geneid | 50852 |
---|---|
ensemblid | ENSG00000163519.14 |
hgncid | 30698 |
symbol | TRAT1 |
name | T cell receptor associated transmembrane adaptor 1 |
refseq_nuc | NM_016388.4 |
refseq_prot | NP_057472.2 |
ensembl_nuc | ENST00000295756.11 |
ensembl_prot | ENSP00000295756.6 |
mane_status | MANE Select |
chr | chr3 |
start | 108822786 |
end | 108855005 |
strand | + |
ver | v1.2 |
region | chr3:108822786-108855005 |
region5000 | chr3:108817786-108860005 |
regionname0 | TRAT1_chr3_108822786_108855005 |
regionname5000 | TRAT1_chr3_108817786_108860005 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 186 | 314 | 80 | 72 | 100 | 14 | 46 | 75 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0002 | 0/0 | 186 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0003 | 0/0 | 186 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0004 | 0/0 | 186 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0005 | 0/0 | 186 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0006 | 0/0 | 186 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0007 | 0/0 | 186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0008 | 0/0 | 186 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 561 | 314 | 80 | 72 | 100 | 14 | 46 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
c0002 | 0/0 | 561 | 9 | 9 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
c0003 | 0/0 | 561 | 5 | 0 | 0 | 5 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
c0004 | 0/0 | 561 | 4 | 4 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
c0005 | 0/0 | 561 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
c0006 | 0/0 | 561 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
c0007 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
c0008 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1271 | 146 | 15 | 28 | 79 | 5 | 19 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0002 | 1/0 | 1271 | 101 | 37 | 23 | 26 | 6 | 8 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0003 | 0/0 | 1271 | 34 | 0 | 13 | 5 | 1 | 15 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0004 | 0/0 | 1271 | 23 | 19 | 4 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0005 | 0/1 | 1271 | 14 | 6 | 3 | 0 | 2 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0006 | 0/0 | 1268 | 6 | 6 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0007 | 0/0 | 1268 | 6 | 5 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0008 | 0/0 | 1271 | 4 | 4 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0009 | 0/0 | 1271 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0010 | 0/0 | 1271 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0011 | 0/0 | 1271 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0012 | 0/0 | 1271 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
t0013 | 0/0 | 1271 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
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 | 6 | 0 | 0 | 6 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0002 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0290 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 561 | 314 | 80 | 72 | 100 | 14 | 46 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0002c0002 | 0/0 | 561 | 9 | 9 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0003c0003 | 0/0 | 561 | 5 | 0 | 0 | 5 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0004c0004 | 0/0 | 561 | 4 | 4 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0005c0005 | 0/0 | 561 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0006c0006 | 0/0 | 561 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0007c0008 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0008c0007 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1831 | 139 | 15 | 28 | 72 | 5 | 19 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0002 | 1/0 | 1831 | 86 | 25 | 23 | 23 | 6 | 8 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0003 | 0/0 | 1831 | 34 | 0 | 13 | 5 | 1 | 15 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0004 | 0/0 | 1831 | 23 | 19 | 4 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0005 | 0/1 | 1831 | 14 | 6 | 3 | 0 | 2 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0006 | 0/0 | 1828 | 6 | 6 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0007 | 0/0 | 1828 | 6 | 5 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0009 | 0/0 | 1831 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0010 | 0/0 | 1831 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0011 | 0/0 | 1831 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0012 | 0/0 | 1831 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0001c0001t0013 | 0/0 | 1831 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0002c0002t0002 | 0/0 | 1831 | 9 | 9 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0003c0003t0001 | 0/0 | 1831 | 5 | 0 | 0 | 5 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0004c0004t0008 | 0/0 | 1831 | 4 | 4 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0005c0005t0002 | 0/0 | 1831 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0006c0006t0002 | 0/0 | 1831 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0007c0008t0001 | 0/0 | 1831 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
a0008c0007t0001 | 0/0 | 1831 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | copy fasta | chr3 | 108817786 | 108860005 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0290 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0006g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0007g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0010g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0011g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0012g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0001c0001t0013g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0002c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0002c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0003c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0004c0004t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0004c0004t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0004c0004t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0004c0004t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0005c0005t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0005c0005t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0006c0006t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0006c0006t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0006c0006t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0007c0008t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
a0008c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0283 | EUR | GBR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | FIN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0296 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01074 | hp2 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0223 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0185 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0292 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0224 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0284 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0263 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02055 | hp2 | a0004 | c0004 | t0008 | g0038 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02257 | hp1 | a0004 | c0004 | t0008 | g0037 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02258 | hp1 | a0005 | c0005 | t0002 | g0016 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02451 | hp2 | a0005 | c0005 | t0002 | g0016 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0107 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0208 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0126 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0267 | AFR | GWD | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0289 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0218 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0293 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03834 | hp1 | a0001 | c0001 | t0011 | g0211 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0276 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | BEB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0273 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18948 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18964 | hp2 | a0007 | c0008 | t0001 | g0237 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18966 | hp1 | a0006 | c0006 | t0002 | g0235 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0097 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18999 | hp1 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19004 | hp1 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19011 | hp1 | a0006 | c0006 | t0002 | g0055 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19062 | hp1 | a0008 | c0007 | t0001 | g0076 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19091 | hp2 | a0006 | c0006 | t0002 | g0246 | EAS | JPT | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19240 | hp1 | a0005 | c0005 | t0002 | g0141 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA19240 | hp2 | a0004 | c0004 | t0008 | g0051 | AFR | YRI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ASW | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20129 | hp2 | a0001 | c0001 | t0013 | g0122 | AFR | ASW | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0279 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0153 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0184 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | TSI | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | GIH | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | GIH | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0222 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG02559 | hp2 | a0004 | c0004 | t0008 | g0168 | AFR | ACB | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0254 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | USA | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | LWK | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0290 | REF | REF | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0035 | REF | REF | TRAT1_chr3_108817786_108860005 | TRAT1 | chr3 | 108817786 | 108860005 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:108830780
|
G | A | 1 | a0008 | 1 | NA19062.hp1 | missense_variant&splice_region_variant | MODERATE | c.118G>A | p.Asp40Asn | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/6 | 260/1831 | 118/561 | 40/186 | chr3 | 108830780 | ||
chr3:108849207
|
C | T | 2 | a0003a0008 | 6 | HG00408.hp2 NA18948.hp1 NA18969.hp2 others(3): Show |
missense_variant | MODERATE | c.256C>T | p.Pro86Ser | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/6 | 398/1831 | 256/561 | 86/186 | chr3 | 108849207 | ||
chr3:108853677
|
C | A | 1 | a0007 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.361C>A | p.Arg121Ser | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 503/1831 | 361/561 | 121/186 | chr3 | 108853677 | ||
chr3:108853686
|
C | A | 1 | a0002 | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
missense_variant | MODERATE | c.370C>A | p.Pro124Thr | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 512/1831 | 370/561 | 124/186 | chr3 | 108853686 | ||
chr3:108853726
|
A | G | 1 | a0004 | 4 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(1): Show |
missense_variant | MODERATE | c.410A>G | p.Asp137Gly | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 552/1831 | 410/561 | 137/186 | chr3 | 108853726 | ||
chr3:108853758
|
T | C | 1 | a0005 | 3 | HG02258.hp1 HG02451.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.442T>C | p.Ser148Pro | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 584/1831 | 442/561 | 148/186 | chr3 | 108853758 | ||
chr3:108853852
|
G | T | 1 | a0006 | 3 | NA18966.hp1 NA19011.hp1 NA19091.hp2 |
missense_variant | MODERATE | c.536G>T | p.Arg179Leu | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 678/1831 | 536/561 | 179/186 | chr3 | 108853852 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:108822914
