geneid | 96764 |
---|---|
ensemblid | ENSG00000137574.11 |
hgncid | 17843 |
symbol | TGS1 |
name | trimethylguanosine synthase 1 |
refseq_nuc | NM_024831.8 |
refseq_prot | NP_079107.6 |
ensembl_nuc | ENST00000260129.6 |
ensembl_prot | ENSP00000260129.5 |
mane_status | MANE Select |
chr | chr8 |
start | 55773446 |
end | 55826445 |
strand | + |
ver | v1.2 |
region | chr8:55773446-55826445 |
region5000 | chr8:55768446-55831445 |
regionname0 | TGS1_chr8_55773446_55826445 |
regionname5000 | TGS1_chr8_55768446_55831445 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 853 | 303 | 57 | 48 | 152 | 11 | 34 | 112 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0002 | 0/0 | 853 | 27 | 13 | 7 | 1 | 1 | 5 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0003 | 0/0 | 853 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0004 | 0/0 | 853 | 6 | 2 | 1 | 2 | 0 | 1 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0005 | 0/0 | 853 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0006 | 0/0 | 853 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0007 | 0/0 | 853 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0008 | 0/0 | 853 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0009 | 0/0 | 853 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0010 | 1/0 | 853 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0011 | 0/0 | 853 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0012 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0013 | 0/0 | 853 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0014 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0015 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0016 | 0/0 | 853 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0017 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0018 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0019 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0020 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2562 | 292 | 56 | 45 | 151 | 11 | 28 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0002 | 0/0 | 2562 | 25 | 13 | 5 | 1 | 1 | 5 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0003 | 0/0 | 2562 | 8 | 7 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0004 | 0/0 | 2562 | 6 | 2 | 1 | 2 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0005 | 0/0 | 2562 | 5 | 5 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0006 | 0/0 | 2562 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0007 | 0/0 | 2562 | 3 | 0 | 0 | 0 | 0 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0008 | 0/0 | 2562 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0009 | 0/0 | 2562 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0010 | 0/0 | 2562 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0011 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0012 | 0/0 | 2562 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0013 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0014 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0015 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0016 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0017 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0018 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0019 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0020 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0021 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0022 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0023 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0024 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0025 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0026 | 1/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0027 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0028 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
c0029 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1916 | 215 | 49 | 36 | 98 | 7 | 25 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0002 | 0/1 | 1916 | 69 | 3 | 9 | 47 | 2 | 7 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0003 | 0/0 | 1917 | 33 | 17 | 6 | 1 | 1 | 8 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0004 | 0/0 | 1914 | 13 | 2 | 6 | 0 | 2 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0005 | 0/0 | 1916 | 8 | 7 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0006 | 0/0 | 1916 | 7 | 0 | 0 | 7 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0007 | 0/0 | 1911 | 5 | 5 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0008 | 0/0 | 1916 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0009 | 0/0 | 1917 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0010 | 0/0 | 1916 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0011 | 0/0 | 1917 | 2 | 1 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0012 | 1/0 | 1916 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0013 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0014 | 0/0 | 1916 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0015 | 0/0 | 1916 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0016 | 0/0 | 1916 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0017 | 0/0 | 1916 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
t0018 | 0/0 | 1916 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0002 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0003 | 0/1 | 4 | 0 | 1 | 1 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2562 | 292 | 56 | 45 | 151 | 11 | 28 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0007 | 0/0 | 2562 | 3 | 0 | 0 | 0 | 0 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0008 | 0/0 | 2562 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0009 | 0/0 | 2562 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0014 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0016 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0017 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0020 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0002c0002 | 0/0 | 2562 | 25 | 13 | 5 | 1 | 1 | 5 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0002c0027 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0002c0029 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0003c0003 | 0/0 | 2562 | 8 | 7 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0004c0004 | 0/0 | 2562 | 6 | 2 | 1 | 2 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0005c0005 | 0/0 | 2562 | 5 | 5 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0006c0006 | 0/0 | 2562 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0007c0012 | 0/0 | 2562 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0008c0011 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0009c0010 | 0/0 | 2562 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0010c0026 | 1/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0011c0028 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0012c0025 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0013c0013 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0014c0015 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0015c0022 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0016c0021 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0017c0019 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0018c0018 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0019c0023 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0020c0024 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4477 | 190 | 42 | 29 | 95 | 7 | 17 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0002 | 0/1 | 4477 | 65 | 1 | 9 | 45 | 2 | 7 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0004 | 0/0 | 4475 | 13 | 2 | 6 | 0 | 2 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0006 | 0/0 | 4477 | 6 | 0 | 0 | 6 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0007 | 0/0 | 4472 | 5 | 5 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0008 | 0/0 | 4477 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0010 | 0/0 | 4477 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0011 | 0/0 | 4478 | 2 | 1 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0014 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0015 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0017 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0001t0018 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0007t0001 | 0/0 | 4477 | 3 | 0 | 0 | 0 | 0 | 3 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0008t0001 | 0/0 | 4477 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0009t0001 | 0/0 | 4477 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0014t0001 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0016t0006 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0017t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0001c0020t0001 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0002c0002t0003 | 0/0 | 4478 | 25 | 13 | 5 | 1 | 1 | 5 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0002c0027t0003 | 0/0 | 4478 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0002c0029t0013 | 0/0 | 4478 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0003c0003t0005 | 0/0 | 4477 | 8 | 7 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0004c0004t0001 | 0/0 | 4477 | 6 | 2 | 1 | 2 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0005c0005t0002 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0005c0005t0009 | 0/0 | 4478 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0006c0006t0003 | 0/0 | 4478 | 4 | 4 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0007c0012t0003 | 0/0 | 4478 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0008c0011t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0008c0011t0016 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0009c0010t0001 | 0/0 | 4477 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0010c0026t0012 | 1/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0011c0028t0003 | 0/0 | 4478 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0012c0025t0002 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0013c0013t0001 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0014c0015t0002 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0015c0022t0002 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0016c0021t0001 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0017c0019t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0018c0018t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0019c0023t0001 | 0/0 | 4477 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
a0020c0024t0001 | 0/0 | 4477 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | copy fasta | chr8 | 55768446 | 55831445 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0003 | 0/1 | 4 | 0 | 1 | 1 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0002 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0011g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0015g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0017g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0001t0018g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0007t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0007t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0008t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0008t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0009t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0014t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0016t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0017t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0001c0020t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0002t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0027t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0002c0029t0013g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0003c0003t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0004c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0005c0005t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0006c0006t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0006c0006t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0007c0012t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0007c0012t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0008c0011t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0008c0011t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0009c0010t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0010c0026t0012g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0011c0028t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0012c0025t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0013c0013t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0014c0015t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0015c0022t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0016c0021t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0017c0019t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0018c0018t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0019c0023t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
a0020c0024t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0003 | g0288 | EUR | GBR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00597 | hp1 | a0012 | c0025 | t0002 | g0089 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00639 | hp2 | a0002 | c0027 | t0003 | g0302 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00642 | hp1 | a0001 | c0001 | t0015 | g0178 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00738 | hp1 | a0001 | c0008 | t0001 | g0186 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00741 | hp1 | a0002 | c0002 | t0003 | g0294 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01070 | hp2 | a0009 | c0010 | t0001 | g0030 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01071 | hp2 | a0009 | c0010 | t0001 | g0030 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01109 | hp1 | a0003 | c0003 | t0005 | g0312 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01175 | hp1 | a0001 | c0014 | t0001 | g0154 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01192 | hp1 | a0004 | c0004 | t0001 | g0320 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01255 | hp2 | a0002 | c0002 | t0003 | g0324 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0300 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01258 | hp1 | a0002 | c0002 | t0003 | g0301 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01433 | hp2 | a0001 | c0008 | t0001 | g0175 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0005 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01884 | hp1 | a0005 | c0005 | t0009 | g0310 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0202 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0306 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01975 | hp2 | a0013 | c0013 | t0001 | g0180 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02055 | hp1 | a0001 | c0001 | t0014 | g0210 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02055 | hp2 | a0002 | c0002 | t0003 | g0290 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02129 | hp2 | a0001 | c0001 | t0018 | g0251 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02145 | hp1 | a0006 | c0006 | t0003 | g0296 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0303 | EAS | CDX | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02257 | hp1 | a0001 | c0017 | t0001 | g0230 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02257 | hp2 | a0003 | c0003 | t0005 | g0318 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02258 | hp2 | a0014 | c0015 | t0002 | g0311 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02451 | hp1 | a0006 | c0006 | t0003 | g0010 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02523 | hp2 | a0001 | c0016 | t0006 | g0032 | EAS | KHV | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0291 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02615 | hp2 | a0019 | c0023 | t0001 | g0322 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02622 | hp1 | a0002 | c0002 | t0003 | g0285 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02622 | hp2 | a0004 | c0004 | t0001 | g0323 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02698 | hp1 | a0001 | c0009 | t0001 | g0014 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0034 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02723 | hp2 | a0003 | c0003 | t0005 | g0316 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0297 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0054 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02738 | hp2 | a0011 | c0028 | t0003 | g0308 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02809 | hp1 | a0006 | c0006 | t0003 | g0010 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02809 | hp2 | a0018 | c0018 | t0001 | g0325 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02818 | hp1 | a0003 | c0003 | t0005 | g0313 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02896 | hp2 | a0002 | c0002 | t0003 | g0293 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0298 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02922 | hp2 | a0008 | c0011 | t0001 | g0112 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02965 | hp1 | a0005 | c0005 | t0002 | g0309 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0287 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0205 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02976 | hp1 | a0017 | c0019 | t0001 | g0121 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0281 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0286 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03098 | hp1 | a0003 | c0003 | t0005 | g0315 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0292 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03139 | hp1 | a0005 | c0005 | t0009 | g0278 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03225 | hp2 | a0004 | c0004 | t0001 | g0321 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03486 | hp2 | a0003 | c0003 | t0005 | g0319 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03516 | hp2 | a0008 | c0011 | t0016 | g0143 | AFR | ESN | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0207 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03579 | hp2 | a0006 | c0006 | t0003 | g0010 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03669 | hp1 | a0001 | c0009 | t0001 | g0014 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03669 | hp2 | a0004 | c0004 | t0001 | g0264 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0305 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03704 | hp1 | a0001 | c0020 | t0001 | g0183 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03704 | hp2 | a0016 | c0021 | t0001 | g0255 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03942 | hp1 | a0002 | c0002 | t0003 | g0299 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03942 | hp2 | a0001 | c0007 | t0001 | g0258 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04115 | hp2 | a0001 | c0007 | t0001 | g0270 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04184 | hp1 | a0007 | c0012 | t0003 | g0284 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0307 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0047 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG04228 | hp2 | a0002 | c0002 | t0003 | g0304 | SAS | STU | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0206 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18906 | hp1 | a0003 | c0003 | t0005 | g0314 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18939 | hp2 | a0001 | c0001 | t0010 | g0209 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18950 | hp1 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18960 | hp2 | a0004 | c0004 | t0001 | g0185 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18965 | hp1 | a0001 | c0001 | t0010 | g0268 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18972 | hp2 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19030 | hp1 | a0005 | c0005 | t0009 | g0280 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19059 | hp1 | a0015 | c0022 | t0002 | g0051 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19059 | hp2 | a0004 | c0004 | t0001 | g0035 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19076 | hp1 | a0020 | c0024 | t0001 | g0139 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19085 | hp2 | a0001 | c0001 | t0010 | g0236 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ASW | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ASW | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20905 | hp1 | a0007 | c0012 | t0003 | g0289 | SAS | GIH | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20905 | hp2 | a0001 | c0007 | t0001 | g0257 | SAS | GIH | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG01123 | hp2 | a0002 | c0029 | t0013 | g0283 | AMR | CLM | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02109 | hp1 | a0005 | c0005 | t0009 | g0279 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | ACB | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03471 | hp1 | a0003 | c0003 | t0005 | g0317 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0295 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0003 | REF | REF | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
