geneid | 29968 |
---|---|
ensemblid | ENSG00000135069.14 |
hgncid | 19129 |
symbol | PSAT1 |
name | phosphoserine aminotransferase 1 |
refseq_nuc | NM_058179.4 |
refseq_prot | NP_478059.1 |
ensembl_nuc | ENST00000376588.4 |
ensembl_prot | ENSP00000365773.3 |
mane_status | MANE Select |
chr | chr9 |
start | 78297125 |
end | 78330093 |
strand | + |
ver | v1.2 |
region | chr9:78297125-78330093 |
region5000 | chr9:78292125-78335093 |
regionname0 | PSAT1_chr9_78297125_78330093 |
regionname5000 | PSAT1_chr9_78292125_78335093 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 370 | 412 | 95 | 74 | 181 | 16 | 44 | 137 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0002 | 0/0 | 370 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0003 | 0/0 | 370 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0004 | 0/0 | 370 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0005 | 0/0 | 370 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1113 | 244 | 43 | 39 | 129 | 7 | 25 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0002 | 0/1 | 1113 | 164 | 51 | 34 | 51 | 9 | 18 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0003 | 0/0 | 1113 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0004 | 0/0 | 1113 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0005 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0006 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0007 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0008 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
c0009 | 0/0 | 1113 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1094 | 261 | 52 | 46 | 124 | 13 | 25 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0002 | 1/0 | 1094 | 105 | 7 | 16 | 58 | 3 | 20 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0003 | 0/0 | 1094 | 26 | 16 | 9 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0004 | 0/0 | 1094 | 12 | 11 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0005 | 0/0 | 1094 | 4 | 3 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0006 | 0/0 | 1094 | 3 | 2 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0007 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0008 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0009 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0010 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
t0011 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 4 | 6 | 0 | 2 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0008 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1113 | 244 | 43 | 39 | 129 | 7 | 25 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002 | 0/1 | 1113 | 164 | 51 | 34 | 51 | 9 | 18 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0003 | 0/0 | 1113 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0005 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0009 | 0/0 | 1113 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0002c0004 | 0/0 | 1113 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0003c0007 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0004c0006 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0005c0008 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2206 | 134 | 21 | 18 | 84 | 4 | 7 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0001t0002 | 1/0 | 2206 | 81 | 4 | 11 | 45 | 3 | 17 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0001t0003 | 0/0 | 2206 | 16 | 7 | 8 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0001t0004 | 0/0 | 2206 | 9 | 8 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0001t0005 | 0/0 | 2206 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0001t0009 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0001t0011 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0001 | 0/1 | 2206 | 123 | 31 | 28 | 39 | 9 | 15 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0002 | 0/0 | 2206 | 23 | 3 | 5 | 12 | 0 | 3 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0003 | 0/0 | 2206 | 9 | 8 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0004 | 0/0 | 2206 | 3 | 3 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0005 | 0/0 | 2206 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0006 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0007 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0008 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0002t0010 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0003t0006 | 0/0 | 2206 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0005t0001 | 0/0 | 2206 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0001c0009t0002 | 0/0 | 2206 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0002c0004t0001 | 0/0 | 2206 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0003c0007t0001 | 0/0 | 2206 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0004c0006t0001 | 0/0 | 2206 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
a0005c0008t0003 | 0/0 | 2206 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | copy fasta | chr9 | 78292125 | 78335093 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0110 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0004g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0009g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0001 | 0/0 | 12 | 0 | 4 | 6 | 0 | 2 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0006g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0002t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0003t0006g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0001c0009t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0002c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0003c0007t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0004c0006t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
a0005c0008t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0233 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0115 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0178 | EUR | GBR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0027 | EUR | FIN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0318 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0332 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01081 | hp2 | a0001 | c0003 | t0006 | g0009 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0281 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0239 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0244 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0348 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0321 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0363 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0065 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0296 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0230 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01891 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0088 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0289 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02145 | hp2 | a0001 | c0002 | t0008 | g0021 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CDX | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PEL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0246 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | KHV | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0354 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0334 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02698 | hp2 | a0001 | c0005 | t0001 | g0312 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0358 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0089 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02809 | hp2 | a0001 | c0002 | t0010 | g0043 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0327 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0276 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0245 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0141 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0347 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0355 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0360 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03130 | hp1 | a0001 | c0003 | t0006 | g0009 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0273 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | ESN | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0359 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03225 | hp2 | a0001 | c0002 | t0004 | g0190 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0044 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0189 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03579 | hp1 | a0005 | c0008 | t0003 | g0142 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03654 | hp1 | a0004 | c0006 | t0001 | g0326 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0346 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03704 | hp2 | a0003 | c0007 | t0001 | g0177 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0128 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0335 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0129 | SAS | BEB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18995 | hp1 | a0002 | c0004 | t0001 | g0175 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0357 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19084 | hp1 | a0001 | c0009 | t0002 | g0116 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19240 | hp1 | a0001 | c0002 | t0005 | g0138 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0228 | AFR | YRI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ASW | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ASW | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0258 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0130 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0336 | EUR | TSI | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0226 | SAS | GIH | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0313 | SAS | GIH | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0338 | AMR | CLM | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02109 | hp1 | a0001 | c0002 | t0004 | g0322 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02486 | hp1 | a0001 | c0002 | t0007 | g0259 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0330 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG03471 | hp2 | a0001 | c0002 | t0006 | g0356 | AFR | MSL | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0301 | AFR | USA | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0310 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | LWK | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0242 | REF | REF | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0110 | REF | REF | PSAT1_chr9_78292125_78335093 | PSAT1 | chr9 | 78292125 | 78335093 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:78300603
|
T | G | 1 | a0002 | 1 | NA18995.hp1 | missense_variant&splice_region_variant | MODERATE | c.62T>G | p.Val21Gly | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/9 | 148/2206 | 62/1113 | 21/370 | chr9 | 78300603 | ||
chr9:78304910
|
A | G | 1 | a0005 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.367A>G | p.Ile123Val | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/9 | 453/2206 | 367/1113 | 123/370 | chr9 | 78304910 | ||
chr9:78308568
|
C | T | 1 | a0003 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.725C>T | p.Thr242Met | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/9 | 811/2206 | 725/1113 | 242/370 | chr9 | 78308568 | ||
chr9:78317684
|
T | C | 1 | a0004 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.749T>C | p.Val250Ala | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/9 | 835/2206 | 749/1113 | 250/370 | chr9 | 78317684 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:78304840
|
T | G | 5 | a0001c0002a0001c0005a0003c0007others(2): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
synonymous_variant | LOW | c.297T>G | p.Ala99Ala | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/9 | 383/2206 | 297/1113 | 99/370 | chr9 | 78304840 | ||
chr9:78304891
|
G | A | 1 | a0001c0005 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.348G>A | p.Lys116Lys | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/9 | 434/2206 | 348/1113 | 116/370 | chr9 | 78304891 | ||
chr9:78317730
|
G | A | 1 | a0001c0003 | 2 | HG01081.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.795G>A | p.Ala265Ala | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/9 | 881/2206 | 795/1113 | 265/370 | chr9 | 78317730 | ||
chr9:78329032
|
C | T | 1 | a0001c0009 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.1059C>T | p.Asp353Asp | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 1145/2206 | 1059/1113 | 353/370 | chr9 | 78329032 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:78297173
|
G | A | 1 | a0001c0002t0007 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/9 | 38 | chr9 | 78297173 | |||||
chr9:78297199
|
G | C | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
5_prime_UTR_variant | MODIFIER | c.-12G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/9 | 12 | chr9 | 78297199 | |||||
chr9:78329125
|
A | G | 1 | a0001c0001t0011 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 39 | chr9 | 78329125 | |||||
chr9:78329337
|
C | T | 1 | a0001c0002t0010 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 251 | chr9 | 78329337 | |||||
chr9:78329338
|
G | C | 4 | a0001c0001t0004a0001c0002t0004a0001c0002t0006others(1): Show | 15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*252G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 252 | chr9 | 78329338 | |||||
chr9:78329508
|
C | T | 7 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(4): Show | 32 | HG00738.hp2 HG01081.hp1 HG01346.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 422 | chr9 | 78329508 | |||||
chr9:78329678
|
