T | C | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.-4-644A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805117 | ||||||
chr11:89805182
|
C | T | 1 | a0001c0007t0009g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-709G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805182 | ||||||
chr11:89805273
|
C | A | 1 | a0014c0020t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-4-800G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805273 | ||||||
chr11:89805289
|
A | G | 10 | a0001c0002t0001g0056a0003c0003t0003g0006a0003c0003t0003g0025others(7): Show | 16 | HG00609.hp1 HG01257.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4-816T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805289 | ||||||
chr11:89805395
|
C | T | 13 | a0001c0007t0004g0112a0001c0007t0004g0118a0005c0005t0004g0007others(10): Show | 18 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4-922G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805395 | ||||||
chr11:89805458
|
C | T | 1 | a0002c0001t0001g0080 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-4-985G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805458 | ||||||
chr11:89805477
|
G | T | 1 | a0001c0002t0001g0059 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-4-1004C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805477 | ||||||
chr11:89805517
|
T | A | 1 | a0003c0003t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-1044A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805517 | ||||||
chr11:89805517
|
T | C | 13 | a0001c0007t0004g0112a0001c0007t0004g0118a0005c0005t0004g0007others(10): Show | 18 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4-1044A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805517 | ||||||
chr11:89805526
|
C | G | 11 | a0001c0007t0009g0107a0001c0007t0009g0108a0002c0001t0001g0079others(8): Show | 16 | HG00639.hp1 HG00741.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4-1053G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805526 | ||||||
chr11:89805556
|
G | A | 2 | a0004c0004t0002g0051a0004c0004t0002g0052 | 2 | HG02004.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-4-1083C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805556 | ||||||
chr11:89805613
|
A | C | 1 | a0003c0003t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-1140T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805613 | ||||||
chr11:89805639
|
A | G | 2 | a0001c0002t0001g0033a0001c0002t0001g0054 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-4-1166T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805639 | ||||||
chr11:89805697
|
G | A | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-1224C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805697 | ||||||
chr11:89805723
|
G | T | 20 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(17): Show | 27 | HG00639.hp1 HG01081.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-4-1250C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805723 | ||||||
chr11:89805723
|
GT | G | 51 | a0001c0002t0001g0033a0001c0002t0001g0054a0001c0002t0001g0056others(48): Show | 86 | HG00408.hp2 HG00609.hp1 HG01099.hp2 others(83): Show |
intron_variant | MODIFIER | c.-4-1251delA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805723 | ||||||
chr11:89805724
|
T | G | 15 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(12): Show | 21 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.-4-1251A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805724 | ||||||
chr11:89805724
|
T | TG | 4 | a0002c0001t0001g0092a0002c0001t0001g0093a0002c0001t0009g0115others(1): Show | 5 | HG00639.hp1 HG01168.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-1252_-4-1251ins others(1): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805724 | ||||||
chr11:89805909
|
G | C | 1 | a0006c0013t0010g0031 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-5+1190C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805909 | ||||||
chr11:89805947
|
T | G | 16 | a0001c0002t0001g0056a0003c0003t0003g0006a0003c0003t0003g0025others(13): Show | 24 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-5+1152A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805947 | ||||||
chr11:89805994
|
C | A | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+1105G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805994 | ||||||
chr11:89806020
|
C | A | 19 | a0001c0002t0001g0098a0001c0007t0004g0112a0001c0007t0004g0118others(16): Show | 25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.-5+1079G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806020 | ||||||
chr11:89806221
|
A | G | 18 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(15): Show | 24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-5+878T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806221 | ||||||
chr11:89806261
|
C | A | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+838G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806261 | ||||||
chr11:89806268
|
G | C | 1 | a0003c0003t0002g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5+831C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806268 | ||||||
chr11:89806273
|
T | C | 19 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(16): Show | 26 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-5+826A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806273 | ||||||
chr11:89806339
|
T | C | 2 | a0003c0003t0006g0074a0003c0018t0002g0043 | 2 | HG03195.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-5+760A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806339 | ||||||
chr11:89806542
|
C | T | 1 | a0003c0009t0002g0076 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-5+557G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806542 | ||||||
chr11:89806575
|
T | A | 21 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(18): Show | 30 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-5+524A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806575 | ||||||
chr11:89806629
|