homoSapiens_grch38 | hp1 | a0010 | c0026 | t0012 | g0282 | REF | REF | TGS1_chr8_55768446_55831445 | TGS1 | chr8 | 55768446 | 55831445 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55773665
|
T | C | 13 | a0001a0004a0008others(10): Show | 322 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
missense_variant | MODERATE | c.47T>C | p.Ile16Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/13 | 220/4477 | 47/2562 | 16/853 | chr8 | 55773665 | ||
chr8:55782786
|
A | G | 1 | a0012 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.140A>G | p.Tyr47Cys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/13 | 313/4477 | 140/2562 | 47/853 | chr8 | 55782786 | ||
chr8:55785728
|
C | T | 1 | a0020 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.176C>T | p.Ala59Val | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 3/13 | 349/4477 | 176/2562 | 59/853 | chr8 | 55785728 | ||
chr8:55785806
|
G | A | 1 | a0013 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.254G>A | p.Ser85Asn | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 3/13 | 427/4477 | 254/2562 | 85/853 | chr8 | 55785806 | ||
chr8:55786265
|
A | G | 1 | a0008 | 2 | HG02922.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.367A>G | p.Lys123Glu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 540/4477 | 367/2562 | 123/853 | chr8 | 55786265 | ||
chr8:55786356
|
C | T | 1 | a0011 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.458C>T | p.Ala153Val | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 631/4477 | 458/2562 | 153/853 | chr8 | 55786356 | ||
chr8:55786376
|
A | G | 3 | a0004a0009a0019 | 9 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(6): Show |
missense_variant | MODERATE | c.478A>G | p.Ile160Val | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 651/4477 | 478/2562 | 160/853 | chr8 | 55786376 | ||
chr8:55786599
|
A | G | 1 | a0007 | 2 | HG04184.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.701A>G | p.Lys234Arg | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 874/4477 | 701/2562 | 234/853 | chr8 | 55786599 | ||
chr8:55786698
|
G | C | 1 | a0019 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.800G>C | p.Ser267Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 973/4477 | 800/2562 | 267/853 | chr8 | 55786698 | ||
chr8:55786793
|
C | T | 1 | a0003 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.895C>T | p.Pro299Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1068/4477 | 895/2562 | 299/853 | chr8 | 55786793 | ||
chr8:55787001
|
G | C | 1 | a0014 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1103G>C | p.Gly368Ala | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1276/4477 | 1103/2562 | 368/853 | chr8 | 55787001 | ||
chr8:55787028
|
C | T | 1 | a0009 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.1130C>T | p.Ser377Leu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1303/4477 | 1130/2562 | 377/853 | chr8 | 55787028 | ||
chr8:55790199
|
G | A | 1 | a0018 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1180G>A | p.Gly394Arg | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/13 | 1353/4477 | 1180/2562 | 394/853 | chr8 | 55790199 | ||
chr8:55790239
|
C | G | 1 | a0018 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1220C>G | p.Thr407Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/13 | 1393/4477 | 1220/2562 | 407/853 | chr8 | 55790239 | ||
chr8:55792721
|
A | C | 1 | a0018 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1304A>C | p.Asn435Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/13 | 1477/4477 | 1304/2562 | 435/853 | chr8 | 55792721 | ||
chr8:55796142
|
T | C | 7 | a0002a0003a0005others(4): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
missense_variant | MODERATE | c.1532T>C | p.Ile511Thr | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/13 | 1705/4477 | 1532/2562 | 511/853 | chr8 | 55796142 | ||
chr8:55799097
|
G | A | 1 | a0003 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.1726G>A | p.Val576Ile | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/13 | 1899/4477 | 1726/2562 | 576/853 | chr8 | 55799097 | ||
chr8:55799112
|
G | A | 1 | a0017 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1741G>A | p.Glu581Lys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/13 | 1914/4477 | 1741/2562 | 581/853 | chr8 | 55799112 | ||
chr8:55799154
|
A | G | 4 | a0002a0006a0007others(1): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
missense_variant | MODERATE | c.1783A>G | p.Thr595Ala | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/13 | 1956/4477 | 1783/2562 | 595/853 | chr8 | 55799154 | ||
chr8:55802576
|
C | T | 1 | a0015 | 1 | NA19059.hp1 | missense_variant | MODERATE | c.1969C>T | p.Arg657Cys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/13 | 2142/4477 | 1969/2562 | 657/853 | chr8 | 55802576 | ||
chr8:55804956
|
C | T | 1 | a0016 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.2063C>T | p.Ser688Phe | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/13 | 2236/4477 | 2063/2562 | 688/853 | chr8 | 55804956 | ||
chr8:55810998
|
T | G | 7 | a0002a0003a0005others(4): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
missense_variant | MODERATE | c.2261T>G | p.Phe754Cys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/13 | 2434/4477 | 2261/2562 | 754/853 | chr8 | 55810998 | ||
chr8:55813044
|
G | A | 1 | a0006 | 4 | HG02145.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.2365G>A | p.Glu789Lys | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/13 | 2538/4477 | 2365/2562 | 789/853 | chr8 | 55813044 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55786345
|
C | T | 1 | a0002c0029 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.447C>T | p.Asp149Asp | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 620/4477 | 447/2562 | 149/853 | chr8 | 55786345 | ||
chr8:55786555
|
G | A | 1 | a0001c0014 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.657G>A | p.Pro219Pro | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 830/4477 | 657/2562 | 219/853 | chr8 | 55786555 | ||
chr8:55786564
|
A | C | 1 | a0001c0009 | 2 | HG02698.hp1 HG03669.hp1 |
synonymous_variant | LOW | c.666A>C | p.Ala222Ala | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 839/4477 | 666/2562 | 222/853 | chr8 | 55786564 | ||
chr8:55786978
|
C | T | 1 | a0002c0027 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1080C>T | p.Ser360Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1253/4477 | 1080/2562 | 360/853 | chr8 | 55786978 | ||
chr8:55786990
|
A | G | 1 | a0001c0007 | 3 | HG03942.hp2 HG04115.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.1092A>G | p.Glu364Glu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1265/4477 | 1092/2562 | 364/853 | chr8 | 55786990 | ||
chr8:55787014
|
G | A | 1 | a0001c0016 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1116G>A | p.Glu372Glu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1289/4477 | 1116/2562 | 372/853 | chr8 | 55787014 | ||
chr8:55787029
|
G | A | 1 | a0001c0017 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1131G>A | p.Ser377Ser | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/13 | 1304/4477 | 1131/2562 | 377/853 | chr8 | 55787029 | ||
chr8:55796011
|
G | A | 1 | a0003c0003 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
synonymous_variant | LOW | c.1401G>A | p.Gln467Gln | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/13 | 1574/4477 | 1401/2562 | 467/853 | chr8 | 55796011 | ||
chr8:55796023
|
A | G | 1 | a0001c0008 | 2 | HG00738.hp1 HG01433.hp2 |
synonymous_variant | LOW | c.1413A>G | p.Leu471Leu | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/13 | 1586/4477 | 1413/2562 | 471/853 | chr8 | 55796023 | ||
chr8:55813079
|
T | C | 1 | a0001c0020 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2400T>C | p.Asn800Asn | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/13 | 2573/4477 | 2400/2562 | 800/853 | chr8 | 55813079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55773476
|
C | T | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(32): Show | 335 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(332): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-143C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/13 | chr8 | 55773476 | ||||||
chr8:55773495
|
C | A | 1 | a0001c0001t0014 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/13 | 124 | chr8 | 55773495 | |||||
chr8:55824817
|
G | T | 1 | a0001c0001t0010 | 3 | NA18939.hp2 NA18965.hp1 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*114G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 114 | chr8 | 55824817 | |||||
chr8:55824865
|
G | A | 2 | a0001c0001t0008a0001c0001t0014 | 5 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*162G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 162 | chr8 | 55824865 | |||||
chr8:55825003
|
G | A | 1 | a0001c0001t0015 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 300 | chr8 | 55825003 | |||||
chr8:55825042
|
C | T | 1 | a0003c0003t0005 | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*339C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 339 | chr8 | 55825042 | |||||
chr8:55825081
|
C | T | 1 | a0001c0001t0018 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 378 | chr8 | 55825081 | |||||
chr8:55825425
|
A | C | 2 | a0001c0001t0006a0001c0016t0006 | 7 | HG02523.hp2 NA18946.hp2 NA18950.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*722A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 722 | chr8 | 55825425 | |||||
chr8:55825680
|
A | G | 1 | a0001c0001t0017 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*977A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 977 | chr8 | 55825680 | |||||
chr8:55825697
|
A | G | 27 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(24): Show | 253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*994A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 994 | chr8 | 55825697 | |||||
chr8:55825775
|
GCAA | G | 1 | a0001c0001t0007 | 5 | HG02559.hp2 HG03195.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1074_*1076delAAC | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1074 | INFO_REALIGN_3_PRIME | chr8 | 55825775 | ||||
chr8:55825874
|
C | CT | 8 | a0001c0001t0011a0002c0002t0003a0002c0027t0003others(5): Show | 40 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1185dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1186 | INFO_REALIGN_3_PRIME | chr8 | 55825874 | ||||
chr8:55825892
|
CAG | C | 2 | a0001c0001t0004a0001c0001t0007 | 18 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1192_*1193delAG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1192 | INFO_REALIGN_3_PRIME | chr8 | 55825892 | ||||
chr8:55826127
|
G | A | 1 | a0002c0029t0013 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1424G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1424 | chr8 | 55826127 | |||||
chr8:55826198
|
G | T | 1 | a0008c0011t0016 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1495G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 13/13 | 1495 | chr8 | 55826198 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:55773749
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.101+30C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55773749 | ||||||
chr8:55773764
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.101+45C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55773764 | ||||||
chr8:55773971
|
A | G | 1 | a0002c0002t0003g0324 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.101+252A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55773971 | ||||||
chr8:55774005
|
G | T | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+286G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774005 | ||||||
chr8:55774080
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.101+361C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774080 | ||||||
chr8:55774115
|
A | T | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+396A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774115 | ||||||
chr8:55774253
|
G | A | 1 | a0001c0016t0006g0032 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.101+534G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774253 | ||||||
chr8:55774319
|
G | C | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.101+600G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774319 | ||||||
chr8:55774320
|
C | T | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+601C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774320 | ||||||
chr8:55774356
|
A | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+637A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774356 | ||||||
chr8:55774579
|
G | A | 1 | a0002c0002t0003g0034 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.101+860G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774579 | ||||||
chr8:55774586
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(279): Show | 322 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.101+867G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774586 | ||||||
chr8:55774615
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(278): Show | 321 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.101+896G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774615 | ||||||
chr8:55774708
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(277): Show | 320 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.101+989A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774708 | ||||||
chr8:55774790
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+1071A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774790 | ||||||
chr8:55774801
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(279): Show | 322 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.101+1082T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774801 | ||||||
chr8:55774977
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 5 | HG00408.hp1 HG02165.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1258C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55774977 | ||||||
chr8:55775016
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(279): Show | 322 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.101+1297G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775016 | ||||||
chr8:55775038
|
C | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(278): Show | 321 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.101+1319C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775038 | ||||||
chr8:55775039
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.101+1320C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775039 | ||||||
chr8:55775091
|
A | T | 1 | a0001c0001t0002g0273 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.101+1372A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775091 | ||||||
chr8:55775101
|
A | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(278): Show | 321 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.101+1382A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775101 | ||||||
chr8:55775152
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.101+1433G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775152 | ||||||
chr8:55775155
|
T | G | 17 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0048others(14): Show | 23 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.101+1436T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775155 | ||||||
chr8:55775240
|
GA | G | 129 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(126): Show | 150 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.101+1532delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55775240 | |||||
chr8:55775246
|
AAAAAAG | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(148): Show | 170 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.101+1532_101+1537d others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55775246 | |||||
chr8:55775328
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(287): Show | 330 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(327): Show |
intron_variant | MODIFIER | c.101+1609C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775328 | ||||||
chr8:55775510
|
GAGAA | G | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+1803_101+1806d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55775510 | |||||
chr8:55775667
|
G | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(147): Show | 169 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.101+1948G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775667 | ||||||
chr8:55775900
|
C | T | 1 | a0005c0005t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.101+2181C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775900 | ||||||
chr8:55775962
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+2243G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55775962 | ||||||
chr8:55776026
|
G | T | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.101+2307G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776026 | ||||||
chr8:55776030
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.101+2311A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776030 | ||||||
chr8:55776102
|
C | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0271 | 3 | HG01081.hp1 HG01168.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.101+2383C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776102 | ||||||
chr8:55776173
|
A | G | 11 | a0002c0002t0003g0299a0002c0002t0003g0300a0002c0002t0003g0301others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+2454A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776173 | ||||||
chr8:55776250
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+2531C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776250 | ||||||
chr8:55776277
|
C | CT | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0046others(38): Show | 43 | HG00423.hp2 HG02056.hp1 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.101+2579dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55776277 | |||||
chr8:55776277
|
C | CTT | 7 | a0003c0003t0005g0313a0003c0003t0005g0314a0003c0003t0005g0315others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2578_101+2579d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55776277 | |||||
chr8:55776277
|
CT | C | 12 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0144others(9): Show | 12 | HG01516.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+2579delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55776277 | |||||
chr8:55776358
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 5 | NA18950.hp2 NA18957.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+2639G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776358 | ||||||
chr8:55776362
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.101+2643G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776362 | ||||||
chr8:55776371
|