|
T | C | 4 | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(1): Show | 50 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-14T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/6 | 14 | chr3 | 108822914 | |||||
chr3:108853941
|
G | A | 1 | a0001c0001t0010 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 64 | chr3 | 108853941 | |||||
chr3:108853943
|
A | G | 1 | a0001c0001t0013 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 66 | chr3 | 108853943 | |||||
chr3:108854291
|
T | A | 1 | a0001c0001t0009 | 2 | HG02559.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 414 | chr3 | 108854291 | |||||
chr3:108854500
|
TCTA | T | 1 | a0001c0001t0007 | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*627_*629delCTA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 627 | INFO_REALIGN_3_PRIME | chr3 | 108854500 | ||||
chr3:108854565
|
A | C | 1 | a0001c0001t0011 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*688A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 688 | chr3 | 108854565 | |||||
chr3:108854787
|
T | A | 1 | a0001c0001t0012 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 910 | chr3 | 108854787 | |||||
chr3:108854800
|
T | A | 2 | a0001c0001t0004a0001c0001t0013 | 24 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*923T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 923 | chr3 | 108854800 | |||||
chr3:108854802
|
T | C | 1 | a0004c0004t0008 | 4 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*925T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 925 | chr3 | 108854802 | |||||
chr3:108854936
|
C | T | 8 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | 191 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1059C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 1059 | chr3 | 108854936 | |||||
chr3:108854947
|
ATTG | A | 1 | a0001c0001t0006 | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1073_*1075delGTT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 6/6 | 1073 | INFO_REALIGN_3_PRIME | chr3 | 108854947 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:108823084
|
CAT | C | 140 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0024others(137): Show | 162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.7+151_7+152delAT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823084 | ||||||
chr3:108823147
|
C | T | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.7+213C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823147 | ||||||
chr3:108823270
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.7+336A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823270 | ||||||
chr3:108823337
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.7+403A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823337 | ||||||
chr3:108823514
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.7+580T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823514 | ||||||
chr3:108823650
|
T | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.7+716T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823650 | ||||||
chr3:108823656
|
C | T | 19 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0128others(16): Show | 22 | HG00735.hp1 HG02257.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+722C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823656 | ||||||
chr3:108823723
|
A | G | 3 | a0001c0001t0002g0014a0001c0001t0002g0116a0001c0001t0002g0117 | 4 | NA18939.hp2 NA18961.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+789A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823723 | ||||||
chr3:108823809
|
A | G | 1 | a0001c0001t0002g0169 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7+875A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823809 | ||||||
chr3:108823895
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.7+961C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108823895 | ||||||
chr3:108824018
|
C | T | 1 | a0004c0004t0008g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7+1084C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824018 | ||||||
chr3:108824113
|
G | A | 48 | a0001c0001t0001g0020a0001c0001t0001g0172a0001c0001t0001g0174others(45): Show | 56 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.7+1179G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824113 | ||||||
chr3:108824149
|
C | T | 9 | a0001c0001t0002g0128a0001c0001t0002g0130a0001c0001t0002g0131others(6): Show | 10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+1215C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824149 | ||||||
chr3:108824152
|
G | A | 9 | a0001c0001t0001g0221a0001c0001t0002g0217a0001c0001t0002g0220others(6): Show | 9 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+1218G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824152 | ||||||
chr3:108824303
|
A | T | 3 | a0001c0001t0004g0112a0001c0001t0004g0113a0001c0001t0004g0114 | 3 | HG01884.hp2 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.7+1369A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824303 | ||||||
chr3:108824398
|
A | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(75): Show | 90 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.7+1464A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824398 | ||||||
chr3:108824483
|
A | C | 1 | a0001c0001t0002g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+1549A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824483 | ||||||
chr3:108824528
|
G | T | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 333 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.7+1594G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108824528 | ||||||
chr3:108825124
|
TA | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0024others(139): Show | 164 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.7+2191delA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825124 | ||||||
chr3:108825128
|
T | C | 1 | a0001c0001t0002g0023 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.7+2194T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825128 | ||||||
chr3:108825278
|
C | T | 4 | a0001c0001t0006g0019a0001c0001t0006g0164a0001c0001t0006g0165others(1): Show | 5 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+2344C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825278 | ||||||
chr3:108825300
|
T | G | 3 | a0001c0001t0004g0011a0001c0001t0004g0052a0004c0004t0008g0051 | 4 | HG01069.hp2 HG01071.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2366T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825300 | ||||||
chr3:108825407
|
T | C | 1 | a0001c0001t0001g0004 | 3 | NA18943.hp2 NA18948.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.7+2473T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825407 | ||||||
chr3:108825427
|
A | T | 89 | a0001c0001t0001g0018a0001c0001t0001g0135a0001c0001t0001g0137others(86): Show | 100 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.7+2493A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825427 | ||||||
chr3:108825428
|
A | T | 1 | a0001c0001t0005g0266 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.7+2494A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825428 | ||||||
chr3:108825504
|
C | T | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 87 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.7+2570C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825504 | ||||||
chr3:108825719
|
A | T | 1 | a0001c0001t0005g0296 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7+2785A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825719 | ||||||
chr3:108825877
|
G | A | 2 | a0001c0001t0002g0268a0001c0001t0007g0267 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.7+2943G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825877 | ||||||
chr3:108825889
|
G | T | 2 | a0004c0004t0008g0037a0004c0004t0008g0038 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.7+2955G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108825889 | ||||||
chr3:108826005
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+3071A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826005 | ||||||
chr3:108826227
|
T | TCAGTGAT others(11): Show |
249 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(246): Show | 289 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.7+3296_7+3297insTG others(16): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108826227 | |||||
chr3:108826340
|
C | T | 7 | a0001c0001t0001g0264a0001c0001t0002g0260a0001c0001t0002g0261others(4): Show | 8 | HG01192.hp1 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+3406C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826340 | ||||||
chr3:108826421
|
T | C | 41 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(38): Show | 46 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.7+3487T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826421 | ||||||
chr3:108826515
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7+3581G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826515 | ||||||
chr3:108826531
|
G | A | 21 | a0001c0001t0001g0020a0001c0001t0001g0172a0001c0001t0001g0174others(18): Show | 22 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+3597G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826531 | ||||||
chr3:108826598
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.7+3664C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826598 | ||||||
chr3:108826762
|
A | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0040others(10): Show | 16 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.7+3828A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826762 | ||||||
chr3:108826816
|
G | A | 39 | a0001c0001t0001g0018a0001c0001t0001g0135a0001c0001t0001g0137others(36): Show | 43 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.8-3854G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826816 | ||||||
chr3:108826916
|
A | C | 7 | a0001c0001t0002g0217a0001c0001t0002g0220a0001c0001t0007g0218others(4): Show | 7 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-3754A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108826916 | ||||||
chr3:108827009
|
G | A | 10 | a0001c0001t0003g0207a0001c0001t0003g0209a0001c0001t0003g0210others(7): Show | 10 | HG01361.hp1 HG01934.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-3661G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827009 | ||||||
chr3:108827115
|
T | G | 221 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.8-3555T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827115 | ||||||
chr3:108827116
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.8-3554T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827116 | ||||||
chr3:108827214
|
G | T | 35 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(32): Show | 41 | HG00597.hp1 HG00639.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.8-3456G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827214 | ||||||
chr3:108827268
|
G | A | 30 | a0001c0001t0001g0018a0001c0001t0001g0135a0001c0001t0001g0137others(27): Show | 34 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.8-3402G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827268 | ||||||
chr3:108827373
|
AGTATGT | A | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG01192.hp1 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.8-3294_8-3289delAT others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827373 | |||||
chr3:108827374
|
GTA | G | 6 | a0001c0001t0002g0128a0001c0001t0004g0119a0001c0001t0006g0127others(3): Show | 8 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-3294_8-3293delAT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827374 | |||||
chr3:108827375
|
T | A | 1 | a0002c0002t0002g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-3295T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827375 | ||||||
chr3:108827376
|
A | G | 1 | a0002c0002t0002g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.8-3294A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827376 | ||||||
chr3:108827377
|
T | A | 6 | a0001c0001t0002g0128a0001c0001t0004g0119a0001c0001t0006g0127others(3): Show | 8 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-3293T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827377 | ||||||