A | G | 3 | a0003c0003t0002g0032a0003c0003t0006g0021a0003c0018t0002g0043 | 4 | HG03195.hp1 HG03225.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+470T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806629 | ||||||
chr11:89806637
|
T | C | 7 | a0001c0002t0001g0004a0001c0002t0001g0030a0001c0002t0001g0095others(4): Show | 15 | HG00280.hp2 HG00544.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.-5+462A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806637 | ||||||
chr11:89806652
|
A | G | 14 | a0004c0004t0002g0003a0004c0004t0002g0012a0004c0004t0002g0015others(11): Show | 32 | HG01981.hp2 HG02004.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.-5+447T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806652 | ||||||
chr11:89806656
|
T | C | 1 | a0014c0020t0002g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+443A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806656 | ||||||
chr11:89806735
|
C | A | 1 | a0003c0003t0002g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-5+364G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806735 | ||||||
chr11:89806832
|
A | G | 2 | a0003c0003t0006g0021a0003c0018t0002g0043 | 3 | HG03195.hp1 NA18959.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-5+267T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806832 | ||||||
chr11:89806887
|
A | G | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+212T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806887 | ||||||
chr11:89806896
|
G | T | 1 | a0001c0007t0004g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-5+203C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806896 | ||||||
chr11:89806932
|
C | A | 1 | a0006c0008t0004g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5+167G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806932 | ||||||
chr11:89807016
|
C | A | 38 | a0001c0002t0001g0005a0001c0002t0001g0059a0001c0002t0001g0060others(35): Show | 59 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-5+83G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89807016 | ||||||
chr11:89807057
|
T | G | 1 | a0001c0007t0009g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-5+42A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89807057 | ||||||
chr11:89807359
|
A | G | 7 | a0003c0003t0002g0009a0003c0003t0002g0010a0003c0003t0002g0035others(4): Show | 14 | HG01099.hp2 HG01891.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-190-75T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807359 | ||||||
chr11:89807430
|
C | T | 1 | a0001c0002t0004g0114 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-190-146G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807430 | ||||||
chr11:89807443
|
T | C | 16 | a0001c0002t0001g0033a0001c0007t0004g0112a0001c0007t0004g0118others(13): Show | 21 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.-190-159A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807443 | ||||||
chr11:89807460
|
G | C | 1 | a0001c0007t0009g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-190-176C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807460 | ||||||
chr11:89807560
|
A | T | 1 | a0002c0001t0001g0104 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-190-276T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807560 | ||||||
chr11:89807663
|
C | A | 17 | a0001c0007t0004g0112a0001c0007t0004g0118a0001c0007t0009g0107others(14): Show | 23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-379G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807663 | ||||||
chr11:89807686
|
A | T | 4 | a0006c0008t0004g0109a0006c0008t0004g0110a0006c0008t0004g0111others(1): Show | 4 | HG01081.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-190-402T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807686 | ||||||
chr11:89807721
|
A | C | 14 | a0001c0002t0001g0033a0001c0007t0004g0112a0001c0007t0004g0118others(11): Show | 19 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(16): Show |
intron_variant | MODIFIER | c.-190-437T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807721 | ||||||
chr11:89807758
|
A | G | 17 | a0001c0002t0004g0114a0001c0007t0004g0112a0001c0007t0004g0118others(14): Show | 23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-474T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807758 | ||||||
chr11:89807940
|
T | C | 3 | a0003c0009t0002g0076a0003c0009t0002g0077a0003c0009t0002g0078 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-191+497A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807940 | ||||||
chr11:89808025
|
G | T | 119 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0008others(116): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-191+412C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808025 | ||||||
chr11:89808183
|
G | A | 18 | a0001c0002t0004g0114a0001c0007t0004g0112a0001c0007t0004g0118others(15): Show | 24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-191+254C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808183 | ||||||
chr11:89808204
|
A | G | 1 | a0003c0003t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+233T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808204 | ||||||
chr11:89808221
|
TA | T | 66 | a0001c0002t0001g0005a0001c0002t0001g0023a0001c0002t0001g0033others(63): Show | 113 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-191+215delT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808221 | ||||||
chr11:89808332
|
A | C | 1 | a0001c0007t0009g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-191+105T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808332 | ||||||
chr11:89808397
|
G | A | 4 | a0002c0001t0001g0018a0002c0001t0001g0104a0002c0001t0001g0105others(1): Show | 6 | HG02129.hp1 NA18612.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.-191+40C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808397 | ||||||
chr11:89808427
|
CTT | C | 8 | a0001c0007t0004g0118a0005c0005t0004g0007a0005c0005t0004g0116others(5): Show | 13 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.-191+8_-191+9delAA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808427 |