C | G | 46 | a0001c0001t0001g0126a0002c0002t0003g0029a0002c0002t0003g0034others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.101+2652C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776371 | ||||||
chr8:55776381
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.101+2662C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776381 | ||||||
chr8:55776382
|
G | A | 4 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0280others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+2663G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776382 | ||||||
chr8:55776400
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101+2681C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776400 | ||||||
chr8:55776463
|
A | G | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.101+2744A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776463 | ||||||
chr8:55776610
|
G | C | 1 | a0002c0002t0003g0299 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.101+2891G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776610 | ||||||
chr8:55776675
|
A | C | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.101+2956A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776675 | ||||||
chr8:55776675
|
A | G | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.101+2956A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776675 | ||||||
chr8:55776735
|
T | C | 1 | a0001c0001t0017g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.101+3016T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776735 | ||||||
chr8:55776768
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.101+3049A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776768 | ||||||
chr8:55776794
|
T | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0021others(67): Show | 79 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.101+3075T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776794 | ||||||
chr8:55776799
|
A | C | 1 | a0001c0001t0002g0103 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101+3080A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776799 | ||||||
chr8:55776873
|
T | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+3154T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776873 | ||||||
chr8:55776967
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.101+3248C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776967 | ||||||
chr8:55776980
|
G | C | 1 | a0002c0029t0013g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.101+3261G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55776980 | ||||||
chr8:55777135
|
A | G | 21 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(18): Show | 21 | HG00597.hp2 HG02056.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.101+3416A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777135 | ||||||
chr8:55777289
|
GT | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(261): Show | 297 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.101+3585delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55777289 | |||||
chr8:55777361
|
G | A | 46 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.101+3642G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777361 | ||||||
chr8:55777368
|
C | T | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+3649C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777368 | ||||||
chr8:55777609
|
G | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.101+3890G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777609 | ||||||
chr8:55777662
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.101+3943C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777662 | ||||||
chr8:55777700
|
C | T | 1 | a0002c0002t0003g0295 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.101+3981C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777700 | ||||||
chr8:55777902
|
AT | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(229): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.101+4197delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55777902 | |||||
chr8:55777902
|
ATT | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(47): Show | 54 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(51): Show |
intron_variant | MODIFIER | c.101+4196_101+4197d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55777902 | |||||
chr8:55777904
|
T | A | 48 | a0001c0001t0001g0122a0001c0001t0001g0123a0002c0002t0003g0029others(45): Show | 51 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.101+4185T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777904 | ||||||
chr8:55777905
|
T | A | 89 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(86): Show | 96 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.101+4186T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777905 | ||||||
chr8:55777906
|
T | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(47): Show | 54 | HG00438.hp2 HG00673.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.101+4187T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55777906 | ||||||
chr8:55778101
|
A | T | 1 | a0001c0001t0007g0044 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101+4382A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778101 | ||||||
chr8:55778230
|
G | A | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101+4511G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778230 | ||||||
chr8:55778273
|
TA | T | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-4467delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55778273 | |||||
chr8:55778351
|
A | G | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-4397A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778351 | ||||||
chr8:55778471
|
C | T | 1 | a0017c0019t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.102-4277C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778471 | ||||||
chr8:55778557
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01978.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.102-4191T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778557 | ||||||
chr8:55778567
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.102-4181T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778567 | ||||||
chr8:55778593
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.102-4155A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778593 | ||||||
chr8:55778843
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.102-3905T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778843 | ||||||
chr8:55778874
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.102-3874C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778874 | ||||||
chr8:55778904
|
A | G | 7 | a0001c0001t0001g0191a0001c0001t0006g0192a0001c0001t0006g0193others(4): Show | 7 | HG02523.hp2 NA18946.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-3844A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55778904 | ||||||
chr8:55779018
|
C | T | 2 | a0001c0007t0001g0257a0001c0007t0001g0258 | 2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.102-3730C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779018 | ||||||
chr8:55779197
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.102-3551A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779197 | ||||||
chr8:55779578
|
G | C | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-3170G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779578 | ||||||
chr8:55779605
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG01243.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.102-3143C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55779605 | ||||||
chr8:55779875
|
CT | C | 49 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(46): Show | 52 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.102-2860delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55779875 | |||||
chr8:55780045
|
C | T | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-2703C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780045 | ||||||
chr8:55780160
|
C | CT | 35 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(32): Show | 38 | HG00140.hp1 HG01123.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.102-2573dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780160 | |||||
chr8:55780160
|
CT | C | 95 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0021others(92): Show | 104 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.102-2573delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780160 | |||||
chr8:55780175
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.102-2573T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780175 | ||||||
chr8:55780175
|
T | TTC | 15 | a0002c0002t0003g0292a0002c0002t0003g0293a0002c0002t0003g0294others(12): Show | 15 | HG00639.hp2 HG00741.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.102-2573_102-2572i others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780175 | ||||||
chr8:55780176
|
C | CT | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0053others(20): Show | 25 | HG00673.hp2 HG01109.hp1 HG02135.hp2 others(22): Show |
intron_variant | MODIFIER | c.102-2561dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780176 | |||||
chr8:55780176
|
C | T | 17 | a0001c0001t0001g0188a0002c0002t0003g0292a0002c0002t0003g0293others(14): Show | 17 | HG00639.hp2 HG00741.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.102-2572C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780176 | ||||||
chr8:55780379
|
C | A | 4 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0280others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-2369C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780379 | ||||||
chr8:55780492
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG00621.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.102-2256C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780492 | ||||||
chr8:55780499
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.102-2249C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780499 | ||||||
chr8:55780657
|
C | A | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.102-2091C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780657 | ||||||
chr8:55780663
|
A | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.102-2085A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780663 | ||||||
chr8:55780769
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.102-1979T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780769 | ||||||
chr8:55780906
|
G | C | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102-1842G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55780906 | ||||||
chr8:55780973
|
GT | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0151 | 3 | HG00639.hp1 HG01070.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.102-1772delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55780973 | |||||
chr8:55781090
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102-1658C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781090 | ||||||
chr8:55781148
|
C | T | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.102-1600C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781148 | ||||||
chr8:55781164
|
T | A | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-1584T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781164 | ||||||
chr8:55781370
|
C | A | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-1378C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781370 | ||||||
chr8:55781423
|
ATAAG | A | 2 | a0002c0002t0003g0029a0002c0002t0003g0285 | 3 | HG02486.hp1 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.102-1321_102-1318d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55781423 | |||||
chr8:55781518
|
G | T | 1 | a0001c0001t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.102-1230G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781518 | ||||||
chr8:55781521
|
C | T | 1 | a0017c0019t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.102-1227C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781521 | ||||||
chr8:55781609
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-1139C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781609 | ||||||
chr8:55781847
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-901G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781847 | ||||||
chr8:55781856
|
G | A | 3 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0310 | 3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.102-892G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55781856 | ||||||
chr8:55782079
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.102-669C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782079 | ||||||
chr8:55782146
|
CTTTA | C | 60 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(57): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.102-554_102-551del others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | |||||
chr8:55782146
|
CTTTATTT others(1): Show |
C | 171 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(168): Show | 197 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.102-558_102-551del others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | |||||
chr8:55782146
|
CTTTATTT others(5): Show |
C | 5 | a0001c0001t0001g0016a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 6 | HG02109.hp2 HG02965.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-562_102-551del others(12): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | |||||
chr8:55782146
|
CTTTATTT others(9): Show |
C | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-566_102-551del others(16): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | |||||
chr8:55782146
|
CTTTATTT others(13): Show |
C | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.102-570_102-551del others(20): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | |||||
chr8:55782146
|
CTTTATTT others(17): Show |
C | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-574_102-551del others(24): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 55782146 | |||||
chr8:55782149
|
T | A | 11 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(8): Show | 11 | HG02976.hp1 NA18944.hp2 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.102-599T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782149 | ||||||
chr8:55782151
|
T | A | 1 | a0001c0001t0002g0061 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.102-597T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782151 | ||||||
chr8:55782153
|
T | A | 44 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(41): Show | 47 | HG00438.hp2 HG00673.hp2 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.102-595T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782153 | ||||||
chr8:55782157
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(162): Show | 191 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.102-591T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782157 | ||||||
chr8:55782161
|
T | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0048others(2): Show | 6 | HG02109.hp2 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-587T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782161 | ||||||
chr8:55782165
|
T | A | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.102-583T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782165 | ||||||
chr8:55782169
|
T | A | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.102-579T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782169 | ||||||
chr8:55782173
|
T | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-575T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782173 | ||||||
chr8:55782221
|
G | A | 1 | a0001c0014t0001g0154 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.102-527G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782221 | ||||||
chr8:55782222
|
C | T | 1 | a0002c0002t0003g0297 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.102-526C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782222 | ||||||
chr8:55782295
|
C | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.102-453C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782295 | ||||||
chr8:55782298
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.102-450C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782298 | ||||||
chr8:55782312
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02027.hp1 NA18966.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-436G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782312 | ||||||
chr8:55782338
|
C | T | 1 | a0001c0007t0001g0270 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.102-410C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782338 | ||||||
chr8:55782610
|
G | A | 3 | a0002c0002t0003g0300a0002c0002t0003g0301a0002c0027t0003g0302 | 3 | HG00639.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.102-138G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782610 | ||||||
chr8:55782707
|
C | T | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-41C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782707 | ||||||
chr8:55782743
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0190 | 2 | HG04115.hp1 HG04228.hp1 |
splice_region_variant&intron_variant | LOW | c.102-5C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 1/12 | chr8 | 55782743 | ||||||
chr8:55783215
|
A | T | 1 | a0001c0001t0010g0236 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.166+403A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783215 | ||||||
chr8:55783216
|
C | G | 1 | a0001c0001t0010g0236 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.166+404C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783216 | ||||||
chr8:55783454
|
T | G | 1 | a0001c0001t0001g0024 | 2 | NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.166+642T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783454 | ||||||
chr8:55783572
|
A | G | 1 | a0001c0008t0001g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.166+760A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783572 | ||||||
chr8:55783825
|
T | G | 1 | a0001c0001t0008g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.166+1013T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55783825 | ||||||
chr8:55784036
|
C | T | 90 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(87): Show | 97 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.166+1224C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784036 | ||||||
chr8:55784096
|
C | A | 3 | a0002c0002t0003g0286a0006c0006t0003g0010a0006c0006t0003g0296 | 5 | HG02145.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.166+1284C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784096 | ||||||
chr8:55784137
|
A | G | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.166+1325A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784137 | ||||||
chr8:55784167
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(148): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.166+1355G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784167 | ||||||
chr8:55784343
|
T | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.167-1376T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784343 | ||||||
chr8:55784630
|
A | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.167-1089A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784630 | ||||||
chr8:55784997
|
C | T | 46 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.167-722C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55784997 | ||||||
chr8:55785058
|
G | GT | 4 | a0002c0002t0003g0299a0002c0002t0003g0307a0006c0006t0003g0296others(1): Show | 4 | HG02145.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-655dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 55785058 | |||||
chr8:55785065
|
G | T | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.167-654G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785065 | ||||||
chr8:55785071
|
TG | T | 9 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.167-647delG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785071 | ||||||
chr8:55785072
|
G | T | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.167-647G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785072 | ||||||