chr3:108827381
|
T | A | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG01192.hp1 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.8-3289T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827381 | ||||||
chr3:108827384
|
A | ATG | 14 | a0001c0001t0001g0206a0001c0001t0002g0161a0001c0001t0002g0191others(11): Show | 16 | HG00735.hp1 HG00741.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-3250_8-3249dupGT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | |||||
chr3:108827384
|
A | ATGTG | 3 | a0001c0001t0002g0268a0001c0001t0004g0295a0001c0001t0007g0267 | 3 | HG02280.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8-3252_8-3249dupGT others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | |||||
chr3:108827384
|
A | G | 10 | a0001c0001t0002g0128a0001c0001t0002g0260a0001c0001t0002g0261others(7): Show | 12 | HG01192.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-3286A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827384 | ||||||
chr3:108827384
|
ATG | A | 22 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(19): Show | 23 | HG01106.hp2 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-3250_8-3249delGT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | |||||
chr3:108827384
|
ATGTG | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 130 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.8-3252_8-3249delGT others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | |||||
chr3:108827384
|
ATGTGTG | A | 36 | a0001c0001t0001g0018a0001c0001t0001g0054a0001c0001t0001g0135others(33): Show | 40 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.8-3254_8-3249delGT others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | |||||
chr3:108827384
|
ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0001g0247a0001c0001t0002g0116a0001c0001t0003g0207others(1): Show | 4 | HG01952.hp2 HG02976.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3256_8-3249delGT others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | |||||
chr3:108827384
|
ATGTGTGT others(3): Show |
A | 35 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(32): Show | 42 | HG00597.hp1 HG00639.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.8-3258_8-3249delGT others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108827384 | |||||
chr3:108827413
|
T | A | 1 | a0001c0001t0001g0264 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.8-3257T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827413 | ||||||
chr3:108827482
|
C | G | 6 | a0001c0001t0002g0220a0001c0001t0007g0218a0001c0001t0007g0219others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-3188C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827482 | ||||||
chr3:108827498
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8-3172C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827498 | ||||||
chr3:108827662
|
C | T | 7 | a0001c0001t0001g0221a0001c0001t0002g0130a0001c0001t0004g0033others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-3008C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827662 | ||||||
chr3:108827823
|
T | C | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 195 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.8-2847T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827823 | ||||||
chr3:108827912
|
T | C | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG01192.hp1 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.8-2758T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827912 | ||||||
chr3:108827971
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8-2699T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108827971 | ||||||
chr3:108828100
|
A | T | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(7): Show | 10 | HG01243.hp2 HG02818.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-2570A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828100 | ||||||
chr3:108828284
|
C | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.8-2386C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828284 | ||||||
chr3:108828707
|
C | A | 5 | a0001c0001t0006g0019a0001c0001t0006g0127a0001c0001t0006g0164others(2): Show | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-1963C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828707 | ||||||
chr3:108828827
|
T | C | 4 | a0001c0001t0002g0130a0001c0001t0004g0033a0001c0001t0004g0108others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1843T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828827 | ||||||
chr3:108828871
|
TTGAAAAC others(5): Show |
T | 16 | a0001c0001t0001g0018a0001c0001t0001g0095a0001c0001t0001g0155others(13): Show | 21 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-1796_8-1785delAA others(10): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108828871 | |||||
chr3:108828995
|
C | T | 14 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0221others(11): Show | 16 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-1675C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108828995 | ||||||
chr3:108829031
|
G | T | 3 | a0001c0001t0001g0172a0001c0001t0005g0292a0001c0001t0005g0293 | 3 | HG01192.hp2 HG01516.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.8-1639G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829031 | ||||||
chr3:108829563
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.8-1107G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829563 | ||||||
chr3:108829586
|
A | AAC | 2 | a0005c0005t0002g0016a0005c0005t0002g0141 | 3 | HG02258.hp1 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.8-1054_8-1053dupCA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACAC | 10 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0045others(7): Show | 13 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.8-1056_8-1053dupCA others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACAC | 19 | a0001c0001t0001g0049a0001c0001t0001g0101a0001c0001t0001g0105others(16): Show | 20 | HG01081.hp1 HG01109.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.8-1058_8-1053dupCA others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(1): Show |
33 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0057others(30): Show | 40 | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.8-1060_8-1053dupCA others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(3): Show |
117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 134 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.8-1062_8-1053dupCA others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(5): Show |
26 | a0001c0001t0001g0012a0001c0001t0001g0085a0001c0001t0001g0086others(23): Show | 30 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.8-1064_8-1053dupCA others(10): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(7): Show |
16 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0040others(13): Show | 18 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.8-1066_8-1053dupCA others(12): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(9): Show |
34 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0092others(31): Show | 41 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.8-1068_8-1053dupCA others(14): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(11): Show |
12 | a0001c0001t0001g0043a0001c0001t0001g0179a0001c0001t0001g0180others(9): Show | 12 | HG00323.hp2 HG00741.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.8-1070_8-1053dupCA others(16): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(13): Show |
3 | a0001c0001t0002g0187a0001c0001t0002g0190a0004c0004t0008g0037 | 3 | HG02257.hp1 HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.8-1072_8-1053dupCA others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(15): Show |
1 | a0001c0001t0002g0188 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.8-1074_8-1053dupCA others(20): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | AACACACA others(19): Show |
1 | a0004c0004t0008g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8-1078_8-1053dupCA others(24): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829586 | |||||
chr3:108829586
|
A | ACACACAC others(4): Show |
2 | a0001c0001t0001g0093a0006c0006t0002g0246 | 2 | HG02273.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.8-1084_8-1083insCA others(9): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829586 | ||||||
chr3:108829586
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0002g0189 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.8-1084_8-1083insCA others(17): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829586 | ||||||
chr3:108829604
|
C | CACACAG | 4 | a0001c0001t0002g0131a0001c0001t0002g0161a0001c0001t0004g0008others(1): Show | 6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-1061_8-1060insGA others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 108829604 | |||||
chr3:108829785
|
C | T | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.8-885C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829785 | ||||||
chr3:108829961
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0116a0001c0001t0002g0117 | 4 | NA18939.hp2 NA18961.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-709G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108829961 | ||||||
chr3:108830144
|
A | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.8-526A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830144 | ||||||
chr3:108830175
|
T | G | 76 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0172others(73): Show | 86 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.8-495T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830175 | ||||||
chr3:108830202
|
T | C | 2 | a0001c0001t0003g0280a0001c0001t0003g0281 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.8-468T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830202 | ||||||
chr3:108830283
|
G | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG00408.hp1 HG00558.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-387G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830283 | ||||||
chr3:108830427
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.8-243G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 1/5 | chr3 | 108830427 | ||||||
chr3:108830815
|
C | A | 1 | a0001c0001t0002g0152 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.118+35C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830815 | ||||||
chr3:108830852
|
G | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0116a0001c0001t0002g0117 | 4 | NA18939.hp2 NA18961.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+72G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830852 | ||||||
chr3:108830873
|
T | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 143 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.118+93T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830873 | ||||||
chr3:108830927
|
G | A | 9 | a0001c0001t0001g0096a0001c0001t0001g0221a0001c0001t0002g0131others(6): Show | 11 | HG00735.hp1 HG01192.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+147G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108830927 | ||||||
chr3:108831040
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118+260A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831040 | ||||||
chr3:108831195
|
C | A | 5 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(2): Show | 5 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+415C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831195 | ||||||
chr3:108831290
|
G | C | 2 | a0006c0006t0002g0235a0006c0006t0002g0246 | 2 | NA18966.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.118+510G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831290 | ||||||
chr3:108831297
|
A | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0095a0001c0001t0001g0155others(13): Show | 21 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+517A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831297 | ||||||
chr3:108831538
|
C | CT | 16 | a0001c0001t0001g0139a0001c0001t0001g0177a0001c0001t0001g0221others(13): Show | 17 | HG01106.hp1 HG01106.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.118+777dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108831538 | |||||