A | C | 4 | a0001c0001t0004a0001c0002t0004a0001c0002t0006others(1): Show | 15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*592A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 592 | chr9 | 78329678 | |||||
chr9:78329750
|
A | G | 1 | a0001c0002t0008 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 664 | chr9 | 78329750 | |||||
chr9:78329888
|
A | T | 1 | a0001c0001t0009 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 9/9 | 802 | chr9 | 78329888 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:78297385
|
A | G | 1 | a0001c0002t0001g0363 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.60+115A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297385 | ||||||
chr9:78297481
|
C | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.60+211C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297481 | ||||||
chr9:78297530
|
C | T | 2 | a0001c0001t0001g0361a0001c0001t0001g0362 | 2 | NA18944.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.60+260C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297530 | ||||||
chr9:78297539
|
G | T | 1 | a0001c0002t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.60+269G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297539 | ||||||
chr9:78297651
|
C | G | 3 | a0001c0002t0001g0358a0001c0002t0001g0359a0001c0002t0001g0360 | 3 | HG02717.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.60+381C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297651 | ||||||
chr9:78297680
|
C | T | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+410C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297680 | ||||||
chr9:78297819
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+549C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297819 | ||||||
chr9:78297870
|
G | A | 2 | a0001c0002t0001g0140a0001c0002t0003g0141 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.60+600G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297870 | ||||||
chr9:78297907
|
G | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(79): Show | 90 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.60+637G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297907 | ||||||
chr9:78297913
|
C | T | 2 | a0001c0002t0001g0355a0001c0002t0003g0354 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.60+643C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297913 | ||||||
chr9:78297914
|
C | G | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+644C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78297914 | ||||||
chr9:78298118
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.60+848G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298118 | ||||||
chr9:78298154
|
G | C | 90 | a0001c0001t0001g0024a0001c0001t0001g0145a0001c0001t0001g0197others(87): Show | 105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+884G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298154 | ||||||
chr9:78298170
|
C | G | 3 | a0001c0002t0001g0030a0001c0002t0001g0136a0001c0002t0001g0137 | 4 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+900C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298170 | ||||||
chr9:78298405
|
C | T | 10 | a0001c0002t0001g0030a0001c0002t0001g0136a0001c0002t0001g0137others(7): Show | 11 | HG02257.hp1 HG02258.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+1135C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298405 | ||||||
chr9:78298653
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0350a0001c0001t0001g0351others(2): Show | 6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+1383A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298653 | ||||||
chr9:78298778
|
T | G | 1 | a0001c0001t0004g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.60+1508T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78298778 | ||||||
chr9:78299013
|
G | A | 30 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(27): Show | 36 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.61-1589G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299013 | ||||||
chr9:78299121
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.61-1481T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299121 | ||||||
chr9:78299144
|
C | CA | 26 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0001t0001g0325others(23): Show | 28 | HG00642.hp1 HG01106.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.61-1430dupA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0030 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.61-1455_61-1430dup others(26): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
C | CAAAAAAA others(23): Show |
1 | a0001c0002t0001g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.61-1430_61-1429ins others(30): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
C | CAAAAAAA others(24): Show |
1 | a0001c0002t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-1430_61-1429ins others(31): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
CA | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0035others(2): Show | 6 | HG02717.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-1430delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
CAA | C | 13 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(10): Show | 14 | HG00544.hp1 HG01978.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-1431_61-1430del others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
CAAA | C | 78 | a0001c0001t0001g0031a0001c0001t0001g0207a0001c0001t0001g0211others(75): Show | 96 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.61-1432_61-1430del others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
CAAAAAAA others(2): Show |
C | 42 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0153others(39): Show | 49 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.61-1438_61-1430del others(9): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
CAAAAAAA others(3): Show |
C | 64 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0029others(61): Show | 71 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.61-1439_61-1430del others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299144
|
CAAAAAAA others(4): Show |
C | 43 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(40): Show | 51 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.61-1440_61-1430del others(11): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299144 | |||||
chr9:78299158
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61-1444A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299158 | ||||||
chr9:78299164
|
A | G | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61-1438A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299164 | ||||||
chr9:78299180
|
T | C | 1 | a0001c0002t0001g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61-1422T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299180 | ||||||
chr9:78299211
|
G | GA | 7 | a0001c0001t0001g0262a0001c0001t0003g0310a0001c0002t0001g0281others(4): Show | 7 | HG01192.hp1 HG01433.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-1380dupA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | |||||
chr9:78299211
|
G | GAA | 138 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0025others(135): Show | 167 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.61-1381_61-1380dup others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | |||||
chr9:78299211
|
G | GAAA | 69 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0029others(66): Show | 77 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.61-1382_61-1380dup others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | |||||
chr9:78299211
|
G | GAAAA | 40 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(37): Show | 47 | HG00408.hp1 HG00544.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.61-1383_61-1380dup others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299211 | |||||
chr9:78299269
|
CTG | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1331_61-1330del others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299269 | |||||
chr9:78299271
|
G | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(246): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.61-1331G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299271 | ||||||
chr9:78299273
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1329T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299273 | ||||||
chr9:78299369
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61-1233C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299369 | ||||||
chr9:78299465
|
A | C | 1 | a0001c0002t0001g0321 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.61-1137A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299465 | ||||||
chr9:78299496
|
C | CT | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(250): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.61-1098dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299496 | |||||
chr9:78299514
|
C | CT | 11 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0349others(8): Show | 11 | HG01243.hp1 HG01346.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1070dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | |||||
chr9:78299514
|
C | CTT | 104 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0025others(101): Show | 121 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.61-1071_61-1070dup others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | |||||
chr9:78299514
|
C | CTTT | 136 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(133): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.61-1072_61-1070dup others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | |||||
chr9:78299514
|
C | CTTTT | 9 | a0001c0001t0001g0257a0001c0001t0001g0283a0001c0002t0001g0136others(6): Show | 9 | HG00408.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.61-1073_61-1070dup others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299514 | |||||
chr9:78299554
|
C | T | 4 | a0001c0001t0001g0308a0001c0002t0001g0140a0001c0002t0003g0141others(1): Show | 4 | HG02976.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1048C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299554 | ||||||
chr9:78299555
|
G | T | 2 | a0001c0002t0002g0039a0001c0002t0002g0040 | 2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.61-1047G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299555 | ||||||
chr9:78299571
|
C | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.61-1031C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299571 | ||||||
chr9:78299581
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.61-1021C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299581 | ||||||
chr9:78299593
|
ACCTCCGC others(25): Show |
A | 5 | a0001c0001t0001g0029a0001c0001t0001g0350a0001c0001t0001g0351others(2): Show | 6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-997_61-966delCG others(30): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 78299593 | |||||
chr9:78299630
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0004g0194a0001c0002t0010g0043 | 3 | HG02809.hp2 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.61-972C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299630 | ||||||
chr9:78299697
|
G | C | 1 | a0001c0001t0004g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.61-905G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299697 | ||||||
chr9:78299702
|
G | A | 1 | a0001c0002t0001g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.61-900G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299702 | ||||||
chr9:78299713
|
A | G | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.61-889A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299713 | ||||||
chr9:78299718
|
G | C | 1 | a0001c0002t0001g0140 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61-884G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78299718 | ||||||
chr9:78300190
|
C | T | 16 | a0001c0001t0002g0063a0001c0001t0004g0147a0001c0001t0005g0064others(13): Show | 19 | HG01081.hp2 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-412C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300190 | ||||||
chr9:78300386
|
A | G | 2 | a0001c0002t0001g0355a0001c0002t0003g0354 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.61-216A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300386 | ||||||
chr9:78300435
|
G | T | 3 | a0001c0002t0001g0030a0001c0002t0001g0136a0001c0002t0001g0137 | 4 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-167G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300435 | ||||||
chr9:78300476
|
G | A | 59 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0029others(56): Show | 66 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-126G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300476 | ||||||
chr9:78300487
|
A | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(250): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.61-115A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300487 | ||||||
chr9:78300494
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.61-108G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300494 | ||||||
chr9:78300564
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.61-38A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300564 | ||||||
chr9:78300580
|
A | G | 1 | a0001c0002t0002g0089 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.61-22A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 1/8 | chr9 | 78300580 | ||||||
chr9:78300710
|
C | CT | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(184): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.121+70dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78300710 | |||||
chr9:78300710
|
C | CTT | 43 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0033others(40): Show | 49 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.121+69_121+70dupTT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78300710 | |||||
chr9:78300710
|