chr8:55785138
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.167-581C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785138 | ||||||
chr8:55785244
|
CG | C | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.167-472delG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 55785244 | |||||
chr8:55785365
|
T | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.167-354T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785365 | ||||||
chr8:55785371
|
TTTTG | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0197a0001c0001t0001g0263others(3): Show | 7 | HG03669.hp2 NA18944.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.167-336_167-333del others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 55785371 | |||||
chr8:55785379
|
G | T | 1 | a0005c0005t0009g0280 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.167-340G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785379 | ||||||
chr8:55785416
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.167-303C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785416 | ||||||
chr8:55785452
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG02129.hp1 NA18986.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.167-267C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785452 | ||||||
chr8:55785480
|
G | C | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.167-239G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785480 | ||||||
chr8:55785490
|
G | A | 46 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.167-229G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785490 | ||||||
chr8:55785515
|
T | C | 1 | a0002c0002t0003g0297 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.167-204T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 2/12 | chr8 | 55785515 | ||||||
chr8:55785929
|
G | A | 2 | a0001c0007t0001g0257a0001c0007t0001g0270 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.339+38G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 3/12 | chr8 | 55785929 | ||||||
chr8:55787087
|
C | A | 4 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0280others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+27C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787087 | ||||||
chr8:55787222
|
C | A | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1162+162C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787222 | ||||||
chr8:55787231
|
TTAA | T | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+175_1162+177d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55787231 | |||||
chr8:55787302
|
A | G | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1162+242A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787302 | ||||||
chr8:55787423
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1162+363G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787423 | ||||||
chr8:55787434
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1162+374A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787434 | ||||||
chr8:55787605
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162+545G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787605 | ||||||
chr8:55787626
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1162+566C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787626 | ||||||
chr8:55787769
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1162+709C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787769 | ||||||
chr8:55787891
|
G | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1162+831G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787891 | ||||||
chr8:55787894
|
C | A | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+834C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787894 | ||||||
chr8:55787895
|
A | G | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+835A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787895 | ||||||
chr8:55787896
|
A | C | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+836A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787896 | ||||||
chr8:55787897
|
G | A | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1162+837G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787897 | ||||||
chr8:55787909
|
A | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1162+849A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787909 | ||||||
chr8:55787981
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1162+921G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55787981 | ||||||
chr8:55788114
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1162+1054G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788114 | ||||||
chr8:55788151
|
A | T | 3 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0310 | 3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1162+1091A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788151 | ||||||
chr8:55788235
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1162+1175C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788235 | ||||||
chr8:55788278
|
TAAC | T | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1162+1221_1162+122 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55788278 | |||||
chr8:55788353
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1162+1293G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788353 | ||||||
chr8:55788376
|
A | C | 16 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(13): Show | 22 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1162+1316A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788376 | ||||||
chr8:55788399
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1162+1339G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788399 | ||||||
chr8:55788454
|
C | CTTT | 27 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(24): Show | 28 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1162+1411_1162+141 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55788454 | |||||
chr8:55788454
|
CT | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(178): Show | 207 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1162+1413delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 55788454 | |||||
chr8:55788548
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1162+1488G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788548 | ||||||
chr8:55788607
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1162+1547C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788607 | ||||||
chr8:55788664
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1163-1518G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788664 | ||||||
chr8:55788710
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1163-1472C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788710 | ||||||
chr8:55788790
|
T | C | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163-1392T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788790 | ||||||
chr8:55788889
|
A | T | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1163-1293A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788889 | ||||||
chr8:55788943
|
G | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1163-1239G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55788943 | ||||||
chr8:55789061
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1163-1121T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789061 | ||||||
chr8:55789263
|
A | G | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0020t0001g0183 | 3 | HG01175.hp2 HG02145.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1163-919A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789263 | ||||||
chr8:55789332
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1163-850T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789332 | ||||||
chr8:55789423
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1163-759C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789423 | ||||||
chr8:55789424
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1163-758G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789424 | ||||||
chr8:55789500
|
A | G | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1163-682A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789500 | ||||||
chr8:55789592
|
C | G | 1 | a0013c0013t0001g0180 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1163-590C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789592 | ||||||
chr8:55789666
|
G | A | 3 | a0001c0001t0010g0209a0001c0001t0010g0236a0001c0001t0010g0268 | 3 | NA18939.hp2 NA18965.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1163-516G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789666 | ||||||
chr8:55789993
|
A | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1163-189A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55789993 | ||||||
chr8:55790000
|
A | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1163-182A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55790000 | ||||||
chr8:55790007
|
T | A | 1 | a0020c0024t0001g0139 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1163-175T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 4/12 | chr8 | 55790007 | ||||||
chr8:55790470
|
C | T | 1 | a0019c0023t0001g0322 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1280+171C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790470 | ||||||
chr8:55790504
|
CT | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(260): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.1280+220delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790504 | |||||
chr8:55790588
|
A | C | 1 | a0020c0024t0001g0139 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1280+289A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790588 | ||||||
chr8:55790597
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1280+298C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790597 | ||||||
chr8:55790682
|
A | C | 1 | a0020c0024t0001g0139 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1280+383A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790682 | ||||||
chr8:55790706
|
A | G | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+407A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790706 | ||||||
chr8:55790708
|
A | G | 4 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0280others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1280+409A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790708 | ||||||
chr8:55790716
|
G | A | 1 | a0001c0001t0002g0128 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1280+417G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790716 | ||||||
chr8:55790733
|
G | A | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+434G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790733 | ||||||
chr8:55790750
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0020others(44): Show | 57 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1280+451C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790750 | ||||||
chr8:55790760
|
C | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(148): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1280+461C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790760 | ||||||
chr8:55790803
|
G | A | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1280+504G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55790803 | ||||||
chr8:55790966
|
T | TTC | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(164): Show | 190 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1280+688_1280+689d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | |||||
chr8:55790966
|
T | TTCTC | 26 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0055others(23): Show | 33 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1280+686_1280+689d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | |||||
chr8:55790966
|
T | TTCTCTC | 22 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(19): Show | 22 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1280+684_1280+689d others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | |||||
chr8:55790966
|
TTCTC | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.1280+686_1280+689d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | |||||
chr8:55790966
|
TTCTCTCT others(1): Show |
T | 6 | a0001c0001t0001g0033a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280+682_1280+689d others(10): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 55790966 | |||||
chr8:55791055
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1280+756C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791055 | ||||||
chr8:55791319
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280+1020G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791319 | ||||||
chr8:55791525
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1281-1173T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791525 | ||||||
chr8:55791618
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1281-1080C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791618 | ||||||
chr8:55791766
|
T | C | 35 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(32): Show | 38 | HG00140.hp1 HG00639.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1281-932T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791766 | ||||||
chr8:55791790
|
A | C | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1281-908A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791790 | ||||||
chr8:55791792
|
A | T | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1281-906A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791792 | ||||||
chr8:55791848
|
T | C | 14 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0004g0002others(11): Show | 20 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1281-850T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791848 | ||||||
chr8:55791861
|
G | A | 3 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0310 | 3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1281-837G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791861 | ||||||
chr8:55791930
|
A | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1281-768A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791930 | ||||||
chr8:55791953
|
A | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1281-745A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791953 | ||||||
chr8:55791980
|
A | T | 3 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323 | 3 | HG01192.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1281-718A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791980 | ||||||
chr8:55791996
|
G | A | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1281-702G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55791996 | ||||||
chr8:55792000
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1281-698A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792000 | ||||||
chr8:55792027
|
T | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1281-671T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792027 | ||||||
chr8:55792089
|
A | G | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1281-609A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792089 | ||||||
chr8:55792102
|
G | A | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1281-596G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792102 | ||||||
chr8:55792105
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1281-593C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792105 | ||||||
chr8:55792106
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1281-592G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792106 | ||||||
chr8:55792244
|
G | C | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1281-454G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792244 | ||||||
chr8:55792364
|
G | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0213others(5): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1281-334G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792364 | ||||||
chr8:55792439
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1281-259C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792439 | ||||||
chr8:55792593
|
G | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281-105G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792593 | ||||||
chr8:55792632
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1281-66A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 5/12 | chr8 | 55792632 | ||||||
chr8:55792879
|
G | A | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1367+95G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55792879 | ||||||
chr8:55792893
|
T | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0075a0001c0001t0002g0076others(3): Show | 7 | HG01081.hp2 HG01358.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367+109T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55792893 | ||||||
chr8:55793017
|
C | G | 5 | a0005c0005t0002g0309a0005c0005t0009g0278a0005c0005t0009g0279others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+233C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793017 | ||||||
chr8:55793103
|
C | G | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1367+319C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793103 | ||||||
chr8:55793169
|
A | G | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1367+385A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793169 | ||||||
chr8:55793259
|
A | G | 46 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1367+475A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793259 | ||||||
chr8:55793416
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1367+632C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793416 | ||||||
chr8:55793458
|
C | T | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1367+674C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793458 | ||||||
chr8:55793495
|
A | G | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+711A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793495 | ||||||
chr8:55793535
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1367+751T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793535 | ||||||
chr8:55793556
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1367+772A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793556 | ||||||
chr8:55793579
|
GT | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+801delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793579 | |||||
chr8:55793653
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1367+869C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793653 | ||||||
chr8:55793694
|
A | G | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1367+910A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793694 | ||||||
chr8:55793722
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1367+938C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793722 | ||||||
chr8:55793733
|
A | AATTT | 26 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0107others(23): Show | 27 | HG01243.hp2 HG02071.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.1367+990_1367+993d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | |||||
chr8:55793733
|
AATTT | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0033others(42): Show | 50 | HG00639.hp2 HG00741.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.1367+990_1367+993d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | |||||
chr8:55793733
|
AATTTATT others(1): Show |
A | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0055others(5): Show | 8 | HG00642.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+986_1367+993d others(10): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | |||||
chr8:55793733
|
AATTTATT others(5): Show |
A | 23 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0058others(20): Show | 30 | HG00323.hp1 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1367+982_1367+993d others(14): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | |||||
chr8:55793733
|
AATTTATT others(9): Show |
A | 9 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367+978_1367+993d others(18): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55793733 | |||||