chr3:108831538
|
CT | C | 41 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(38): Show | 44 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.118+777delT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108831538 | |||||
chr3:108831586
|
C | A | 4 | a0001c0001t0001g0221a0001c0001t0002g0261a0001c0001t0002g0262others(1): Show | 4 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+806C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831586 | ||||||
chr3:108831596
|
G | A | 2 | a0004c0004t0008g0037a0004c0004t0008g0038 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.118+816G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831596 | ||||||
chr3:108831703
|
C | CT | 1 | a0001c0001t0001g0004 | 3 | NA18943.hp2 NA18948.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.118+924dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108831703 | |||||
chr3:108831835
|
G | A | 4 | a0001c0001t0002g0130a0001c0001t0004g0033a0001c0001t0004g0108others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+1055G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831835 | ||||||
chr3:108831850
|
T | C | 5 | a0001c0001t0006g0019a0001c0001t0006g0127a0001c0001t0006g0164others(2): Show | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+1070T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831850 | ||||||
chr3:108831926
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.118+1146C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108831926 | ||||||
chr3:108832182
|
T | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 142 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.118+1402T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832182 | ||||||
chr3:108832334
|
G | C | 128 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0025others(125): Show | 145 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.118+1554G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832334 | ||||||
chr3:108832447
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0004g0052 | 3 | HG01069.hp2 HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.118+1667C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832447 | ||||||
chr3:108832652
|
G | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 113 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.118+1872G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832652 | ||||||
chr3:108832654
|
C | A | 6 | a0001c0001t0001g0221a0001c0001t0002g0261a0001c0001t0002g0262others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+1874C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832654 | ||||||
chr3:108832690
|
T | G | 1 | a0001c0001t0001g0026 | 2 | HG00639.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.118+1910T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832690 | ||||||
chr3:108832826
|
A | G | 3 | a0003c0003t0001g0013a0003c0003t0001g0097a0003c0003t0001g0098 | 4 | NA18948.hp1 NA18969.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+2046A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108832826 | ||||||
chr3:108833104
|
A | G | 5 | a0001c0001t0006g0019a0001c0001t0006g0127a0001c0001t0006g0164others(2): Show | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+2324A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833104 | ||||||
chr3:108833145
|
A | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA18974.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.118+2365A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833145 | ||||||
chr3:108833171
|
G | T | 1 | a0001c0001t0004g0033 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.118+2391G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833171 | ||||||
chr3:108833248
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.118+2468T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833248 | ||||||
chr3:108833286
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0004g0052 | 3 | HG01069.hp2 HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.118+2506C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833286 | ||||||
chr3:108833308
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.118+2528C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833308 | ||||||
chr3:108833310
|
C | T | 3 | a0001c0001t0007g0222a0001c0001t0007g0223a0001c0001t0007g0224 | 3 | HG01106.hp2 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.118+2530C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833310 | ||||||
chr3:108833445
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0161a0001c0001t0004g0008others(1): Show | 6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+2665G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833445 | ||||||
chr3:108833525
|
G | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 14 | HG01081.hp2 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+2745G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833525 | ||||||
chr3:108833580
|
C | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG01123.hp1 HG01433.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+2800C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833580 | ||||||
chr3:108833649
|
C | T | 2 | a0001c0001t0009g0032a0001c0001t0009g0034 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.118+2869C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833649 | ||||||
chr3:108833783
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.118+3003G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833783 | ||||||
chr3:108833799
|
T | TAC | 34 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0020others(31): Show | 40 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.118+3051_118+3052d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
T | TACAC | 22 | a0001c0001t0001g0024a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 24 | HG02080.hp1 HG02647.hp1 HG02735.hp2 others(21): Show |
intron_variant | MODIFIER | c.118+3049_118+3052d others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
T | TACACAC | 12 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(9): Show | 12 | HG01243.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.118+3047_118+3052d others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
T | TACACACA others(1): Show |
5 | a0001c0001t0002g0161a0001c0001t0004g0011a0001c0001t0004g0050others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+3045_118+3052d others(10): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
T | TACACACA others(3): Show |
12 | a0001c0001t0001g0018a0001c0001t0001g0095a0001c0001t0001g0155others(9): Show | 19 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.118+3043_118+3052d others(12): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
T | TACACACA others(9): Show |
1 | a0001c0001t0004g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.118+3037_118+3052d others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
TAC | T | 14 | a0001c0001t0002g0088a0001c0001t0002g0169a0001c0001t0004g0114others(11): Show | 15 | HG00609.hp1 HG00741.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+3051_118+3052d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
TACAC | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.118+3049_118+3052d others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833799
|
TACACAC | T | 9 | a0001c0001t0001g0081a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 10 | HG01106.hp1 HG01261.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+3047_118+3052d others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108833799 | |||||
chr3:108833879
|
G | A | 4 | a0001c0001t0002g0130a0001c0001t0004g0033a0001c0001t0004g0108others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3099G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833879 | ||||||
chr3:108833884
|
C | T | 4 | a0001c0001t0002g0130a0001c0001t0004g0033a0001c0001t0004g0108others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3104C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833884 | ||||||
chr3:108833933
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.118+3153T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108833933 | ||||||
chr3:108834113
|
C | T | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.118+3333C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834113 | ||||||
chr3:108834156
|
A | G | 1 | a0001c0001t0005g0290 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.118+3376A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834156 | ||||||
chr3:108834250
|
A | G | 2 | a0001c0001t0009g0032a0001c0001t0009g0034 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.118+3470A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834250 | ||||||
chr3:108834255
|
C | T | 1 | a0001c0001t0009g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.118+3475C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834255 | ||||||
chr3:108834273
|
C | G | 4 | a0001c0001t0002g0130a0001c0001t0004g0033a0001c0001t0004g0108others(1): Show | 4 | HG01081.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+3493C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834273 | ||||||
chr3:108834930
|
A | G | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02080.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.119-4004A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108834930 | ||||||
chr3:108835025
|
C | G | 3 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0004g0253 | 3 | HG02615.hp2 HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.119-3909C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835025 | ||||||
chr3:108835043
|
G | A | 8 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0140others(5): Show | 9 | HG01106.hp1 HG01261.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.119-3891G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835043 | ||||||
chr3:108835346
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-3588C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835346 | ||||||
chr3:108835524
|
C | T | 283 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 324 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.119-3410C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835524 | ||||||
chr3:108835584
|
T | C | 1 | a0001c0001t0011g0211 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.119-3350T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835584 | ||||||
chr3:108835629
|
C | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-3305C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835629 | ||||||
chr3:108835784
|
T | C | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-3150T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835784 | ||||||
chr3:108835895
|
GTATTTAT others(5): Show |
G | 50 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(47): Show | 56 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.119-3009_119-2998d others(14): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108835895 | |||||
chr3:108835895
|
GTATTTAT others(9): Show |
G | 233 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.119-3013_119-2998d others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108835895 | |||||
chr3:108835895
|
GTATTTAT others(13): Show |
G | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.119-3017_119-2998d others(22): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108835895 | |||||
chr3:108835983
|
G | A | 16 | a0001c0001t0001g0018a0001c0001t0001g0095a0001c0001t0001g0155others(13): Show | 21 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.119-2951G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108835983 | ||||||
chr3:108836067
|
A | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0173 | 2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.119-2867A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836067 | ||||||
chr3:108836068
|
T | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0173 | 2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.119-2866T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836068 | ||||||
chr3:108836076