CT | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0001t0002g0090others(15): Show | 21 | HG00642.hp1 HG01070.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+70delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78300710 | |||||
chr9:78300732
|
T | C | 1 | a0001c0001t0002g0075 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.121+70T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300732 | ||||||
chr9:78300762
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0002t0003g0273 | 5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+100C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300762 | ||||||
chr9:78300776
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0350a0001c0001t0001g0351others(2): Show | 6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+114C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300776 | ||||||
chr9:78300777
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 9 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+115G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300777 | ||||||
chr9:78300843
|
G | C | 2 | a0001c0002t0001g0358a0001c0002t0001g0359 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.121+181G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300843 | ||||||
chr9:78300890
|
T | A | 1 | a0001c0002t0001g0320 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.121+228T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78300890 | ||||||
chr9:78301090
|
G | A | 1 | a0001c0002t0001g0328 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.121+428G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301090 | ||||||
chr9:78301278
|
G | A | 84 | a0001c0001t0001g0031a0001c0001t0001g0198a0001c0001t0001g0207others(81): Show | 103 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.121+616G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301278 | ||||||
chr9:78301330
|
A | G | 92 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(89): Show | 112 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.122-624A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301330 | ||||||
chr9:78301367
|
TA | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0002t0003g0273 | 5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-585delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 78301367 | |||||
chr9:78301442
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122-512G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301442 | ||||||
chr9:78301460
|
T | A | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.122-494T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301460 | ||||||
chr9:78301466
|
A | G | 92 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(89): Show | 112 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.122-488A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301466 | ||||||
chr9:78301474
|
C | T | 1 | a0001c0002t0010g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.122-480C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301474 | ||||||
chr9:78301504
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-450C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301504 | ||||||
chr9:78301699
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(239): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.122-255G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301699 | ||||||
chr9:78301885
|
G | A | 2 | a0001c0001t0003g0324a0001c0002t0001g0323 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.122-69G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301885 | ||||||
chr9:78301937
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.122-17T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 2/8 | chr9 | 78301937 | ||||||
chr9:78302063
|
A | G | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+40A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302063 | ||||||
chr9:78302154
|
C | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0029others(56): Show | 66 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.191+131C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302154 | ||||||
chr9:78302180
|
C | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(239): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.191+157C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302180 | ||||||
chr9:78302197
|
C | T | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+174C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302197 | ||||||
chr9:78302442
|
A | G | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+419A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302442 | ||||||
chr9:78302464
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.191+441C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302464 | ||||||
chr9:78302494
|
C | T | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.191+471C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302494 | ||||||
chr9:78302537
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+514G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302537 | ||||||
chr9:78302570
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.191+547C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302570 | ||||||
chr9:78302621
|
C | G | 1 | a0001c0002t0002g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.191+598C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302621 | ||||||
chr9:78302626
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(124): Show | 147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.191+603C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302626 | ||||||
chr9:78302733
|
C | CA | 41 | a0001c0001t0001g0024a0001c0001t0001g0095a0001c0001t0001g0104others(38): Show | 43 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.191+738dupA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | |||||
chr9:78302733
|
C | CAA | 6 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0001t0002g0092others(3): Show | 8 | HG00642.hp1 HG01070.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.191+737_191+738dup others(2): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | |||||
chr9:78302733
|
CA | C | 9 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0188others(6): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.191+738delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | |||||
chr9:78302733
|
CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0157others(7): Show | 10 | HG02055.hp1 HG02074.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.191+731_191+738del others(8): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | |||||
chr9:78302733
|
CAAAAAAA others(2): Show |
C | 201 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(198): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.191+730_191+738del others(9): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | |||||
chr9:78302733
|
CAAAAAAA others(3): Show |
C | 10 | a0001c0001t0002g0068a0001c0001t0002g0071a0001c0001t0003g0156others(7): Show | 10 | HG01168.hp2 HG01975.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.191+729_191+738del others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 78302733 | |||||
chr9:78302788
|
G | C | 6 | a0001c0001t0002g0063a0001c0001t0004g0147a0001c0001t0005g0064others(3): Show | 7 | HG01081.hp2 HG01496.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+765G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302788 | ||||||
chr9:78302810
|
G | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+787G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302810 | ||||||
chr9:78302830
|
C | T | 1 | a0001c0002t0003g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.191+807C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302830 | ||||||
chr9:78302861
|
G | A | 15 | a0001c0001t0002g0063a0001c0001t0004g0147a0001c0001t0005g0064others(12): Show | 18 | HG01081.hp2 HG01243.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.191+838G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302861 | ||||||
chr9:78302877
|
C | T | 1 | a0001c0003t0006g0009 | 2 | HG01081.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.191+854C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302877 | ||||||
chr9:78302997
|
G | A | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.191+974G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78302997 | ||||||
chr9:78303041
|
A | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0025others(52): Show | 68 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.191+1018A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303041 | ||||||
chr9:78303046
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.191+1023T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303046 | ||||||
chr9:78303345
|
A | C | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+1322A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303345 | ||||||
chr9:78303417
|
A | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(220): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.192-1318A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303417 | ||||||
chr9:78303504
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(220): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.192-1231C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303504 | ||||||
chr9:78303548
|
T | G | 242 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(239): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.192-1187T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303548 | ||||||
chr9:78303684
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.192-1051T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303684 | ||||||
chr9:78303693
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.192-1042C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303693 | ||||||
chr9:78303910
|
T | G | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192-825T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303910 | ||||||
chr9:78303921
|
C | G | 15 | a0001c0001t0002g0063a0001c0001t0004g0147a0001c0001t0005g0064others(12): Show | 18 | HG01081.hp2 HG01243.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.192-814C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303921 | ||||||
chr9:78303980
|
T | C | 8 | a0001c0001t0001g0031a0001c0001t0004g0004a0001c0001t0004g0278others(5): Show | 11 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.192-755T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78303980 | ||||||
chr9:78304037
|
T | C | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192-698T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304037 | ||||||
chr9:78304079
|
T | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(279): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.192-656T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304079 | ||||||
chr9:78304268
|
C | T | 1 | a0001c0002t0001g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.192-467C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304268 | ||||||
chr9:78304348
|
G | A | 1 | a0001c0001t0004g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.192-387G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304348 | ||||||
chr9:78304353
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192-382G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304353 | ||||||
chr9:78304547
|
C | G | 1 | a0001c0002t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.192-188C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304547 | ||||||
chr9:78304612
|
G | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0033others(6): Show | 11 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.192-123G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304612 | ||||||
chr9:78304687
|
T | C | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-48T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 3/8 | chr9 | 78304687 | ||||||
chr9:78305039
|
G | GT | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.397+100dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | 78305039 | |||||
chr9:78305137
|
C | T | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.397+197C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305137 | ||||||
chr9:78305217
|
C | T | 2 | a0001c0002t0001g0256a0001c0002t0005g0138 | 2 | NA18961.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.397+277C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305217 | ||||||
chr9:78305269
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.397+329C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305269 | ||||||
chr9:78305272
|
G | A | 1 | a0001c0002t0002g0050 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.397+332G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305272 | ||||||
chr9:78305370
|
C | T | 10 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0139others(7): Show | 12 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.397+430C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305370 | ||||||
chr9:78305413
|
C | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0033others(6): Show | 11 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+473C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305413 | ||||||
chr9:78305526
|
C | G | 2 | a0001c0001t0002g0106a0001c0001t0002g0124 | 2 | HG01109.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.397+586C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305526 | ||||||
chr9:78305573
|
G | C | 9 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0187others(6): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+633G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305573 | ||||||
chr9:78305841
|
C | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.398-473C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305841 | ||||||
chr9:78305869
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.398-445T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305869 | ||||||
chr9:78305991