chr8:55793762
|
A | T | 1 | a0005c0005t0009g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1367+978A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793762 | ||||||
chr8:55793766
|
A | T | 3 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0310 | 3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1367+982A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793766 | ||||||
chr8:55793770
|
A | T | 5 | a0005c0005t0002g0309a0005c0005t0009g0278a0005c0005t0009g0279others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+986A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793770 | ||||||
chr8:55793774
|
A | T | 5 | a0005c0005t0002g0309a0005c0005t0009g0278a0005c0005t0009g0279others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+990A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793774 | ||||||
chr8:55793810
|
G | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1367+1026G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793810 | ||||||
chr8:55793864
|
C | T | 2 | a0001c0001t0008g0207a0001c0001t0014g0210 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1367+1080C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793864 | ||||||
chr8:55793866
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1367+1082C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793866 | ||||||
chr8:55793919
|
C | T | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1367+1135C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793919 | ||||||
chr8:55793925
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1367+1141C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793925 | ||||||
chr8:55793928
|
A | G | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1367+1144A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55793928 | ||||||
chr8:55794006
|
A | G | 16 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(13): Show | 22 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1367+1222A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794006 | ||||||
chr8:55794070
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+1286G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794070 | ||||||
chr8:55794175
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1367+1391T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794175 | ||||||
chr8:55794213
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1367+1429T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794213 | ||||||
chr8:55794390
|
A | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1368-1588A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794390 | ||||||
chr8:55794426
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1368-1552C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794426 | ||||||
chr8:55794435
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(175): Show | 204 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1368-1543G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794435 | ||||||
chr8:55794542
|
T | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1368-1436T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794542 | ||||||
chr8:55794644
|
T | G | 1 | a0001c0001t0001g0219 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1368-1334T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794644 | ||||||
chr8:55794796
|
C | T | 1 | a0002c0002t0003g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1368-1182C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794796 | ||||||
chr8:55794864
|
T | C | 1 | a0002c0002t0003g0295 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1368-1114T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794864 | ||||||
chr8:55794872
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1368-1106A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794872 | ||||||
chr8:55794915
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1368-1063A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55794915 | ||||||
chr8:55795102
|
G | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1368-876G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795102 | ||||||
chr8:55795209
|
C | A | 1 | a0019c0023t0001g0322 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1368-769C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795209 | ||||||
chr8:55795245
|
T | C | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1368-733T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795245 | ||||||
chr8:55795530
|
T | C | 3 | a0001c0001t0002g0101a0001c0001t0002g0273a0012c0025t0002g0089 | 3 | HG00597.hp1 HG02027.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1368-448T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795530 | ||||||
chr8:55795612
|
A | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1368-366A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795612 | ||||||
chr8:55795672
|
CGTTT | C | 4 | a0001c0001t0010g0209a0001c0001t0010g0236a0001c0001t0010g0268others(1): Show | 4 | HG01123.hp2 NA18939.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-289_1368-286d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55795672 | |||||
chr8:55795824
|
G | C | 1 | a0002c0002t0003g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1368-154G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | chr8 | 55795824 | ||||||
chr8:55795970
|
T | TG | 46 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
splice_region_variant&intron_variant | LOW | c.1368-7dupG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 55795970 | |||||
chr8:55796345
|
G | A | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+193G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796345 | ||||||
chr8:55796374
|
G | A | 3 | a0001c0001t0004g0002a0001c0001t0004g0038a0001c0001t0004g0045 | 6 | HG00323.hp1 HG01255.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542+222G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796374 | ||||||
chr8:55796476
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1542+324G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796476 | ||||||
chr8:55796523
|
T | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0024others(36): Show | 47 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1542+371T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796523 | ||||||
chr8:55796526
|
T | C | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542+374T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796526 | ||||||
chr8:55796577
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1542+425A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796577 | ||||||
chr8:55796603
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0267 | 2 | HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1542+451G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796603 | ||||||
chr8:55796642
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1542+490C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796642 | ||||||
chr8:55796656
|
T | C | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1542+504T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796656 | ||||||
chr8:55796712
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+560C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796712 | ||||||
chr8:55796731
|
C | G | 1 | a0002c0002t0003g0295 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1542+579C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796731 | ||||||
chr8:55796884
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1542+732G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796884 | ||||||
chr8:55796943
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1542+791A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55796943 | ||||||
chr8:55797012
|
A | G | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1542+860A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797012 | ||||||
chr8:55797058
|
G | C | 11 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(8): Show | 14 | HG01123.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1542+906G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797058 | ||||||
chr8:55797339
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1542+1187C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797339 | ||||||
chr8:55797571
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-1343G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797571 | ||||||
chr8:55797616
|
G | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1543-1298G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797616 | ||||||
chr8:55797789
|
A | T | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1543-1125A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797789 | ||||||
chr8:55797977
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1543-937C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55797977 | ||||||
chr8:55798069
|
A | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1543-845A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798069 | ||||||
chr8:55798122
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-792A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798122 | ||||||
chr8:55798219
|
C | T | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1543-695C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798219 | ||||||
chr8:55798426
|
C | T | 4 | a0003c0003t0005g0316a0003c0003t0005g0317a0003c0003t0005g0318others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-488C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798426 | ||||||
chr8:55798468
|
G | A | 1 | a0009c0010t0001g0030 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1543-446G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798468 | ||||||
chr8:55798502
|
A | G | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1543-412A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798502 | ||||||
chr8:55798708
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(157): Show | 180 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1543-206A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798708 | ||||||
chr8:55798777
|
CT | C | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1543-135delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 55798777 | |||||
chr8:55798822
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1543-92G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798822 | ||||||
chr8:55798890
|
C | T | 28 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0052others(25): Show | 31 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.1543-24C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 7/12 | chr8 | 55798890 | ||||||
chr8:55799454
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0151a0001c0001t0001g0163others(1): Show | 5 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849+234G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799454 | ||||||
chr8:55799457
|
G | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1849+237G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799457 | ||||||
chr8:55799662
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1849+442T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799662 | ||||||
chr8:55799672
|
G | T | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1849+452G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799672 | ||||||
chr8:55799813
|
G | A | 46 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1849+593G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799813 | ||||||
chr8:55799842
|
G | A | 1 | a0003c0003t0005g0313 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1849+622G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799842 | ||||||
chr8:55799885
|
T | A | 1 | a0001c0001t0002g0063 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1849+665T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799885 | ||||||
chr8:55799954
|
T | C | 4 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0280others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1849+734T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799954 | ||||||
chr8:55799955
|
A | T | 1 | a0001c0001t0001g0216 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1849+735A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55799955 | ||||||
chr8:55800174
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1849+954T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800174 | ||||||
chr8:55800235
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1849+1015A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800235 | ||||||
chr8:55800275
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0151a0001c0001t0001g0163 | 4 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849+1055G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800275 | ||||||
chr8:55800282
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1849+1062A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800282 | ||||||
chr8:55800510
|
A | G | 2 | a0001c0001t0002g0097a0014c0015t0002g0311 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1849+1290A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800510 | ||||||
chr8:55800617
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1849+1397C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800617 | ||||||
chr8:55800686
|
A | G | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1849+1466A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55800686 | ||||||
chr8:55801057
|
A | G | 7 | a0003c0003t0005g0312a0003c0003t0005g0314a0003c0003t0005g0315others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1850-1400A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801057 | ||||||
chr8:55801134
|
T | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1850-1323T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801134 | ||||||
chr8:55801241
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1850-1216A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801241 | ||||||
chr8:55801433
|
G | A | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1850-1024G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801433 | ||||||
chr8:55801445
|
AT | A | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1850-1003delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801445 | |||||
chr8:55801449
|
TTTTTTAG others(307): Show |
T | 1 | a0001c0001t0001g0016 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1850-990_1850-677d others(2): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801449 | |||||
chr8:55801565
|
C | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1850-892C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801565 | ||||||
chr8:55801581
|
T | TC | 22 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(19): Show | 23 | HG00140.hp1 HG00741.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1850-875dupC | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801581 | |||||
chr8:55801582
|
C | CCT | 7 | a0002c0002t0003g0286a0002c0002t0003g0300a0002c0002t0003g0301others(4): Show | 9 | HG00639.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1850-875_1850-874i others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CCTT | 5 | a0002c0029t0013g0283a0005c0005t0002g0309a0005c0005t0009g0278others(2): Show | 5 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1850-875_1850-874i others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CCTTTTTT others(15): Show |
1 | a0003c0003t0005g0313 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1850-875_1850-874i others(24): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CCTTTTTT others(18): Show |
1 | a0003c0003t0005g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1850-875_1850-874i others(27): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CCTTTTTT others(20): Show |
1 | a0003c0003t0005g0317 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1850-875_1850-874i others(29): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CCTTTTTT others(21): Show |
2 | a0003c0003t0005g0314a0003c0003t0005g0318 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1850-875_1850-874i others(30): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CCTTTTTT others(23): Show |
2 | a0003c0003t0005g0312a0003c0003t0005g0315 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1850-875_1850-874i others(32): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CCTTTTTT others(25): Show |
1 | a0003c0003t0005g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1850-875_1850-874i others(34): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801582 | ||||||
chr8:55801582
|
C | CT | 52 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(49): Show | 56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1850-851dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | |||||
chr8:55801582
|
C | CTT | 128 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(125): Show | 146 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1850-852_1850-851d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | |||||
chr8:55801582
|
C | CTTT | 24 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0117others(21): Show | 24 | HG01175.hp1 HG01358.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1850-853_1850-851d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | |||||
chr8:55801582
|
CTTTTTTT others(3): Show |
C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1850-860_1850-851d others(12): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 55801582 | |||||
chr8:55801583
|
T | C | 1 | a0002c0002t0003g0287 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1850-874T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801583 | ||||||
chr8:55801644
|
A | G | 1 | a0002c0002t0003g0297 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1850-813A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801644 | ||||||
chr8:55801674
|
C | T | 20 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(17): Show | 20 | HG01109.hp1 HG01243.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1850-783C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801674 | ||||||
chr8:55801689
|
C | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0173others(3): Show | 6 | HG01175.hp1 HG01358.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1850-768C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801689 | ||||||
chr8:55801741
|
A | G | 1 | a0001c0007t0001g0258 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1850-716A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801741 | ||||||
chr8:55801885
|
T | A | 1 | a0001c0001t0002g0065 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1850-572T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55801885 | ||||||
chr8:55802022
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1850-435G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802022 | ||||||
chr8:55802051
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1850-406G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802051 | ||||||
chr8:55802055
|
G | A | 10 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(7): Show | 13 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1850-402G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802055 | ||||||
chr8:55802062
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1850-395C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802062 | ||||||
chr8:55802066
|
C | T | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.1850-391C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802066 | ||||||
chr8:55802125
|
C | T | 1 | a0001c0001t0002g0061 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1850-332C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802125 | ||||||
chr8:55802233
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1850-224G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802233 | ||||||
chr8:55802302
|
T | C | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1850-155T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802302 | ||||||
chr8:55802412
|
A | G | 2 | a0001c0001t0004g0005a0001c0001t0004g0043 | 4 | HG01192.hp2 HG01261.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1850-45A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 8/12 | chr8 | 55802412 | ||||||