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.119-2858T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836076 | ||||||
chr3:108836108
|
T | C | 3 | a0001c0001t0001g0238a0001c0001t0002g0156a0001c0001t0005g0208 | 3 | HG01952.hp1 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.119-2826T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836108 | ||||||
chr3:108836136
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.119-2798T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836136 | ||||||
chr3:108836197
|
C | G | 2 | a0001c0001t0004g0113a0001c0001t0004g0114 | 2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.119-2737C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836197 | ||||||
chr3:108836317
|
A | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-2617A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836317 | ||||||
chr3:108836368
|
T | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0045others(6): Show | 12 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.119-2566T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836368 | ||||||
chr3:108836409
|
T | C | 167 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.119-2525T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836409 | ||||||
chr3:108836415
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.119-2519A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836415 | ||||||
chr3:108836635
|
T | C | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.119-2299T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836635 | ||||||
chr3:108836639
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.119-2295T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836639 | ||||||
chr3:108836666
|
C | G | 3 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0189 | 3 | HG01496.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.119-2268C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836666 | ||||||
chr3:108836720
|
A | C | 1 | a0001c0001t0007g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.119-2214A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836720 | ||||||
chr3:108836928
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.119-2006C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836928 | ||||||
chr3:108836965
|
T | C | 52 | a0001c0001t0001g0157a0001c0001t0001g0198a0001c0001t0001g0228others(49): Show | 62 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.119-1969T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108836965 | ||||||
chr3:108837050
|
G | T | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 336 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.119-1884G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837050 | ||||||
chr3:108837174
|
T | A | 1 | a0001c0001t0002g0149 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.119-1760T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837174 | ||||||
chr3:108837398
|
C | T | 4 | a0001c0001t0004g0118a0001c0001t0004g0120a0001c0001t0004g0121others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-1536C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837398 | ||||||
chr3:108837446
|
G | C | 1 | a0001c0001t0002g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.119-1488G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837446 | ||||||
chr3:108837578
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 229 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.119-1356T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837578 | ||||||
chr3:108837673
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.119-1261T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837673 | ||||||
chr3:108837712
|
A | G | 78 | a0001c0001t0001g0157a0001c0001t0001g0198a0001c0001t0001g0228others(75): Show | 89 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.119-1222A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837712 | ||||||
chr3:108837753
|
A | T | 4 | a0001c0001t0002g0014a0001c0001t0002g0088a0001c0001t0002g0116others(1): Show | 5 | HG00609.hp1 NA18939.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-1181A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837753 | ||||||
chr3:108837780
|
T | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0229 | 3 | NA18950.hp1 NA18969.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.119-1154T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837780 | ||||||
chr3:108837809
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.119-1125T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837809 | ||||||
chr3:108837885
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.119-1049A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837885 | ||||||
chr3:108837941
|
A | G | 1 | a0001c0001t0004g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-993A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837941 | ||||||
chr3:108837985
|
G | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.119-949G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108837985 | ||||||
chr3:108838087
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.119-847T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838087 | ||||||
chr3:108838262
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.119-672C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838262 | ||||||
chr3:108838325
|
GATAGATA others(14): Show |
G | 4 | a0001c0001t0007g0222a0001c0001t0007g0223a0001c0001t0007g0224others(1): Show | 4 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-598_119-578del others(21): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838325 | |||||
chr3:108838335
|
TAGATGAT others(7): Show |
T | 13 | a0001c0001t0001g0221a0001c0001t0004g0132a0001c0001t0004g0216others(10): Show | 14 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.119-598_119-585del others(14): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838335 | ||||||
chr3:108838337
|
GATGATAG others(2): Show |
G | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(1): Show | 4 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-594_119-586del others(9): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838337 | |||||
chr3:108838344
|
GATATAGA others(8): Show |
G | 6 | a0001c0001t0002g0128a0002c0002t0002g0015a0002c0002t0002g0027others(3): Show | 8 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-588_119-574del others(15): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838344 | |||||
chr3:108838345
|
ATATAGAT others(4): Show |
A | 2 | a0002c0002t0002g0123a0002c0002t0002g0126 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.119-588_119-578del others(11): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838345 | ||||||
chr3:108838346
|
TATAGATA others(4): Show |
T | 39 | a0001c0001t0001g0138a0001c0001t0001g0228a0001c0001t0002g0117others(36): Show | 41 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.119-577_119-567del others(11): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | |||||
chr3:108838346
|
TATAGATA others(8): Show |
T | 48 | a0001c0001t0001g0198a0001c0001t0002g0001a0001c0001t0002g0014others(45): Show | 58 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.119-577_119-563del others(15): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | |||||
chr3:108838346
|
TATAGATA others(12): Show |
T | 7 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0145others(4): Show | 8 | HG00738.hp1 HG01192.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-577_119-559del others(19): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | |||||
chr3:108838346
|
TATAGATA others(20): Show |
T | 1 | a0001c0001t0002g0255 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.119-577_119-551del others(27): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838346 | |||||
chr3:108838349
|
AGATAGAT | A | 6 | a0001c0001t0002g0142a0001c0001t0002g0152a0001c0001t0002g0162others(3): Show | 6 | HG02135.hp2 HG02738.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-577_119-571del others(7): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838349 | |||||
chr3:108838356
|
T | TGATA | 30 | a0001c0001t0001g0007a0001c0001t0001g0060a0001c0001t0001g0078others(27): Show | 32 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.119-531_119-528dup others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | |||||
chr3:108838356
|
T | TGATAGAT others(1): Show |
8 | a0001c0001t0001g0047a0001c0001t0001g0080a0001c0001t0001g0091others(5): Show | 8 | HG00558.hp1 HG00621.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-535_119-528dup others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | |||||
chr3:108838356
|
TG | T | 6 | a0001c0001t0001g0042a0001c0001t0004g0216a0001c0001t0006g0164others(3): Show | 6 | HG01891.hp1 HG02717.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-577delG | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838356 | ||||||
chr3:108838356
|
TGATA | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(53): Show | 69 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.119-531_119-528del others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | |||||
chr3:108838356
|
TGATAG | T | 8 | a0001c0001t0001g0221a0001c0001t0004g0132a0001c0001t0006g0019others(5): Show | 9 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.119-577_119-573del others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838356 | ||||||
chr3:108838356
|
TGATAGAT others(1): Show |
T | 10 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0089others(7): Show | 13 | HG00408.hp2 HG00609.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.119-535_119-528del others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838356 | |||||
chr3:108838361
|
G | GAT | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0043others(1): Show | 4 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-571_119-570dup others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838361 | |||||
chr3:108838363
|
TAG | T | 4 | a0001c0001t0007g0222a0001c0001t0007g0223a0001c0001t0007g0224others(1): Show | 4 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-569_119-568del others(2): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 108838363 | |||||
chr3:108838419
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 189 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.119-515A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838419 | ||||||
chr3:108838443
|
G | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 165 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.119-491G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838443 | ||||||
chr3:108838520
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.119-414T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838520 | ||||||
chr3:108838654
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.119-280G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 2/5 | chr3 | 108838654 | ||||||
chr3:108838973
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
splice_region_variant&intron_variant | LOW | c.152+6T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108838973 | ||||||
chr3:108838980
|
T | G | 1 | a0004c0004t0008g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152+13T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108838980 | ||||||
chr3:108839197
|
T | G | 8 | a0001c0001t0002g0128a0002c0002t0002g0015a0002c0002t0002g0027others(5): Show | 10 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+230T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839197 | ||||||
chr3:108839205
|
T | C | 1 | a0001c0001t0004g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.152+238T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839205 | ||||||
chr3:108839243
|
T | C | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.152+276T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839243 | ||||||
chr3:108839382
|
C | T | 6 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0004g0132others(3): Show | 6 | HG02258.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+415C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839382 | ||||||
chr3:108839422
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.152+455A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839422 | ||||||
chr3:108839492
|