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.398-323G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78305991 | ||||||
chr9:78306102
|
G | C | 1 | a0001c0002t0001g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.398-212G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306102 | ||||||
chr9:78306105
|
G | A | 35 | a0001c0002t0001g0007a0001c0002t0001g0027a0001c0002t0001g0030others(32): Show | 39 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.398-209G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306105 | ||||||
chr9:78306172
|
T | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(255): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.398-142T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306172 | ||||||
chr9:78306229
|
C | T | 27 | a0001c0002t0001g0007a0001c0002t0001g0027a0001c0002t0001g0030others(24): Show | 31 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.398-85C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 4/8 | chr9 | 78306229 | ||||||
chr9:78306530
|
G | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(255): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.570+44G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306530 | ||||||
chr9:78306565
|
AAGAACCA others(18): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.570+86_570+110delA others(24): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 78306565 | |||||
chr9:78306683
|
C | T | 87 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0016others(84): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.570+197C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306683 | ||||||
chr9:78306816
|
C | T | 87 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0016others(84): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.570+330C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306816 | ||||||
chr9:78306888
|
C | T | 2 | a0001c0002t0001g0240a0001c0002t0001g0241 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.570+402C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306888 | ||||||
chr9:78306921
|
G | C | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+435G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78306921 | ||||||
chr9:78307041
|
A | G | 1 | a0001c0002t0001g0323 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570+555A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307041 | ||||||
chr9:78307208
|
G | A | 1 | a0001c0002t0001g0219 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.570+722G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307208 | ||||||
chr9:78307251
|
A | G | 1 | a0001c0001t0003g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+765A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307251 | ||||||
chr9:78307373
|
G | C | 35 | a0001c0002t0001g0007a0001c0002t0001g0027a0001c0002t0001g0030others(32): Show | 39 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.570+887G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307373 | ||||||
chr9:78307381
|
A | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0242 | 2 | HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.570+895A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307381 | ||||||
chr9:78307401
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.570+915G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307401 | ||||||
chr9:78307478
|
A | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.571-936A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307478 | ||||||
chr9:78307517
|
C | T | 2 | a0001c0002t0001g0238a0001c0002t0001g0239 | 2 | HG00733.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.571-897C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307517 | ||||||
chr9:78307542
|
G | A | 35 | a0001c0002t0001g0007a0001c0002t0001g0027a0001c0002t0001g0030others(32): Show | 39 | HG00323.hp2 HG01074.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.571-872G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307542 | ||||||
chr9:78307621
|
C | A | 1 | a0005c0008t0003g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.571-793C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307621 | ||||||
chr9:78307745
|
T | TAAAAAAT others(322): Show |
1 | a0001c0002t0001g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.571-654_571-653ins others(329): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 78307745 | |||||
chr9:78307745
|
T | TAAAAAAT others(323): Show |
1 | a0001c0002t0006g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.571-654_571-653ins others(330): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 78307745 | |||||
chr9:78307781
|
C | A | 1 | a0001c0001t0004g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-633C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307781 | ||||||
chr9:78307894
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.571-520A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307894 | ||||||
chr9:78307912
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.571-502C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307912 | ||||||
chr9:78307964
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.571-450G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307964 | ||||||
chr9:78307980
|
A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0033others(7): Show | 12 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-434A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78307980 | ||||||
chr9:78308053
|
AT | A | 4 | a0001c0001t0001g0331a0001c0001t0001g0339a0001c0001t0001g0344others(1): Show | 4 | NA18942.hp1 NA19010.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-360delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308053 | ||||||
chr9:78308131
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(104): Show | 120 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.571-283G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308131 | ||||||
chr9:78308207
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.571-207C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308207 | ||||||
chr9:78308210
|
G | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0001t0003g0324 | 5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-204G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308210 | ||||||
chr9:78308249
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 125 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.571-165G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308249 | ||||||
chr9:78308334
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 125 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.571-80C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 5/8 | chr9 | 78308334 | ||||||
chr9:78308644
|
G | A | 1 | a0001c0002t0002g0003 | 4 | NA18943.hp2 NA18952.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+61G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308644 | ||||||
chr9:78308682
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0262a0001c0001t0001g0264others(4): Show | 8 | HG00438.hp2 NA18952.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.740+99G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308682 | ||||||
chr9:78308693
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.740+110C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308693 | ||||||
chr9:78308694
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.740+111A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308694 | ||||||
chr9:78308712
|
T | C | 2 | a0001c0001t0005g0064a0001c0001t0005g0065 | 2 | HG01496.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.740+129T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308712 | ||||||
chr9:78308713
|
T | G | 40 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0001t0003g0324others(37): Show | 46 | HG00323.hp2 HG00642.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.740+130T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308713 | ||||||
chr9:78308759
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.740+176T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308759 | ||||||
chr9:78308791
|
A | G | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.740+208A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308791 | ||||||
chr9:78308816
|
G | A | 3 | a0001c0001t0001g0288a0001c0001t0001g0291a0001c0001t0001g0292 | 3 | NA18950.hp1 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.740+233G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308816 | ||||||
chr9:78308903
|
C | T | 262 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.740+320C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308903 | ||||||
chr9:78308918
|
G | GCACT | 8 | a0001c0002t0001g0140a0001c0002t0001g0355a0001c0002t0001g0358others(5): Show | 8 | HG02572.hp2 HG02717.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.740+337_740+340dup others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78308918 | |||||
chr9:78308967
|
T | C | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.740+384T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78308967 | ||||||
chr9:78309092
|
A | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.740+509A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309092 | ||||||
chr9:78309174
|
C | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0033others(8): Show | 13 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.740+591C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309174 | ||||||
chr9:78309193
|
C | G | 1 | a0001c0002t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.740+610C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309193 | ||||||
chr9:78309203
|
C | G | 2 | a0001c0001t0002g0122a0001c0001t0002g0123 | 2 | NA18970.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.740+620C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309203 | ||||||
chr9:78309232
|
C | G | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+649C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309232 | ||||||
chr9:78309246
|
A | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0001t0003g0324 | 5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.740+663A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309246 | ||||||
chr9:78309305
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.740+722G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309305 | ||||||
chr9:78309335
|
A | G | 1 | a0001c0002t0002g0059 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.740+752A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309335 | ||||||
chr9:78309386
|
C | T | 4 | a0001c0001t0002g0084a0001c0001t0002g0091a0001c0001t0002g0105others(1): Show | 4 | NA18978.hp1 NA18983.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.740+803C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309386 | ||||||
chr9:78309395
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(104): Show | 120 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.740+812G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309395 | ||||||
chr9:78309423
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 166 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.740+840C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309423 | ||||||
chr9:78309451
|
C | T | 1 | a0001c0002t0001g0182 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.740+868C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309451 | ||||||
chr9:78309485
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 168 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.740+902C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309485 | ||||||
chr9:78309507
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 168 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.740+924T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309507 | ||||||
chr9:78309517
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 168 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.740+934T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309517 | ||||||
chr9:78309620
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 168 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.740+1037T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309620 | ||||||
chr9:78309726
|
C | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 168 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.740+1143C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309726 | ||||||
chr9:78309737
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(106): Show | 122 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.740+1154G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309737 | ||||||
chr9:78309765
|
G | A | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+1182G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309765 | ||||||
chr9:78309933
|
C | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(143): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+1350C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78309933 | ||||||
chr9:78310109
|
G | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | NA18941.hp2 NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.740+1526G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310109 | ||||||
chr9:78310159
|
G | A | 2 | a0001c0002t0003g0245a0001c0002t0003g0246 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.740+1576G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310159 | ||||||
chr9:78310162
|
A | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(143): Show | 163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.740+1579A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310162 | ||||||
chr9:78310197
|
T | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+1614T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310197 | ||||||
chr9:78310303
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+1720T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310303 | ||||||
chr9:78310382
|