chr8:55802624
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0151a0001c0001t0001g0163others(1): Show | 5 | HG00639.hp1 HG01070.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1999+18T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802624 | ||||||
chr8:55802666
|
G | A | 1 | a0003c0003t0005g0313 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1999+60G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802666 | ||||||
chr8:55802737
|
G | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1999+131G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802737 | ||||||
chr8:55802913
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1999+307A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802913 | ||||||
chr8:55802918
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1999+312A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802918 | ||||||
chr8:55802941
|
C | G | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1999+335C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802941 | ||||||
chr8:55802952
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1999+346C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55802952 | ||||||
chr8:55802961
|
GT | G | 32 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(29): Show | 35 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1999+365delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55802961 | |||||
chr8:55803000
|
C | G | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.1999+394C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803000 | ||||||
chr8:55803001
|
G | A | 1 | a0004c0004t0001g0185 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1999+395G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803001 | ||||||
chr8:55803068
|
G | A | 1 | a0019c0023t0001g0322 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1999+462G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803068 | ||||||
chr8:55803124
|
TGG | T | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1999+524_1999+525d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803124 | |||||
chr8:55803130
|
G | GGT | 49 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(46): Show | 53 | HG00673.hp2 HG01109.hp1 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.1999+543_1999+544d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803130 | |||||
chr8:55803130
|
G | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0021others(112): Show | 130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1999+524G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803130 | ||||||
chr8:55803132
|
T | G | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1999+526T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803132 | ||||||
chr8:55803235
|
A | G | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.1999+629A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803235 | ||||||
chr8:55803356
|
C | G | 1 | a0001c0008t0001g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1999+750C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803356 | ||||||
chr8:55803414
|
T | C | 4 | a0003c0003t0005g0316a0003c0003t0005g0317a0003c0003t0005g0318others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1999+808T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803414 | ||||||
chr8:55803439
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1999+833A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803439 | ||||||
chr8:55803520
|
G | C | 3 | a0002c0002t0003g0292a0002c0002t0003g0293a0002c0002t0003g0298 | 3 | HG02896.hp2 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1999+914G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803520 | ||||||
chr8:55803538
|
G | A | 13 | a0001c0001t0001g0046a0001c0001t0004g0002a0001c0001t0004g0005others(10): Show | 19 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1999+932G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803538 | ||||||
chr8:55803543
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1999+937A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803543 | ||||||
chr8:55803629
|
A | T | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1999+1023A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803629 | ||||||
chr8:55803692
|
C | CT | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0130others(10): Show | 14 | HG02129.hp1 NA18945.hp2 NA18957.hp1 others(11): Show |
intron_variant | MODIFIER | c.1999+1097dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803692 | |||||
chr8:55803692
|
CT | C | 46 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1999+1097delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55803692 | |||||
chr8:55803809
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0172 | 3 | NA18971.hp2 NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2000-1084C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803809 | ||||||
chr8:55803872
|
C | T | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2000-1021C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803872 | ||||||
chr8:55803931
|
C | T | 1 | a0001c0001t0018g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2000-962C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803931 | ||||||
chr8:55803932
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000-961G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803932 | ||||||
chr8:55803940
|
C | G | 3 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0072 | 3 | HG02071.hp1 HG02523.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2000-953C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55803940 | ||||||
chr8:55804041
|
A | G | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2000-852A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804041 | ||||||
chr8:55804372
|
C | T | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2000-521C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804372 | ||||||
chr8:55804401
|
G | A | 2 | a0001c0001t0001g0191a0001c0007t0001g0257 | 2 | NA19056.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2000-492G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804401 | ||||||
chr8:55804529
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2000-364C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804529 | ||||||
chr8:55804654
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000-239A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804654 | ||||||
chr8:55804726
|
A | G | 1 | a0003c0003t0005g0315 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2000-167A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804726 | ||||||
chr8:55804776
|
TA | T | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2000-112delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 55804776 | |||||
chr8:55804837
|
G | T | 8 | a0002c0002t0003g0034a0002c0002t0003g0281a0002c0002t0003g0286others(5): Show | 10 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2000-56G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804837 | ||||||
chr8:55804876
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2000-17A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 9/12 | chr8 | 55804876 | ||||||
chr8:55805088
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2143+52A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805088 | ||||||
chr8:55805171
|
C | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+135C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805171 | ||||||
chr8:55805396
|
C | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | NA18939.hp1 NA19072.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2143+360C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805396 | ||||||
chr8:55805462
|
A | C | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2143+426A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805462 | ||||||
chr8:55805683
|
C | G | 3 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323 | 3 | HG01192.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2143+647C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805683 | ||||||
chr8:55805775
|
A | G | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+739A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805775 | ||||||
chr8:55805831
|
G | A | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2143+795G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805831 | ||||||
chr8:55805881
|
TA | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(152): Show | 181 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2143+868delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | |||||
chr8:55805881
|
TAA | T | 22 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(19): Show | 22 | HG00323.hp2 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2143+867_2143+868d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | |||||
chr8:55805881
|
TAAAA | T | 9 | a0001c0001t0001g0055a0003c0003t0005g0312a0003c0003t0005g0313others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2143+865_2143+868d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | |||||
chr8:55805881
|
TAAAAA | T | 33 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(30): Show | 36 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.2143+864_2143+868d others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805881 | |||||
chr8:55805903
|
A | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2143+867A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805903 | ||||||
chr8:55805906
|
T | G | 1 | a0001c0001t0002g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2143+870T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805906 | ||||||
chr8:55805923
|
G | A | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+887G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805923 | ||||||
chr8:55805961
|
AGATGAGA others(1): Show |
A | 26 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0145others(23): Show | 30 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.2143+931_2143+938d others(10): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55805961 | |||||
chr8:55805962
|
G | C | 1 | a0001c0001t0002g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2143+926G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805962 | ||||||
chr8:55805997
|
T | C | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+961T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55805997 | ||||||
chr8:55806042
|
G | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+1006G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806042 | ||||||
chr8:55806077
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2143+1041C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806077 | ||||||
chr8:55806114
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2143+1078A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806114 | ||||||
chr8:55806225
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2143+1189G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806225 | ||||||
chr8:55806356
|
C | CA | 60 | a0001c0001t0001g0046a0001c0001t0001g0106a0001c0001t0001g0133others(57): Show | 63 | HG00140.hp1 HG00423.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2143+1341dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806356 | |||||
chr8:55806356
|
C | CAA | 13 | a0001c0008t0001g0175a0002c0002t0003g0290a0002c0002t0003g0307others(10): Show | 13 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.2143+1340_2143+134 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806356 | |||||
chr8:55806356
|
CA | C | 8 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 10 | HG01192.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.2143+1341delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806356 | |||||
chr8:55806385
|
GA | G | 46 | a0001c0001t0002g0084a0002c0002t0003g0029a0002c0002t0003g0034others(43): Show | 49 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.2143+1360delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806385 | |||||
chr8:55806640
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2143+1604A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806640 | ||||||
chr8:55806851
|
T | C | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+1815T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806851 | ||||||
chr8:55806871
|
C | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(147): Show | 169 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.2143+1835C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806871 | ||||||
chr8:55806899
|
T | C | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2143+1863T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806899 | ||||||
chr8:55806924
|
A | T | 1 | a0001c0001t0001g0199 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2143+1888A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806924 | ||||||
chr8:55806936
|
C | CT | 17 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0048others(14): Show | 23 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.2143+1909dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55806936 | |||||
chr8:55806937
|
T | C | 1 | a0002c0002t0003g0286 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2143+1901T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806937 | ||||||
chr8:55806951
|
G | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2143+1915G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806951 | ||||||
chr8:55806959
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2143+1923A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55806959 | ||||||
chr8:55807506
|
G | GT | 41 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0024others(38): Show | 48 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.2143+2483dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55807506 | |||||
chr8:55807506
|
G | GTT | 9 | a0001c0001t0001g0028a0001c0001t0001g0189a0001c0001t0001g0219others(6): Show | 10 | HG00408.hp1 HG01978.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.2143+2482_2143+248 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55807506 | |||||
chr8:55807506
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2143+2470G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55807506 | ||||||
chr8:55807770
|
A | G | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2143+2734A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55807770 | ||||||
chr8:55807874
|
T | G | 9 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0077others(6): Show | 12 | HG01123.hp1 HG01975.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.2143+2838T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55807874 | ||||||
chr8:55808033
|
C | G | 1 | a0002c0002t0003g0299 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2144-2848C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808033 | ||||||
chr8:55808070
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2144-2811C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808070 | ||||||
chr8:55808143
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2144-2738A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808143 | ||||||
chr8:55808356
|
A | C | 21 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(18): Show | 21 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2144-2525A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808356 | ||||||
chr8:55808394
|
G | A | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2144-2487G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808394 | ||||||
chr8:55808470
|
C | T | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-2411C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808470 | ||||||
chr8:55808511
|
CT | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(251): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.2144-2355delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55808511 | |||||
chr8:55808757
|
A | G | 1 | a0002c0029t0013g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2144-2124A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808757 | ||||||
chr8:55808762
|
G | A | 7 | a0003c0003t0005g0312a0003c0003t0005g0314a0003c0003t0005g0315others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2144-2119G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808762 | ||||||
chr8:55808921
|
A | G | 2 | a0001c0001t0001g0256a0001c0007t0001g0258 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2144-1960A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55808921 | ||||||
chr8:55809038
|
A | G | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2144-1843A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809038 | ||||||
chr8:55809056
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(175): Show | 204 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.2144-1825G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809056 | ||||||
chr8:55809128
|
C | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0020t0001g0183 | 3 | HG01175.hp2 HG02145.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2144-1753C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809128 | ||||||
chr8:55809194
|
T | A | 1 | a0004c0004t0001g0035 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2144-1687T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809194 | ||||||
chr8:55809312
|
C | G | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2144-1569C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809312 | ||||||
chr8:55809384
|
C | T | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2144-1497C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809384 | ||||||
chr8:55809453
|
A | AT | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(159): Show | 181 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.2144-1414dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55809453 | |||||
chr8:55809491
|
C | A | 1 | a0017c0019t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2144-1390C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809491 | ||||||
chr8:55809497
|
G | T | 1 | a0001c0001t0001g0259 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2144-1384G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809497 | ||||||
chr8:55809619
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2144-1262G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809619 | ||||||
chr8:55809666
|
C | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0179 | 3 | HG00408.hp2 NA18987.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2144-1215C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809666 | ||||||
chr8:55809682
|
G | A | 1 | a0002c0002t0003g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2144-1199G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809682 | ||||||
chr8:55809725
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2144-1156G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809725 | ||||||
chr8:55809797
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-1084G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809797 | ||||||
chr8:55809879
|
TATC | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2144-997_2144-995d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 55809879 | |||||
chr8:55809957
|
AC | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0020t0001g0183 | 3 | HG01175.hp2 HG02145.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2144-923delC | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55809957 | ||||||
chr8:55810016
|
A | G | 32 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(29): Show | 35 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2144-865A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810016 | ||||||
chr8:55810116
|
A | G | 2 | a0001c0001t0006g0193a0001c0001t0006g0194 | 2 | NA18950.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2144-765A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810116 | ||||||
chr8:55810132
|
C | T | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2144-749C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810132 | ||||||
chr8:55810166
|