A | C | 6 | a0001c0001t0001g0236a0001c0001t0001g0249a0001c0001t0004g0008others(3): Show | 8 | HG00735.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+525A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839492 | ||||||
chr3:108839577
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.152+610C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839577 | ||||||
chr3:108839624
|
G | A | 10 | a0001c0001t0006g0019a0001c0001t0006g0127a0001c0001t0006g0164others(7): Show | 11 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+657G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839624 | ||||||
chr3:108839783
|
A | G | 100 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(97): Show | 113 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.152+816A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839783 | ||||||
chr3:108839845
|
T | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.152+878T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108839845 | ||||||
chr3:108840110
|
T | A | 5 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(2): Show | 5 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1143T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840110 | ||||||
chr3:108840110
|
T | TA | 10 | a0001c0001t0001g0244a0001c0001t0006g0019a0001c0001t0006g0127others(7): Show | 11 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+1150dupA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108840110 | |||||
chr3:108840418
|
G | T | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(11): Show | 15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.152+1451G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840418 | ||||||
chr3:108840516
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152+1549C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840516 | ||||||
chr3:108840537
|
T | TA | 165 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.152+1585dupA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108840537 | |||||
chr3:108840559
|
A | C | 12 | a0001c0001t0001g0138a0001c0001t0002g0102a0001c0001t0002g0103others(9): Show | 13 | HG01081.hp1 HG01106.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+1592A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840559 | ||||||
chr3:108840579
|
A | G | 1 | a0001c0001t0006g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+1612A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840579 | ||||||
chr3:108840710
|
G | T | 1 | a0001c0001t0007g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152+1743G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840710 | ||||||
chr3:108840777
|
A | G | 18 | a0001c0001t0002g0106a0001c0001t0002g0156a0001c0001t0002g0175others(15): Show | 19 | HG00099.hp1 HG00738.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.152+1810A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840777 | ||||||
chr3:108840816
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.152+1849G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840816 | ||||||
chr3:108840909
|
C | T | 2 | a0001c0001t0004g0011a0001c0001t0004g0052 | 3 | HG01069.hp2 HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.152+1942C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840909 | ||||||
chr3:108840936
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.152+1969C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108840936 | ||||||
chr3:108841068
|
C | T | 5 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(2): Show | 5 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+2101C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841068 | ||||||
chr3:108841071
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.152+2104T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841071 | ||||||
chr3:108841479
|
A | C | 14 | a0001c0001t0001g0018a0001c0001t0001g0095a0001c0001t0001g0101others(11): Show | 19 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+2512A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841479 | ||||||
chr3:108841495
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.152+2528A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841495 | ||||||
chr3:108841642
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+2675G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108841642 | ||||||
chr3:108842270
|
T | G | 4 | a0001c0001t0002g0128a0001c0001t0002g0131a0001c0001t0002g0158others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+3303T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842270 | ||||||
chr3:108842461
|
C | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 337 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.152+3494C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842461 | ||||||
chr3:108842487
|
A | G | 1 | a0001c0001t0002g0200 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.152+3520A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842487 | ||||||
chr3:108842562
|
C | A | 1 | a0001c0001t0004g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.152+3595C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842562 | ||||||
chr3:108842630
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 226 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.152+3663T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842630 | ||||||
chr3:108842642
|
C | T | 1 | a0001c0001t0013g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.152+3675C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842642 | ||||||
chr3:108842848
|
A | G | 8 | a0001c0001t0001g0096a0002c0002t0002g0015a0002c0002t0002g0027others(5): Show | 10 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+3881A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108842848 | ||||||
chr3:108843102
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.153-3966G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843102 | ||||||
chr3:108843121
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0003g0274 | 2 | HG00544.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.153-3947T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843121 | ||||||
chr3:108843173
|
C | G | 1 | a0001c0001t0007g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.153-3895C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843173 | ||||||
chr3:108843214
|
T | C | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153-3854T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843214 | ||||||
chr3:108843269
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG02080.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.153-3799C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843269 | ||||||
chr3:108843316
|
G | A | 6 | a0001c0001t0001g0221a0001c0001t0004g0108a0004c0004t0008g0037others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-3752G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843316 | ||||||
chr3:108843330
|
G | A | 11 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(8): Show | 12 | HG01081.hp1 HG01106.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-3738G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843330 | ||||||
chr3:108843462
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.153-3606G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843462 | ||||||
chr3:108843467
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153-3601T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843467 | ||||||
chr3:108843545
|
A | G | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-3523A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843545 | ||||||
chr3:108843607
|
C | A | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-3461C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843607 | ||||||
chr3:108843609
|
C | T | 7 | a0001c0001t0001g0079a0001c0001t0001g0194a0001c0001t0001g0206others(4): Show | 7 | HG00642.hp1 HG01255.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-3459C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843609 | ||||||
chr3:108843799
|
C | T | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0167 | 3 | HG03098.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.153-3269C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108843799 | ||||||
chr3:108844002
|
T | G | 291 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(288): Show | 335 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.153-3066T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844002 | ||||||
chr3:108844083
|
G | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.153-2985G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844083 | ||||||
chr3:108844224
|
A | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.153-2844A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844224 | ||||||
chr3:108844299
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.153-2769G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844299 | ||||||
chr3:108844319
|
A | AT | 22 | a0001c0001t0001g0071a0001c0001t0001g0087a0001c0001t0001g0244others(19): Show | 26 | HG00735.hp1 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.153-2733dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844319 | |||||
chr3:108844398
|
T | G | 6 | a0001c0001t0002g0128a0001c0001t0002g0131a0001c0001t0002g0158others(3): Show | 6 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-2670T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844398 | ||||||
chr3:108844456
|
T | A | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2612T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844456 | ||||||
chr3:108844457
|
G | A | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2611G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844457 | ||||||
chr3:108844458
|
G | T | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2610G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844458 | ||||||
chr3:108844460
|
C | A | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2608C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844460 | ||||||
chr3:108844463
|
T | A | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2605T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844463 | ||||||
chr3:108844464
|
G | A | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2604G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844464 | ||||||
chr3:108844466
|
T | TTAATTTA others(27): Show |
7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2602_153-2601i others(36): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844466 | ||||||
chr3:108844468
|
A | T | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2600A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844468 | ||||||
chr3:108844490
|
T | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG01243.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-2578T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844490 | ||||||
chr3:108844499
|
G | T | 5 | a0001c0001t0004g0118a0001c0001t0004g0120a0001c0001t0004g0121others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-2569G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844499 | ||||||
chr3:108844502
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0130a0001c0001t0005g0291 | 3 | HG02572.hp2 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.153-2566C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844502 | ||||||
chr3:108844507
|
A | G | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-2561A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844507 | ||||||
chr3:108844608
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-2460G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844608 | ||||||
chr3:108844691
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-2377A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844691 | ||||||
chr3:108844781
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.153-2287T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844781 | ||||||
chr3:108844842
|
T | C | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.153-2226T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844842 | ||||||
chr3:108844843
|
C | CA | 55 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0022others(52): Show | 63 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.153-2199dupA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844843