G | T | 1 | a0005c0008t0003g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.740+1799G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310382 | ||||||
chr9:78310484
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740+1901C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310484 | ||||||
chr9:78310616
|
A | ATTT | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(99): Show | 115 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.740+2045_740+2047d others(5): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78310616 | |||||
chr9:78310616
|
A | ATTTT | 42 | a0001c0001t0001g0048a0001c0001t0001g0184a0001c0001t0001g0299others(39): Show | 46 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.740+2044_740+2047d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78310616 | |||||
chr9:78310641
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2058T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310641 | ||||||
chr9:78310643
|
C | T | 2 | a0001c0002t0001g0146a0001c0002t0001g0337 | 2 | NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.740+2060C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310643 | ||||||
chr9:78310703
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2120C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310703 | ||||||
chr9:78310734
|
A | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2151A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310734 | ||||||
chr9:78310787
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(107): Show | 123 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.740+2204T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310787 | ||||||
chr9:78310844
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0025others(49): Show | 62 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.740+2261G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310844 | ||||||
chr9:78310883
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2300C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310883 | ||||||
chr9:78310920
|
G | A | 1 | a0001c0002t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.740+2337G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310920 | ||||||
chr9:78310942
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2359G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310942 | ||||||
chr9:78310961
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2378C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310961 | ||||||
chr9:78310966
|
C | T | 10 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0139others(7): Show | 12 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.740+2383C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78310966 | ||||||
chr9:78311219
|
A | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2636A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311219 | ||||||
chr9:78311257
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+2674T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311257 | ||||||
chr9:78311284
|
C | T | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.740+2701C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311284 | ||||||
chr9:78311470
|
T | C | 1 | a0005c0008t0003g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.740+2887T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311470 | ||||||
chr9:78311535
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.740+2952T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311535 | ||||||
chr9:78311571
|
C | T | 1 | a0001c0002t0001g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.740+2988C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311571 | ||||||
chr9:78311604
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.740+3021C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311604 | ||||||
chr9:78311618
|
G | A | 1 | a0001c0002t0001g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.740+3035G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311618 | ||||||
chr9:78311635
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+3052C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311635 | ||||||
chr9:78311651
|
G | A | 2 | a0001c0002t0001g0251a0001c0002t0001g0275 | 2 | HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.740+3068G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311651 | ||||||
chr9:78311780
|
C | T | 80 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0016others(77): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.740+3197C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311780 | ||||||
chr9:78311828
|
T | TCAAAAC | 76 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0025others(73): Show | 88 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.740+3245_740+3246i others(8): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311828 | ||||||
chr9:78311828
|
T | TCAAAACA others(5): Show |
16 | a0001c0002t0001g0007a0001c0002t0001g0032a0001c0002t0001g0140others(13): Show | 18 | HG01070.hp2 HG01192.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.740+3245_740+3246i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311828 | ||||||
chr9:78311829
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0025others(89): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.740+3246G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311829 | ||||||
chr9:78311829
|
G | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0095others(52): Show | 58 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.740+3246G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311829 | ||||||
chr9:78311829
|
G | GAAAACA | 5 | a0001c0001t0001g0029a0001c0001t0001g0350a0001c0001t0001g0351others(2): Show | 6 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+3274_740+3279d others(8): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78311829 | |||||
chr9:78311908
|
C | G | 1 | a0001c0002t0001g0030 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.740+3325C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311908 | ||||||
chr9:78311982
|
C | T | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3399C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311982 | ||||||
chr9:78311989
|
C | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+3406C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78311989 | ||||||
chr9:78312004
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.740+3421A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312004 | ||||||
chr9:78312047
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(145): Show | 165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.740+3464C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312047 | ||||||
chr9:78312050
|
C | CT | 7 | a0001c0001t0001g0342a0001c0001t0002g0108a0001c0001t0002g0120others(4): Show | 7 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.740+3480dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78312050 | |||||
chr9:78312062
|
TTC | T | 9 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0187others(6): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.740+3480_740+3481d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312062 | ||||||
chr9:78312063
|
TC | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(157): Show | 179 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.740+3484delC | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78312063 | |||||
chr9:78312064
|
C | T | 92 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0272others(89): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.740+3481C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312064 | ||||||
chr9:78312144
|
C | T | 2 | a0001c0002t0001g0238a0001c0002t0001g0239 | 2 | HG00733.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.740+3561C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312144 | ||||||
chr9:78312319
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0002t0001g0032others(1): Show | 6 | HG00642.hp1 HG01070.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.740+3736G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312319 | ||||||
chr9:78312323
|
G | C | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3740G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312323 | ||||||
chr9:78312375
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.740+3792A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312375 | ||||||
chr9:78312474
|
T | G | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3891T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312474 | ||||||
chr9:78312475
|
C | T | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3892C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312475 | ||||||
chr9:78312476
|
A | T | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.740+3893A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312476 | ||||||
chr9:78312493
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(107): Show | 123 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.740+3910C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312493 | ||||||
chr9:78312575
|
A | C | 36 | a0001c0001t0002g0079a0001c0002t0001g0007a0001c0002t0001g0027others(33): Show | 40 | HG00323.hp2 HG01074.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.740+3992A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312575 | ||||||
chr9:78312586
|
C | T | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.740+4003C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312586 | ||||||
chr9:78312588
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(145): Show | 165 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.740+4005C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312588 | ||||||
chr9:78312656
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740+4073A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312656 | ||||||
chr9:78312899
|
A | G | 38 | a0001c0001t0002g0079a0001c0002t0001g0007a0001c0002t0001g0027others(35): Show | 42 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.740+4316A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78312899 | ||||||
chr9:78313030
|
C | T | 38 | a0001c0001t0002g0079a0001c0002t0001g0007a0001c0002t0001g0027others(35): Show | 42 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.740+4447C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313030 | ||||||
chr9:78313103
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.740+4520C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313103 | ||||||
chr9:78313297
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.741-4379G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313297 | ||||||
chr9:78313428
|
CAG | C | 3 | a0001c0002t0001g0032a0001c0002t0001g0210a0001c0002t0001g0242 | 3 | HG01070.hp2 HG02738.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.741-4245_741-4244d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78313428 | |||||
chr9:78313448
|
C | T | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-4228C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313448 | ||||||
chr9:78313483
|
T | TGG | 38 | a0001c0001t0002g0079a0001c0002t0001g0007a0001c0002t0001g0027others(35): Show | 42 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.741-4193_741-4192i others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313483 | ||||||
chr9:78313584
|
C | T | 1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.741-4092C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313584 | ||||||
chr9:78313727
|
C | T | 1 | a0001c0002t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.741-3949C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313727 | ||||||
chr9:78313728
|
G | A | 1 | a0001c0002t0001g0221 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.741-3948G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313728 | ||||||
chr9:78313802
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0272a0001c0001t0003g0324 | 5 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.741-3874G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313802 | ||||||
chr9:78313863
|
T | C | 1 | a0001c0001t0001g0351 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.741-3813T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313863 | ||||||
chr9:78313922
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.741-3754C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313922 | ||||||
chr9:78313940
|
C | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0016others(83): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.741-3736C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78313940 | ||||||
chr9:78314027
|
G | A | 1 | a0001c0001t0003g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.741-3649G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314027 | ||||||
chr9:78314178
|
G | C | 1 | a0001c0001t0002g0061 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.741-3498G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314178 | ||||||
chr9:78314239
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.741-3437C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314239 | ||||||
chr9:78314301
|
A | ATCCTGTG others(73): Show |
36 | a0001c0001t0002g0079a0001c0002t0001g0007a0001c0002t0001g0027others(33): Show | 40 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.741-3358_741-3357i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314301 | |||||
chr9:78314301
|
A | ATCCTGTG others(73): Show |
2 | a0001c0002t0001g0146a0001c0002t0001g0337 | 2 | NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.741-3358_741-3357i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314301 | |||||
chr9:78314319
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(144): Show | 164 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.741-3357T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314319 | ||||||
chr9:78314379
|
T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(257): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.741-3297T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314379 | ||||||