A | G | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2144-715A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810166 | ||||||
chr8:55810168
|
A | G | 1 | a0001c0001t0004g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2144-713A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810168 | ||||||
chr8:55810301
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2144-580C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810301 | ||||||
chr8:55810316
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2144-565A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810316 | ||||||
chr8:55810332
|
C | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-549C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810332 | ||||||
chr8:55810438
|
A | G | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2144-443A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810438 | ||||||
chr8:55810448
|
G | A | 17 | a0002c0002t0003g0292a0002c0002t0003g0293a0002c0002t0003g0294others(14): Show | 17 | HG00639.hp2 HG00741.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2144-433G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810448 | ||||||
chr8:55810467
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2144-414G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810467 | ||||||
chr8:55810496
|
T | A | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2144-385T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810496 | ||||||
chr8:55810547
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2144-334A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810547 | ||||||
chr8:55810719
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(148): Show | 170 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2144-162A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810719 | ||||||
chr8:55810818
|
A | G | 5 | a0001c0001t0007g0039a0001c0001t0007g0040a0001c0001t0007g0041others(2): Show | 5 | HG02559.hp2 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2144-63A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810818 | ||||||
chr8:55810825
|
C | T | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-56C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 10/12 | chr8 | 55810825 | ||||||
chr8:55811260
|
C | T | 13 | a0001c0001t0001g0046a0001c0001t0004g0002a0001c0001t0004g0005others(10): Show | 19 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.2360+163C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811260 | ||||||
chr8:55811261
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2360+164G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811261 | ||||||
chr8:55811561
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2360+464A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811561 | ||||||
chr8:55811571
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2360+474C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811571 | ||||||
chr8:55811596
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2360+499C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811596 | ||||||
chr8:55811618
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360+521G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811618 | ||||||
chr8:55811775
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01978.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2360+678G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811775 | ||||||
chr8:55811851
|
G | A | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2360+754G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811851 | ||||||
chr8:55811905
|
C | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2360+808C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55811905 | ||||||
chr8:55812012
|
C | T | 4 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0280others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360+915C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812012 | ||||||
chr8:55812055
|
T | C | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2360+958T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812055 | ||||||
chr8:55812066
|
A | G | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2360+969A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812066 | ||||||
chr8:55812330
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2361-710C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812330 | ||||||
chr8:55812392
|
G | A | 1 | a0001c0001t0017g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2361-648G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812392 | ||||||
chr8:55812441
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2361-599T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812441 | ||||||
chr8:55812495
|
C | CA | 66 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0020others(63): Show | 77 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2361-525dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | |||||
chr8:55812495
|
C | CAA | 85 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0021others(82): Show | 94 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2361-526_2361-525d others(4): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | |||||
chr8:55812495
|
C | CAAA | 8 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168others(5): Show | 8 | HG00597.hp2 HG04184.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.2361-527_2361-525d others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | |||||
chr8:55812495
|
CA | C | 19 | a0001c0001t0001g0057a0001c0001t0001g0274a0001c0001t0002g0082others(16): Show | 19 | HG00639.hp2 HG00741.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.2361-525delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 55812495 | |||||
chr8:55812640
|
C | T | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2361-400C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812640 | ||||||
chr8:55812765
|
C | T | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2361-275C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812765 | ||||||
chr8:55812827
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0213others(5): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2361-213C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812827 | ||||||
chr8:55812876
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0118 | 2 | HG02135.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2361-164A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55812876 | ||||||
chr8:55813011
|
T | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2361-29T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 11/12 | chr8 | 55813011 | ||||||
chr8:55813146
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2439+28A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813146 | ||||||
chr8:55813159
|
A | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+41A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813159 | ||||||
chr8:55813160
|
C | A | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+42C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813160 | ||||||
chr8:55813192
|
A | T | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+74A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813192 | ||||||
chr8:55813245
|
A | C | 1 | a0001c0020t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2439+127A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813245 | ||||||
chr8:55813302
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2439+184A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813302 | ||||||
chr8:55813354
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2439+236C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813354 | ||||||
chr8:55813424
|
T | G | 6 | a0001c0001t0001g0199a0001c0001t0008g0202a0001c0001t0008g0205others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2439+306T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813424 | ||||||
chr8:55813543
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+425A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813543 | ||||||
chr8:55813708
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2439+590C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813708 | ||||||
chr8:55813718
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.2439+600A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55813718 | ||||||
chr8:55814115
|
T | G | 3 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0310 | 3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2439+997T>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814115 | ||||||
chr8:55814176
|
A | G | 1 | a0002c0002t0003g0306 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2439+1058A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814176 | ||||||
chr8:55814208
|
T | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2439+1090T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814208 | ||||||
chr8:55814240
|
G | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+1122G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814240 | ||||||
chr8:55814316
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2439+1198G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814316 | ||||||
chr8:55814436
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2439+1318T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814436 | ||||||
chr8:55814506
|
T | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2439+1388T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814506 | ||||||
chr8:55814525
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2439+1407C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814525 | ||||||
chr8:55814531
|
T | C | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+1413T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814531 | ||||||
chr8:55814581
|
TG | T | 7 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(4): Show | 7 | HG00597.hp2 NA18943.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.2439+1466delG | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814581 | |||||
chr8:55814601
|
A | G | 1 | a0017c0019t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2439+1483A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814601 | ||||||
chr8:55814650
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2439+1532G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814650 | ||||||
chr8:55814659
|
T | TA | 6 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0274others(3): Show | 7 | HG02717.hp2 NA18950.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.2439+1557dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814659 | |||||
chr8:55814660
|
A | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02280.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+1542A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814660 | ||||||
chr8:55814672
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0119 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2439+1555_2439+155 others(14): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814672 | |||||
chr8:55814672
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2439+1555_2439+155 others(16): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814672 | |||||
chr8:55814672
|
A | ATATATAT | 3 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2439+1554_2439+155 others(11): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814672 | ||||||
chr8:55814672
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2439+1554_2439+155 others(17): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814672 | ||||||
chr8:55814673
|
AAATATAT others(4): Show |
A | 1 | a0003c0003t0005g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2439+1557_2439+156 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814673 | |||||
chr8:55814674
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0001g0126 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2439+1557_2439+155 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | |||||
chr8:55814674
|
A | AAATATAT others(4): Show |
3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | NA18989.hp1 NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2439+1557_2439+155 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | |||||
chr8:55814674
|
A | AAT | 8 | a0001c0001t0001g0219a0001c0001t0006g0194a0001c0001t0007g0040others(5): Show | 9 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1579_2439+158 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | |||||
chr8:55814674
|
A | AATAT | 9 | a0001c0001t0001g0256a0001c0001t0002g0061a0001c0001t0002g0063others(6): Show | 9 | HG02071.hp1 HG02523.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1577_2439+158 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814674 | |||||
chr8:55814674
|
A | ATAT | 20 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0113others(17): Show | 21 | HG00438.hp2 HG01123.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | ||||||
chr8:55814674
|
A | ATATAT | 9 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0131others(6): Show | 9 | HG01109.hp1 HG02109.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(9): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | ||||||
chr8:55814674
|
A | ATATATAT others(2): Show |
4 | a0003c0003t0005g0317a0003c0003t0005g0318a0008c0011t0001g0112others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(13): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | ||||||
chr8:55814674
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0109 | 4 | HG00673.hp2 HG02135.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+1556_2439+155 others(15): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | ||||||
chr8:55814674
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0118 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2439+1556_2439+155 others(17): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | ||||||
chr8:55814674
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2439+1556_2439+155 others(19): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | ||||||
chr8:55814674
|
A | T | 21 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0052others(18): Show | 21 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.2439+1556A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814674 | ||||||
chr8:55814675
|
AT | A | 31 | a0001c0001t0001g0151a0001c0001t0001g0169a0001c0001t0001g0203others(28): Show | 34 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.2439+1558delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814675 | ||||||
chr8:55814676
|
T | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 103 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.2439+1558T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814676 | ||||||
chr8:55814678
|
T | A | 2 | a0001c0001t0001g0260a0002c0002t0003g0303 | 2 | HG02165.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.2439+1560T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814678 | ||||||
chr8:55814730
|
A | G | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+1612A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814730 | ||||||
chr8:55814733
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+1615G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814733 | ||||||
chr8:55814740
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0130others(10): Show | 14 | HG02129.hp1 NA18945.hp2 NA18957.hp1 others(11): Show |
intron_variant | MODIFIER | c.2439+1622C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814740 | ||||||
chr8:55814833
|
C | CT | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+1716dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814833 | |||||
chr8:55814834
|
T | TA | 35 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(32): Show | 38 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.2439+1727dupA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55814834 | |||||
chr8:55814843
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2439+1725A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814843 | ||||||
chr8:55814919
|
T | C | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+1801T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814919 | ||||||
chr8:55814924
|
T | C | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+1806T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814924 | ||||||
chr8:55814960
|
A | G | 1 | a0002c0029t0013g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2439+1842A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55814960 | ||||||
chr8:55815015
|
G | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(34): Show | 41 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(38): Show |
intron_variant | MODIFIER | c.2439+1897G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815015 | ||||||
chr8:55815218
|
CT | C | 4 | a0002c0002t0003g0288a0002c0002t0003g0297a0007c0012t0003g0284others(1): Show | 4 | HG00140.hp1 HG02735.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2439+2103delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815218 | |||||
chr8:55815420
|
G | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(265): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2439+2302G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815420 | ||||||
chr8:55815551
|
C | T | 1 | a0001c0001t0018g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2439+2433C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815551 | ||||||
chr8:55815640
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2439+2522A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815640 | ||||||
chr8:55815843
|
C | A | 1 | a0001c0017t0001g0230 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2439+2725C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815843 | ||||||
chr8:55815918
|
T | TTTTA | 6 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0002g0012others(3): Show | 8 | HG02809.hp2 NA18943.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+2828_2439+283 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815918 | |||||
chr8:55815918
|
TTTTATTT others(1): Show |
T | 35 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(32): Show | 38 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.2439+2824_2439+283 others(12): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815918 | |||||
chr8:55815926
|
A | ATTTATTT others(1981): Show |
1 | a0002c0002t0003g0290 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2439+2823_2439+282 others(1992): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815926 | |||||
chr8:55815930
|
ATTTATTT others(10): Show |
A | 8 | a0001c0001t0002g0104a0003c0003t0005g0312a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+2830_2439+284 others(21): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55815930 | |||||
chr8:55815938
|
A | T | 1 | a0001c0001t0006g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2439+2820A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815938 | ||||||
chr8:55815984
|
G | A | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+2866G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55815984 | ||||||
chr8:55816126
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2439+3008A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816126 | ||||||
chr8:55816187
|
C | T | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3069C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816187 | ||||||
chr8:55816188
|
A | G | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3070A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816188 | ||||||
chr8:55816448
|
C | T | 5 | a0004c0004t0001g0320a0004c0004t0001g0321a0004c0004t0001g0323others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2439+3330C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816448 | ||||||
chr8:55816449
|
T | C | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3331T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816449 | ||||||
chr8:55816656
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2439+3538T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816656 | ||||||
chr8:55816735
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2439+3617G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816735 | ||||||