|
C | CAA | 25 | a0001c0001t0001g0221a0001c0001t0002g0021a0001c0001t0002g0088others(22): Show | 26 | HG00609.hp1 HG01106.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.153-2200_153-2199d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844843
|
C | CAAA | 12 | a0001c0001t0002g0014a0001c0001t0004g0008a0001c0001t0004g0112others(9): Show | 17 | HG00735.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-2201_153-2199d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844843
|
C | CAAAA | 8 | a0001c0001t0002g0117a0001c0001t0004g0108a0001c0001t0013g0122others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-2202_153-2199d others(6): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844843
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-2211_153-2199d others(15): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844843
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0006g0019a0001c0001t0006g0165 | 3 | HG02886.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.153-2214_153-2199d others(18): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844843
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0006g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.153-2215_153-2199d others(19): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844843
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0006g0164 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.153-2219_153-2199d others(23): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844843 | |||||
chr3:108844859
|
A | G | 1 | a0001c0001t0004g0295 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.153-2209A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844859 | ||||||
chr3:108844861
|
A | AG | 7 | a0001c0001t0001g0046a0001c0001t0001g0067a0001c0001t0001g0085others(4): Show | 7 | HG02630.hp2 HG02738.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-2207_153-2206i others(3): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844861 | ||||||
chr3:108844861
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 173 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.153-2207A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844861 | ||||||
chr3:108844865
|
AAAAAG | A | 6 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0136others(3): Show | 7 | HG01081.hp1 HG01106.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-2199_153-2195d others(7): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 108844865 | |||||
chr3:108844870
|
G | A | 5 | a0001c0001t0006g0019a0001c0001t0006g0127a0001c0001t0006g0164others(2): Show | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-2198G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844870 | ||||||
chr3:108844874
|
T | A | 1 | a0001c0001t0006g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.153-2194T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844874 | ||||||
chr3:108844969
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.153-2099T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108844969 | ||||||
chr3:108845042
|
A | G | 2 | a0001c0001t0009g0032a0001c0001t0009g0034 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.153-2026A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845042 | ||||||
chr3:108845133
|
G | C | 131 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0017others(128): Show | 146 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.153-1935G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845133 | ||||||
chr3:108845141
|
C | T | 2 | a0001c0001t0009g0032a0001c0001t0009g0034 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.153-1927C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845141 | ||||||
chr3:108845144
|
A | T | 2 | a0001c0001t0009g0032a0001c0001t0009g0034 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.153-1924A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845144 | ||||||
chr3:108845251
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.153-1817G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845251 | ||||||
chr3:108845503
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0109 | 2 | HG00408.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.153-1565C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845503 | ||||||
chr3:108845710
|
T | A | 1 | a0001c0001t0003g0294 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153-1358T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845710 | ||||||
chr3:108845714
|
T | C | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-1354T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845714 | ||||||
chr3:108845774
|
G | A | 6 | a0001c0001t0004g0113a0001c0001t0004g0114a0001c0001t0004g0132others(3): Show | 6 | HG02258.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-1294G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845774 | ||||||
chr3:108845883
|
G | A | 93 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0017others(90): Show | 104 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.153-1185G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845883 | ||||||
chr3:108845893
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.153-1175C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845893 | ||||||
chr3:108845937
|
A | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0095a0001c0001t0001g0101others(12): Show | 21 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.153-1131A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845937 | ||||||
chr3:108845962
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.153-1106C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108845962 | ||||||
chr3:108846211
|
T | C | 1 | a0001c0001t0003g0270 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.153-857T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846211 | ||||||
chr3:108846549
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.153-519G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846549 | ||||||
chr3:108846560
|
T | C | 274 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.153-508T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846560 | ||||||
chr3:108846657
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.153-411A>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846657 | ||||||
chr3:108846708
|
T | C | 1 | a0001c0001t0002g0116 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.153-360T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846708 | ||||||
chr3:108846783
|
G | T | 101 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0017others(98): Show | 114 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.153-285G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846783 | ||||||
chr3:108846791
|
G | A | 269 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.153-277G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846791 | ||||||
chr3:108846866
|
T | C | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-202T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846866 | ||||||
chr3:108846968
|
T | C | 274 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(271): Show | 315 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.153-100T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108846968 | ||||||
chr3:108847031
|
G | A | 1 | a0001c0001t0003g0277 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.153-37G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 3/5 | chr3 | 108847031 | ||||||
chr3:108847216
|
A | G | 5 | a0001c0001t0004g0118a0001c0001t0004g0120a0001c0001t0004g0121others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+87A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847216 | ||||||
chr3:108847244
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214+115A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847244 | ||||||
chr3:108847370
|
T | C | 3 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0167 | 3 | HG03098.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214+241T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847370 | ||||||
chr3:108847551
|
C | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 217 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.214+422C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847551 | ||||||
chr3:108847591
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0001t0001g0170 | 3 | HG00438.hp2 HG00544.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.214+462G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847591 | ||||||
chr3:108847651
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.214+522G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847651 | ||||||
chr3:108847956
|
G | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 216 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.214+827G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108847956 | ||||||
chr3:108848026
|
A | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0190 | 2 | HG01257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.214+897A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848026 | ||||||
chr3:108848131
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.214+1002T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848131 | ||||||
chr3:108848165
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.215-1001A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848165 | ||||||
chr3:108848188
|
G | A | 1 | a0001c0001t0003g0294 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.215-978G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848188 | ||||||
chr3:108848302
|
T | C | 1 | a0001c0001t0013g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.215-864T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848302 | ||||||
chr3:108848368
|
T | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.215-798T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848368 | ||||||
chr3:108848443
|
T | A | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.215-723T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848443 | ||||||
chr3:108848517
|
G | T | 5 | a0001c0001t0004g0118a0001c0001t0004g0120a0001c0001t0004g0121others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-649G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848517 | ||||||
chr3:108848602
|
G | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.215-564G>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848602 | ||||||
chr3:108848678
|
C | A | 2 | a0001c0001t0003g0271a0001c0001t0003g0272 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.215-488C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848678 | ||||||
chr3:108848683
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.215-483T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848683 | ||||||
chr3:108848820
|
A | G | 5 | a0001c0001t0004g0118a0001c0001t0004g0120a0001c0001t0004g0121others(2): Show | 5 | HG01891.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-346A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848820 | ||||||
chr3:108848833
|
G | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0017others(78): Show | 91 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.215-333G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848833 | ||||||
chr3:108848859
|
A | G | 1 | a0001c0001t0003g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.215-307A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108848859 | ||||||
chr3:108849002
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-164C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108849002 | ||||||
chr3:108849076
|
G | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.215-90G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 4/5 | chr3 | 108849076 | ||||||
chr3:108849352
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.303+98A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849352 | ||||||
chr3:108849416
|
C | G | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.303+162C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849416 | ||||||
chr3:108849477
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+223A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849477 | ||||||