chr9:78314381
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(105): Show | 121 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.741-3295A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314381 | ||||||
chr9:78314399
|
C | CCACAGGG others(73): Show |
103 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(100): Show | 110 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.741-3213_741-3212i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314399 | |||||
chr9:78314399
|
C | T | 39 | a0001c0001t0002g0041a0001c0001t0002g0079a0001c0002t0001g0007others(36): Show | 43 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.741-3277C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314399 | ||||||
chr9:78314431
|
G | T | 85 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0016others(82): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.741-3245G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314431 | ||||||
chr9:78314445
|
G | A | 1 | a0001c0002t0001g0338 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.741-3231G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314445 | ||||||
chr9:78314464
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0299a0001c0001t0001g0309others(3): Show | 12 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.741-3212T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314464 | ||||||
chr9:78314479
|
T | TCACAGGG others(73): Show |
1 | a0001c0002t0001g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.741-3132_741-3131i others(82): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314479 | |||||
chr9:78314489
|
T | TAGACATC others(70): Show |
1 | a0001c0001t0001g0309 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.741-3133_741-3132i others(79): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78314489 | |||||
chr9:78314604
|
T | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(140): Show | 154 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.741-3072T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314604 | ||||||
chr9:78314756
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0299 | 8 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.741-2920C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314756 | ||||||
chr9:78314822
|
C | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(139): Show | 153 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.741-2854C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314822 | ||||||
chr9:78314878
|
C | T | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.741-2798C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314878 | ||||||
chr9:78314968
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.741-2708T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314968 | ||||||
chr9:78314973
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0083 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.741-2703C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78314973 | ||||||
chr9:78315010
|
CA | C | 22 | a0001c0001t0002g0079a0001c0002t0001g0027a0001c0002t0001g0030others(19): Show | 24 | HG00323.hp2 HG01074.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.741-2665delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315010 | ||||||
chr9:78315069
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.741-2607G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315069 | ||||||
chr9:78315145
|
T | G | 2 | a0001c0001t0001g0314a0001c0001t0002g0313 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.741-2531T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315145 | ||||||
chr9:78315157
|
A | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0272 | 4 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-2519A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315157 | ||||||
chr9:78315278
|
T | C | 1 | a0001c0002t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.741-2398T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315278 | ||||||
chr9:78315327
|
C | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0017others(141): Show | 155 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.741-2349C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315327 | ||||||
chr9:78315343
|
T | C | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-2333T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315343 | ||||||
chr9:78315462
|
C | G | 1 | a0001c0001t0002g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.741-2214C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315462 | ||||||
chr9:78315523
|
C | T | 22 | a0001c0001t0002g0079a0001c0002t0001g0027a0001c0002t0001g0030others(19): Show | 24 | HG00323.hp2 HG01074.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.741-2153C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315523 | ||||||
chr9:78315525
|
G | A | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-2151G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315525 | ||||||
chr9:78315686
|
C | A | 84 | a0001c0002t0001g0001a0001c0002t0001g0008a0001c0002t0001g0016others(81): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.741-1990C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315686 | ||||||
chr9:78315806
|
G | A | 1 | a0001c0002t0001g0323 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.741-1870G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315806 | ||||||
chr9:78315835
|
C | T | 9 | a0001c0002t0001g0008a0001c0002t0001g0016a0001c0002t0001g0163others(6): Show | 12 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.741-1841C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315835 | ||||||
chr9:78315925
|
AT | A | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-1746delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78315925 | |||||
chr9:78315948
|
G | C | 1 | a0001c0002t0001g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.741-1728G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78315948 | ||||||
chr9:78316027
|
C | T | 3 | a0001c0002t0001g0249a0001c0002t0001g0254a0001c0002t0001g0260 | 3 | HG00423.hp1 NA18941.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.741-1649C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316027 | ||||||
chr9:78316034
|
C | A | 1 | a0001c0002t0001g0032 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.741-1642C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316034 | ||||||
chr9:78316055
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.741-1621G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316055 | ||||||
chr9:78316074
|
G | A | 1 | a0001c0002t0003g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.741-1602G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316074 | ||||||
chr9:78316134
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 5 | HG02055.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.741-1542G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316134 | ||||||
chr9:78316300
|
A | G | 2 | a0001c0002t0001g0357a0001c0002t0006g0356 | 2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.741-1376A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316300 | ||||||
chr9:78316330
|
C | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0033others(6): Show | 11 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.741-1346C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316330 | ||||||
chr9:78316380
|
C | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.741-1296C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316380 | ||||||
chr9:78316387
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.741-1289G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316387 | ||||||
chr9:78316406
|
G | A | 2 | a0001c0002t0001g0223a0001c0002t0001g0224 | 2 | NA18971.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.741-1270G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316406 | ||||||
chr9:78316442
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0272 | 4 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-1234C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316442 | ||||||
chr9:78316486
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.741-1190C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316486 | ||||||
chr9:78316608
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0242 | 2 | HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.741-1068C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316608 | ||||||
chr9:78316695
|
C | T | 4 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-981C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316695 | ||||||
chr9:78316789
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0272 | 4 | HG00642.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-887C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316789 | ||||||
chr9:78316843
|
TA | T | 3 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG01168.hp2 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.741-831delA | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78316843 | |||||
chr9:78316848
|
A | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.741-828A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316848 | ||||||
chr9:78316852
|
G | C | 2 | a0001c0002t0001g0323a0001c0002t0001g0360 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.741-824G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316852 | ||||||
chr9:78316871
|
C | T | 4 | a0001c0001t0002g0075a0001c0001t0002g0096a0001c0001t0002g0102others(1): Show | 4 | NA18961.hp1 NA19010.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-805C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316871 | ||||||
chr9:78316941
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0350others(1): Show | 5 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.741-735G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78316941 | ||||||
chr9:78317001
|
C | T | 1 | a0001c0001t0002g0102 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.741-675C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317001 | ||||||
chr9:78317088
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.741-588T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317088 | ||||||
chr9:78317173
|
T | A | 4 | a0001c0001t0002g0097a0001c0001t0002g0135a0001c0002t0001g0032others(1): Show | 4 | HG01070.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.741-503T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317173 | ||||||
chr9:78317249
|
TTTTC | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0111others(90): Show | 103 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.741-419_741-416del others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 78317249 | |||||
chr9:78317257
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.741-419C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317257 | ||||||
chr9:78317279
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0104others(94): Show | 107 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.741-397A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317279 | ||||||
chr9:78317283
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0104others(91): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.741-393C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317283 | ||||||
chr9:78317440
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.741-236C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317440 | ||||||
chr9:78317530
|
C | T | 1 | a0001c0002t0001g0237 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.741-146C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317530 | ||||||
chr9:78317599
|
C | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0104others(92): Show | 105 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.741-77C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317599 | ||||||
chr9:78317658
|
T | A | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(243): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.741-18T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 6/8 | chr9 | 78317658 | ||||||
chr9:78317873
|
T | G | 251 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(248): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.869+69T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78317873 | ||||||
chr9:78317971
|
C | T | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(247): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.869+167C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78317971 | ||||||
chr9:78318082
|
T | C | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(247): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.869+278T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318082 | ||||||
chr9:78318104
|
C | T | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(247): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.869+300C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318104 | ||||||
chr9:78318218
|
G | A | 1 | a0001c0002t0001g0279 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.869+414G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318218 | ||||||
chr9:78318508
|
A | G | 108 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(105): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.869+704A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318508 | ||||||
chr9:78318642
|
T | C | 111 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(108): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.869+838T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318642 | ||||||
chr9:78318704
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.869+900C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318704 | ||||||
chr9:78318706
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.869+902A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318706 | ||||||
chr9:78318719
|