chr8:55816796
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2439+3678T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816796 | ||||||
chr8:55816860
|
A | AT | 4 | a0001c0001t0001g0048a0001c0001t0001g0055a0001c0001t0001g0167others(1): Show | 4 | HG02080.hp1 HG02109.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439+3745dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55816860 | |||||
chr8:55816864
|
A | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(262): Show | 298 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.2439+3746A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816864 | ||||||
chr8:55816865
|
T | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(248): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.2439+3747T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816865 | ||||||
chr8:55816866
|
T | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0001g0146 | 3 | HG02970.hp1 NA18957.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2439+3748T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816866 | ||||||
chr8:55816867
|
T | A | 1 | a0019c0023t0001g0322 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2439+3749T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816867 | ||||||
chr8:55816870
|
T | A | 47 | a0001c0001t0001g0271a0002c0002t0003g0029a0002c0002t0003g0034others(44): Show | 50 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.2439+3752T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55816870 | ||||||
chr8:55817009
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2439+3891C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817009 | ||||||
chr8:55817049
|
G | T | 10 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(7): Show | 13 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2439+3931G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817049 | ||||||
chr8:55817067
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2439+3949G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817067 | ||||||
chr8:55817109
|
C | T | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+3991C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817109 | ||||||
chr8:55817151
|
C | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+4033C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817151 | ||||||
chr8:55817201
|
A | G | 12 | a0001c0001t0004g0002a0001c0001t0004g0005a0001c0001t0004g0011others(9): Show | 18 | HG00323.hp1 HG00741.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2439+4083A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817201 | ||||||
chr8:55817226
|
G | A | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+4108G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817226 | ||||||
chr8:55817314
|
C | T | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2439+4196C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817314 | ||||||
chr8:55817368
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2439+4250A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817368 | ||||||
chr8:55817518
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2439+4400A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817518 | ||||||
chr8:55817635
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0172 | 3 | NA18971.hp2 NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2439+4517A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817635 | ||||||
chr8:55817688
|
C | T | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2439+4570C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55817688 | ||||||
chr8:55818066
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2439+4948T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818066 | ||||||
chr8:55818093
|
A | G | 31 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(28): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2439+4975A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818093 | ||||||
chr8:55818199
|
A | AT | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+5091dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55818199 | |||||
chr8:55818243
|
T | A | 1 | a0001c0001t0001g0201 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2439+5125T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818243 | ||||||
chr8:55818289
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2439+5171G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818289 | ||||||
chr8:55818455
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2439+5337G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818455 | ||||||
chr8:55818531
|
G | C | 1 | a0002c0029t0013g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2439+5413G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818531 | ||||||
chr8:55818535
|
C | T | 1 | a0003c0003t0005g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2439+5417C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818535 | ||||||
chr8:55818576
|
C | A | 1 | a0018c0018t0001g0325 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2439+5458C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818576 | ||||||
chr8:55818589
|
G | C | 1 | a0001c0001t0002g0127 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2439+5471G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818589 | ||||||
chr8:55818705
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2439+5587A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818705 | ||||||
chr8:55818852
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440-5729G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55818852 | ||||||
chr8:55819033
|
C | T | 1 | a0005c0005t0009g0280 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2440-5548C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819033 | ||||||
chr8:55819171
|
A | G | 8 | a0002c0002t0003g0034a0002c0002t0003g0281a0002c0002t0003g0286others(5): Show | 10 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2440-5410A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819171 | ||||||
chr8:55819288
|
A | AT | 7 | a0001c0001t0002g0100a0001c0001t0002g0104a0001c0001t0002g0105others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2440-5268dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | |||||
chr8:55819288
|
AT | A | 44 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0049others(41): Show | 50 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2440-5268delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | |||||
chr8:55819288
|
ATT | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(151): Show | 173 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.2440-5269_2440-526 others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | |||||
chr8:55819288
|
ATTT | A | 6 | a0001c0001t0001g0184a0001c0001t0006g0152a0002c0002t0003g0299others(3): Show | 6 | HG02145.hp1 HG02965.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.2440-5270_2440-526 others(7): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | |||||
chr8:55819288
|
ATTTT | A | 26 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(23): Show | 29 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2440-5271_2440-526 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | |||||
chr8:55819288
|
ATTTTTTT others(6): Show |
A | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(32): Show | 39 | HG00438.hp2 HG00673.hp2 HG02129.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-5280_2440-526 others(17): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55819288 | |||||
chr8:55819401
|
A | G | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440-5180A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819401 | ||||||
chr8:55819526
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0075a0001c0001t0002g0094 | 4 | NA18943.hp2 NA18973.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440-5055G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819526 | ||||||
chr8:55819553
|
C | A | 1 | a0005c0005t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2440-5028C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819553 | ||||||
chr8:55819618
|
CCTGCCAC others(3): Show |
C | 1 | a0015c0022t0002g0051 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2440-4962_2440-495 others(14): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819618 | ||||||
chr8:55819656
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2440-4925A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55819656 | ||||||
chr8:55820057
|
G | C | 1 | a0001c0001t0002g0066 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2440-4524G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820057 | ||||||
chr8:55820069
|
T | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2440-4512T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820069 | ||||||
chr8:55820104
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2440-4477C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820104 | ||||||
chr8:55820162
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2440-4419A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820162 | ||||||
chr8:55820190
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-4391G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820190 | ||||||
chr8:55820312
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2440-4269C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820312 | ||||||
chr8:55820531
|
C | T | 1 | a0001c0020t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2440-4050C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820531 | ||||||
chr8:55820898
|
G | A | 1 | a0001c0001t0002g0129 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2440-3683G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820898 | ||||||
chr8:55820976
|
A | G | 30 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(27): Show | 33 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.2440-3605A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55820976 | ||||||
chr8:55821150
|
A | T | 3 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0002g0091 | 3 | HG02071.hp2 HG02132.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2440-3431A>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821150 | ||||||
chr8:55821268
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2440-3313G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821268 | ||||||
chr8:55821296
|
T | TGGAGGTG others(660): Show |
1 | a0001c0001t0002g0061 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2440-3268_2440-326 others(671): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55821296 | |||||
chr8:55821399
|
G | C | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2440-3182G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821399 | ||||||
chr8:55821399
|
G | T | 1 | a0002c0002t0003g0324 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2440-3182G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821399 | ||||||
chr8:55821502
|
G | T | 1 | a0015c0022t0002g0051 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2440-3079G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821502 | ||||||
chr8:55821544
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2440-3037G>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821544 | ||||||
chr8:55821623
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2440-2958C>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821623 | ||||||
chr8:55821642
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2440-2939G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821642 | ||||||
chr8:55821679
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2902C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821679 | ||||||
chr8:55821698
|
C | T | 45 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(42): Show | 48 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2440-2883C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821698 | ||||||
chr8:55821700
|
T | C | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2440-2881T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821700 | ||||||
chr8:55821861
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2440-2720C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821861 | ||||||
chr8:55821911
|
CTTTA | C | 6 | a0001c0001t0001g0113a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 7 | HG00438.hp2 HG02698.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2440-2666_2440-266 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55821911 | |||||
chr8:55821950
|
T | C | 1 | a0001c0001t0002g0129 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2440-2631T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55821950 | ||||||
chr8:55821976
|
GAGAT | G | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-2601_2440-259 others(8): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55821976 | |||||
chr8:55822076
|
C | A | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-2505C>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822076 | ||||||
chr8:55822076
|
C | CT | 9 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(6): Show | 9 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2440-2494dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822076 | |||||
chr8:55822076
|
CT | C | 6 | a0001c0001t0001g0151a0004c0004t0001g0320a0004c0004t0001g0321others(3): Show | 7 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2440-2494delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822076 | |||||
chr8:55822080
|
T | C | 3 | a0001c0001t0001g0031a0014c0015t0002g0311a0018c0018t0001g0325 | 3 | HG02258.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2440-2501T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822080 | ||||||
chr8:55822091
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2440-2490G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822091 | ||||||
chr8:55822132
|
C | T | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2440-2449C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822132 | ||||||
chr8:55822156
|
G | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02280.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-2425G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822156 | ||||||
chr8:55822260
|
C | T | 1 | a0005c0005t0002g0309 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2440-2321C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822260 | ||||||
chr8:55822284
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2440-2297A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822284 | ||||||
chr8:55822366
|
G | A | 28 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(25): Show | 31 | HG00140.hp1 HG01109.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.2440-2215G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822366 | ||||||
chr8:55822454
|
T | C | 1 | a0001c0014t0001g0154 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2440-2127T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822454 | ||||||
chr8:55822476
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2440-2105A>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822476 | ||||||
chr8:55822530
|
T | C | 1 | a0014c0015t0002g0311 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2440-2051T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822530 | ||||||
chr8:55822549
|
C | CT | 8 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0213others(5): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2440-2020dupT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822549 | |||||
chr8:55822549
|
CT | C | 15 | a0001c0001t0001g0113a0002c0002t0003g0288a0002c0002t0003g0297others(12): Show | 15 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2440-2020delT | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55822549 | |||||
chr8:55822559
|
T | C | 1 | a0002c0002t0003g0034 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2440-2022T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822559 | ||||||
chr8:55822559
|
T | TC | 9 | a0002c0002t0003g0029a0002c0002t0003g0281a0002c0002t0003g0285others(6): Show | 12 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2440-2022_2440-202 others(5): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822559 | ||||||
chr8:55822560
|
T | C | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-2021T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822560 | ||||||
chr8:55822561
|
T | C | 74 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(71): Show | 81 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2440-2020T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822561 | ||||||
chr8:55822653
|
T | C | 1 | a0002c0002t0003g0294 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2440-1928T>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822653 | ||||||
chr8:55822717
|
G | A | 8 | a0003c0003t0005g0312a0003c0003t0005g0313a0003c0003t0005g0314others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440-1864G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822717 | ||||||
chr8:55822807
|
T | A | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2440-1774T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822807 | ||||||
chr8:55822908
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2440-1673C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822908 | ||||||
chr8:55822961
|
A | G | 44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 48 | HG00438.hp2 HG00673.hp2 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.2440-1620A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822961 | ||||||
chr8:55822975
|
T | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0133a0001c0001t0001g0134 | 4 | NA18957.hp1 NA18994.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1606T>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55822975 | ||||||
chr8:55823121
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2440-1460C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823121 | ||||||
chr8:55823178
|
A | G | 36 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(33): Show | 39 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2440-1403A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823178 | ||||||
chr8:55823267
|
A | G | 44 | a0002c0002t0003g0029a0002c0002t0003g0034a0002c0002t0003g0281others(41): Show | 47 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.2440-1314A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823267 | ||||||
chr8:55823292
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2440-1289C>T | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55823292 | ||||||
chr8:55823950
|
TA | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(263): Show | 299 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.2440-623delA | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55823950 | |||||
chr8:55824071
|
G | A | 1 | a0002c0029t0013g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2440-510G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824071 | ||||||
chr8:55824095
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(220): Show | 253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.2440-486G>A | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824095 | ||||||
chr8:55824210
|
CAGTG | C | 4 | a0005c0005t0009g0278a0005c0005t0009g0279a0005c0005t0009g0280others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-368_2440-365d others(6): Show |
TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 55824210 | |||||
chr8:55824417
|
A | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0028others(6): Show | 15 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.2440-164A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824417 | ||||||
chr8:55824422
|
A | G | 6 | a0001c0001t0001g0033a0001c0001t0001g0114a0001c0001t0001g0115others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440-159A>G | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824422 | ||||||
chr8:55824487
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG02129.hp1 NA18986.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-94G>C | TGS1 | ENSG00000137574.11 | transcript | ENST00000260129.6 | protein_coding | 12/12 | chr8 | 55824487 |