chr3:108849479
|
G | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+225G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849479 | ||||||
chr3:108849569
|
C | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.303+315C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849569 | ||||||
chr3:108849778
|
C | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+524C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849778 | ||||||
chr3:108849857
|
T | G | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.303+603T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849857 | ||||||
chr3:108849903
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+649G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108849903 | ||||||
chr3:108850029
|
T | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+775T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850029 | ||||||
chr3:108850063
|
T | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 234 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.303+809T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850063 | ||||||
chr3:108850123
|
T | A | 2 | a0005c0005t0002g0016a0005c0005t0002g0141 | 3 | HG02258.hp1 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.303+869T>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850123 | ||||||
chr3:108850186
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.303+932T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850186 | ||||||
chr3:108850200
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+946A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850200 | ||||||
chr3:108850273
|
T | C | 2 | a0001c0001t0002g0163a0001c0001t0002g0169 | 2 | HG00741.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.303+1019T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850273 | ||||||
chr3:108850306
|
C | CT | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 200 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.303+1066dupT | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108850306 | |||||
chr3:108850306
|
C | CTTT | 16 | a0001c0001t0001g0009a0001c0001t0001g0095a0001c0001t0001g0101others(13): Show | 22 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.303+1064_303+1066d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108850306 | |||||
chr3:108850333
|
T | G | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+1079T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850333 | ||||||
chr3:108850337
|
C | A | 2 | a0001c0001t0004g0050a0001c0001t0004g0119 | 2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.303+1083C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850337 | ||||||
chr3:108850357
|
T | G | 1 | a0001c0001t0004g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+1103T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850357 | ||||||
chr3:108850387
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+1133C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850387 | ||||||
chr3:108850398
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+1144G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850398 | ||||||
chr3:108850486
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.303+1232G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850486 | ||||||
chr3:108850505
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+1251A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850505 | ||||||
chr3:108850520
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+1266G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850520 | ||||||
chr3:108850579
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.303+1325C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850579 | ||||||
chr3:108850696
|
T | C | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+1442T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850696 | ||||||
chr3:108850703
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.303+1449T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850703 | ||||||
chr3:108850733
|
T | C | 20 | a0001c0001t0004g0008a0001c0001t0004g0011a0001c0001t0004g0033others(17): Show | 23 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.303+1479T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850733 | ||||||
chr3:108850859
|
T | G | 1 | a0001c0001t0001g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.303+1605T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850859 | ||||||
chr3:108850917
|
T | G | 1 | a0001c0001t0013g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303+1663T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108850917 | ||||||
chr3:108851059
|
T | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 226 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.303+1805T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851059 | ||||||
chr3:108851225
|
G | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.303+1971G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851225 | ||||||
chr3:108851407
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.303+2153C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851407 | ||||||
chr3:108851453
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0095a0001c0001t0001g0101others(13): Show | 22 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.304-2167A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851453 | ||||||
chr3:108851491
|
T | C | 3 | a0001c0001t0004g0112a0001c0001t0009g0032a0001c0001t0009g0034 | 3 | HG01884.hp2 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.304-2129T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851491 | ||||||
chr3:108851549
|
G | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.304-2071G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851549 | ||||||
chr3:108851582
|
G | T | 1 | a0001c0001t0003g0282 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.304-2038G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851582 | ||||||
chr3:108851628
|
TA | T | 7 | a0001c0001t0001g0069a0001c0001t0001g0258a0001c0001t0002g0160others(4): Show | 7 | HG02080.hp2 HG02647.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-1978delA | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851628 | |||||
chr3:108851628
|
TAA | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 213 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.304-1979_304-1978d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851628 | |||||
chr3:108851628
|
TAAA | T | 7 | a0001c0001t0001g0221a0001c0001t0004g0008a0001c0001t0004g0033others(4): Show | 9 | HG00735.hp1 HG01081.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1980_304-1978d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851628 | |||||
chr3:108851715
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.304-1905C>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851715 | ||||||
chr3:108851764
|
T | G | 1 | a0001c0001t0004g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.304-1856T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851764 | ||||||
chr3:108851821
|
G | A | 4 | a0004c0004t0008g0037a0004c0004t0008g0038a0004c0004t0008g0051others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-1799G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108851821 | ||||||
chr3:108851870
|
AGTTGACC others(4): Show |
A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 225 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.304-1741_304-1731d others(13): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108851870 | |||||
chr3:108852014
|
C | G | 7 | a0001c0001t0004g0008a0001c0001t0004g0033a0001c0001t0004g0050others(4): Show | 9 | HG00735.hp1 HG01081.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1606C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852014 | ||||||
chr3:108852062
|
C | CACA | 8 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 8 | HG01081.hp1 HG01123.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.304-1532_304-1530d others(5): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852062 | |||||
chr3:108852062
|
CACAACA | C | 7 | a0002c0002t0002g0015a0002c0002t0002g0027a0002c0002t0002g0123others(4): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1535_304-1530d others(8): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852062 | |||||
chr3:108852202
|
G | A | 20 | a0001c0001t0004g0008a0001c0001t0004g0011a0001c0001t0004g0033others(17): Show | 23 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.304-1418G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852202 | ||||||
chr3:108852209
|
C | T | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 180 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.304-1411C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852209 | ||||||
chr3:108852352
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304-1268G>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852352 | ||||||
chr3:108852369
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.304-1251G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852369 | ||||||
chr3:108852397
|
G | GCA | 1 | a0001c0001t0004g0008 | 3 | HG00735.hp1 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.304-1198_304-1197d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852397 | |||||
chr3:108852397
|
GCA | G | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(280): Show | 323 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.304-1198_304-1197d others(4): Show |
TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 108852397 | |||||
chr3:108852495
|
A | G | 9 | a0001c0001t0004g0112a0001c0001t0007g0218a0001c0001t0007g0219others(6): Show | 9 | HG01106.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.304-1125A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852495 | ||||||
chr3:108852575
|
A | G | 3 | a0001c0001t0002g0128a0001c0001t0005g0266a0001c0001t0005g0285 | 3 | HG02895.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.304-1045A>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852575 | ||||||
chr3:108852629
|
T | G | 6 | a0001c0001t0007g0218a0001c0001t0007g0219a0001c0001t0007g0222others(3): Show | 6 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-991T>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852629 | ||||||
chr3:108852692
|
T | C | 5 | a0001c0001t0006g0019a0001c0001t0006g0127a0001c0001t0006g0164others(2): Show | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-928T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852692 | ||||||
chr3:108852740
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0252 | 2 | NA18993.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.304-880C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852740 | ||||||
chr3:108852987
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.304-633G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852987 | ||||||
chr3:108852997
|
G | A | 1 | a0001c0001t0003g0030 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.304-623G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108852997 | ||||||
chr3:108853132
|
T | C | 10 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0136others(7): Show | 11 | HG01081.hp1 HG01106.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-488T>C | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853132 | ||||||
chr3:108853134
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304-486C>G | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853134 | ||||||
chr3:108853277
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.304-343G>A | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853277 | ||||||
chr3:108853393
|
A | T | 5 | a0001c0001t0004g0008a0001c0001t0004g0033a0001c0001t0004g0050others(2): Show | 7 | HG00735.hp1 HG01081.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-227A>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853393 | ||||||
chr3:108853544
|
C | T | 5 | a0001c0001t0006g0019a0001c0001t0006g0127a0001c0001t0006g0164others(2): Show | 6 | HG02717.hp1 HG02886.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-76C>T | TRAT1 | ENSG00000163519.14 | transcript | ENST00000295756.11 | protein_coding | 5/5 | chr3 | 108853544 |