T | C | 1 | a0005c0008t0003g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+915T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318719 | ||||||
chr9:78318757
|
A | G | 1 | a0001c0001t0001g0362 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.869+953A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318757 | ||||||
chr9:78318828
|
G | A | 26 | a0001c0001t0001g0193a0001c0001t0001g0296a0001c0001t0001g0306others(23): Show | 28 | HG01192.hp1 HG01346.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.869+1024G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318828 | ||||||
chr9:78318890
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.869+1086C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318890 | ||||||
chr9:78318997
|
T | C | 1 | a0001c0002t0001g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.869+1193T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78318997 | ||||||
chr9:78319019
|
C | T | 1 | a0001c0002t0005g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.869+1215C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319019 | ||||||
chr9:78319052
|
C | T | 16 | a0001c0001t0002g0045a0001c0001t0002g0063a0001c0001t0003g0148others(13): Show | 16 | HG01496.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.869+1248C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319052 | ||||||
chr9:78319095
|
C | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0272others(25): Show | 31 | HG00642.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.869+1291C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319095 | ||||||
chr9:78319249
|
G | A | 2 | a0001c0001t0001g0352a0001c0001t0011g0214 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.869+1445G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319249 | ||||||
chr9:78319331
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.869+1527T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319331 | ||||||
chr9:78319386
|
G | A | 1 | a0005c0008t0003g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+1582G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319386 | ||||||
chr9:78319390
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0287a0001c0001t0001g0304others(2): Show | 5 | NA18939.hp2 NA18966.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+1586G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319390 | ||||||
chr9:78319449
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.869+1645A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319449 | ||||||
chr9:78319538
|
TGTGTGAG others(7): Show |
T | 1 | a0001c0002t0002g0059 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.869+1736_869+1749d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78319538 | |||||
chr9:78319884
|
C | T | 1 | a0001c0001t0002g0114 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.869+2080C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319884 | ||||||
chr9:78319902
|
C | T | 7 | a0001c0001t0002g0118a0001c0002t0001g0209a0001c0002t0001g0220others(4): Show | 7 | NA18946.hp2 NA18954.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.869+2098C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319902 | ||||||
chr9:78319903
|
G | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0024others(61): Show | 68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.869+2099G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78319903 | ||||||
chr9:78319987
|
CTCAT | C | 104 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(101): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.869+2196_869+2199d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78319987 | |||||
chr9:78320215
|
G | A | 1 | a0001c0002t0001g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.869+2411G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320215 | ||||||
chr9:78320296
|
C | T | 104 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(101): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.869+2492C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320296 | ||||||
chr9:78320322
|
T | TTCCA | 104 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(101): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.869+2529_869+2532d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320322 | |||||
chr9:78320322
|
T | TTCCATCC others(1): Show |
129 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(126): Show | 144 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.869+2525_869+2532d others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320322 | |||||
chr9:78320322
|
T | TTCCATCC others(5): Show |
1 | a0005c0008t0003g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+2521_869+2532d others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320322 | |||||
chr9:78320333
|
C | CATCCATC others(5): Show |
11 | a0001c0001t0001g0193a0001c0001t0002g0063a0001c0001t0004g0147others(8): Show | 13 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+2532_869+2533i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320333 | |||||
chr9:78320337
|
T | C | 11 | a0001c0001t0001g0193a0001c0001t0002g0063a0001c0001t0004g0147others(8): Show | 13 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.869+2533T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320337 | ||||||
chr9:78320362
|
G | T | 3 | a0001c0001t0003g0324a0001c0001t0004g0194a0001c0002t0006g0356 | 3 | HG03471.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.869+2558G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320362 | ||||||
chr9:78320427
|
C | A | 2 | a0001c0002t0001g0358a0001c0002t0001g0359 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.869+2623C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320427 | ||||||
chr9:78320479
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.869+2675C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320479 | ||||||
chr9:78320642
|
T | TCCACCCA others(1): Show |
6 | a0001c0002t0001g0030a0001c0002t0001g0136a0001c0002t0001g0137others(3): Show | 7 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.869+2846_869+2853d others(10): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320642 | |||||
chr9:78320672
|
TGTCCATC others(9): Show |
T | 107 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0054others(104): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.869+2882_869+2897d others(18): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320672 | |||||
chr9:78320675
|
CCATCCAT others(8): Show |
C | 1 | a0001c0002t0002g0059 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.869+2873_869+2887d others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78320675 | |||||
chr9:78320699
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.869+2895C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320699 | ||||||
chr9:78320758
|
G | T | 1 | a0001c0002t0002g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.869+2954G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320758 | ||||||
chr9:78320883
|
C | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(117): Show | 132 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.869+3079C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320883 | ||||||
chr9:78320929
|
C | T | 17 | a0001c0001t0001g0296a0001c0001t0001g0306a0001c0002t0001g0146others(14): Show | 17 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.869+3125C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78320929 | ||||||
chr9:78321010
|
TC | T | 247 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(244): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.869+3214delC | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78321010 | |||||
chr9:78321016
|
C | G | 1 | a0001c0001t0002g0051 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.869+3212C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321016 | ||||||
chr9:78321241
|
C | T | 2 | a0001c0002t0001g0179a0001c0002t0002g0128 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.869+3437C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321241 | ||||||
chr9:78321402
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.869+3598T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321402 | ||||||
chr9:78321422
|
A | G | 2 | a0001c0001t0001g0154a0001c0002t0001g0323 | 2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.869+3618A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321422 | ||||||
chr9:78321483
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0350a0001c0001t0001g0351others(1): Show | 5 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+3679A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321483 | ||||||
chr9:78321708
|
T | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0024others(83): Show | 90 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.869+3904T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321708 | ||||||
chr9:78321743
|
C | T | 1 | a0001c0002t0002g0060 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.869+3939C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321743 | ||||||
chr9:78321837
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.869+4033A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321837 | ||||||
chr9:78321913
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.869+4109A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321913 | ||||||
chr9:78321913
|
AATAT | A | 6 | a0001c0001t0004g0004a0001c0001t0004g0278a0001c0002t0001g0358others(3): Show | 10 | HG01081.hp2 HG01123.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.869+4113_869+4116d others(6): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78321913 | |||||
chr9:78321914
|
A | G | 94 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0024others(91): Show | 100 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.869+4110A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78321914 | ||||||
chr9:78322114
|
T | C | 2 | a0001c0002t0001g0139a0001c0002t0003g0228 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.869+4310T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322114 | ||||||
chr9:78322151
|
T | A | 2 | a0001c0001t0001g0352a0001c0001t0011g0214 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.869+4347T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322151 | ||||||
chr9:78322358
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0272 | 5 | HG00642.hp1 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.869+4554G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322358 | ||||||
chr9:78322359
|
T | C | 1 | a0001c0001t0009g0330 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.869+4555T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322359 | ||||||
chr9:78322365
|
T | C | 4 | a0001c0001t0002g0108a0001c0001t0002g0127a0001c0002t0001g0260others(1): Show | 4 | NA18959.hp2 NA19005.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.869+4561T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322365 | ||||||
chr9:78322537
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.869+4733C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322537 | ||||||
chr9:78322994
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.870-5057T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78322994 | ||||||
chr9:78323061
|
G | T | 1 | a0001c0002t0001g0321 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.870-4990G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323061 | ||||||
chr9:78323085
|
G | A | 125 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0035others(122): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.870-4966G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323085 | ||||||
chr9:78323121
|
G | A | 6 | a0001c0001t0004g0004a0001c0001t0004g0278a0001c0002t0001g0358others(3): Show | 10 | HG01081.hp2 HG01123.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-4930G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323121 | ||||||
chr9:78323241
|
G | C | 1 | a0001c0002t0002g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.870-4810G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323241 | ||||||
chr9:78323358
|
C | A | 1 | a0001c0002t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.870-4693C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323358 | ||||||
chr9:78323401
|
G | A | 9 | a0001c0001t0001g0193a0001c0001t0001g0343a0001c0002t0001g0007others(6): Show | 11 | HG01192.hp1 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-4650G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323401 | ||||||
chr9:78323427
|
A | T | 1 | a0001c0002t0002g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.870-4624A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323427 | ||||||
chr9:78323450
|
C | T | 3 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0038 | 3 | HG01168.hp2 HG01169.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.870-4601C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323450 | ||||||
chr9:78323494
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0024others(61): Show | 68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.870-4557C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323494 | ||||||
chr9:78323539
|
C | T | 9 | a0001c0001t0001g0193a0001c0001t0001g0343a0001c0002t0001g0007others(6): Show | 11 | HG01192.hp1 HG02258.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-4512C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323539 | ||||||
chr9:78323627
|
T | G | 1 | a0001c0002t0001g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.870-4424T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323627 | ||||||
chr9:78323691
|
A | C | 1 | a0001c0002t0001g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.870-4360A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323691 | ||||||
chr9:78323703
|
G | A | 1 | a0001c0002t0003g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.870-4348G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323703 | ||||||
chr9:78323809
|
A | G | 1 | a0001c0002t0001g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.870-4242A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323809 | ||||||
chr9:78323986
|
G | A | 2 | a0001c0001t0001g0352a0001c0001t0011g0214 | 2 | HG01891.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.870-4065G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323986 | ||||||
chr9:78323999
|
C | A | 6 | a0001c0001t0004g0004a0001c0001t0004g0278a0001c0002t0001g0358others(3): Show | 10 | HG01081.hp2 HG01123.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-4052C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78323999 | ||||||
chr9:78324050
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.870-4001A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324050 | ||||||
chr9:78324083
|
G | A | 119 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0035others(116): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.870-3968G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324083 | ||||||
chr9:78324101
|
G | A | 21 | a0001c0001t0001g0296a0001c0001t0001g0306a0001c0001t0003g0324others(18): Show | 21 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.870-3950G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324101 | ||||||
chr9:78324109
|
G | A | 3 | a0001c0002t0001g0355a0001c0002t0003g0141a0001c0002t0003g0354 | 3 | HG02572.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-3942G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324109 | ||||||
chr9:78324215
|
G | A | 17 | a0001c0001t0001g0296a0001c0001t0001g0306a0001c0002t0001g0146others(14): Show | 17 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.870-3836G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324215 | ||||||
chr9:78324257
|
T | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(253): Show | 293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.870-3794T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324257 | ||||||
chr9:78324301
|
A | G | 17 | a0001c0001t0001g0296a0001c0001t0001g0306a0001c0002t0001g0146others(14): Show | 17 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.870-3750A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324301 | ||||||
chr9:78324347
|
C | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0272 | 5 | HG00642.hp1 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-3704C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324347 | ||||||
chr9:78324416
|
T | A | 16 | a0001c0001t0002g0063a0001c0001t0003g0148a0001c0001t0003g0200others(13): Show | 16 | HG01496.hp2 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.870-3635T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324416 | ||||||
chr9:78324428
|
C | G | 1 | a0001c0001t0003g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-3623C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324428 | ||||||
chr9:78324492
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.870-3559C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324492 | ||||||
chr9:78324917
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0242 | 2 | HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.870-3134G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324917 | ||||||
chr9:78324963
|
T | G | 129 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0029others(126): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.870-3088T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324963 | ||||||
chr9:78324995
|
A | G | 1 | a0001c0002t0001g0320 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.870-3056A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78324995 | ||||||
chr9:78325097
|
T | A | 76 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0024others(73): Show | 80 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.870-2954T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325097 | ||||||
chr9:78325186
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.870-2865G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325186 | ||||||
chr9:78325285
|
G | A | 1 | a0001c0001t0002g0013 | 2 | NA18945.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.870-2766G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325285 | ||||||
chr9:78325305
|
C | T | 18 | a0001c0001t0001g0296a0001c0001t0001g0306a0001c0002t0001g0146others(15): Show | 18 | HG01346.hp1 HG01346.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.870-2746C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325305 | ||||||
chr9:78325306
|
C | T | 1 | a0001c0002t0001g0357 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.870-2745C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325306 | ||||||
chr9:78325377
|
T | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0035others(10): Show | 16 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.870-2674T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325377 | ||||||
chr9:78325382
|
C | T | 1 | a0001c0002t0001g0248 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.870-2669C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325382 | ||||||
chr9:78325516
|
C | G | 3 | a0001c0002t0001g0358a0001c0002t0001g0359a0005c0008t0003g0142 | 3 | HG02717.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.870-2535C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325516 | ||||||
chr9:78325638
|
T | C | 33 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0296others(30): Show | 33 | HG01081.hp1 HG01109.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.870-2413T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325638 | ||||||
chr9:78325660
|
G | A | 19 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0296others(16): Show | 19 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.870-2391G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325660 | ||||||
chr9:78325696
|
A | T | 1 | a0001c0001t0001g0351 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.870-2355A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325696 | ||||||
chr9:78325734
|
C | T | 21 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0296others(18): Show | 21 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.870-2317C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325734 | ||||||
chr9:78325933
|
G | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(209): Show | 234 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(231): Show |
intron_variant | MODIFIER | c.870-2118G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325933 | ||||||
chr9:78325992
|
C | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0034others(93): Show | 106 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.870-2059C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78325992 | ||||||
chr9:78326025
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.870-2026G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326025 | ||||||
chr9:78326064
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0111 | 2 | NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.870-1987A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326064 | ||||||
chr9:78326129
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-1922G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326129 | ||||||
chr9:78326186
|
A | G | 11 | a0001c0001t0004g0004a0001c0001t0004g0147a0001c0001t0004g0194others(8): Show | 15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-1865A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326186 | ||||||
chr9:78326249
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.870-1802C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326249 | ||||||
chr9:78326250
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.870-1801G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326250 | ||||||
chr9:78326492
|
T | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0029others(11): Show | 18 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.870-1559T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326492 | ||||||
chr9:78326669
|
C | T | 11 | a0001c0001t0004g0004a0001c0001t0004g0147a0001c0001t0004g0194others(8): Show | 15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-1382C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326669 | ||||||
chr9:78326724
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-1327C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326724 | ||||||
chr9:78326794
|
C | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 223 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.870-1257C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326794 | ||||||
chr9:78326808
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.870-1243C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326808 | ||||||
chr9:78326845
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(82): Show | 94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.870-1206A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326845 | ||||||
chr9:78326934
|
A | AATATATA others(7): Show |
2 | a0001c0002t0003g0141a0001c0002t0003g0354 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.870-1108_870-1095d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326934 | |||||
chr9:78326934
|
AAT | A | 11 | a0001c0001t0004g0004a0001c0001t0004g0147a0001c0001t0004g0194others(8): Show | 15 | HG01081.hp2 HG01123.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-1096_870-1095d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326934 | |||||
chr9:78326953
|
A | AT | 14 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 16 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.870-1097dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326953 | |||||
chr9:78326955
|
A | AT | 9 | a0001c0001t0001g0343a0001c0001t0002g0101a0001c0002t0001g0016others(6): Show | 10 | HG00733.hp2 HG01106.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-1078dupT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATAT | 45 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0001g0145others(42): Show | 53 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(5): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(54): Show |
1 | a0001c0002t0003g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(63): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(35): Show |
1 | a0001c0002t0003g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(44): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0003g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(45): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0003g0200 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(46): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(44): Show |
1 | a0001c0002t0003g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(53): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(49): Show |
2 | a0001c0001t0003g0294a0001c0002t0003g0246 | 2 | HG02451.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(58): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0003g0310 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(62): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0003g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(44): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0003g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(47): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(42): Show |
1 | a0001c0001t0003g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(51): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(48): Show |
1 | a0001c0001t0005g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(57): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(50): Show |
1 | a0001c0001t0005g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(59): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0003g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(35): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0003g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(41): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(25): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(27): Show |
1 | a0001c0002t0003g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(36): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(36): Show |
1 | a0001c0002t0005g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(45): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(41): Show |
1 | a0001c0001t0009g0330 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(50): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(32): Show |
1 | a0001c0002t0001g0358 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(41): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(33): Show |
1 | a0001c0002t0001g0359 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(42): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(40): Show |
1 | a0001c0001t0003g0332 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(49): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0003g0250 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(52): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(54): Show |
1 | a0001c0001t0003g0290 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(63): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0139 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(25): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(44): Show |
1 | a0001c0001t0003g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(53): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(57): Show |
1 | a0001c0001t0003g0152 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(66): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(25): Show |
1 | a0005c0008t0003g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(34): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0003g0156 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(47): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0010 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(21): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(7): Show |
1 | a0001c0002t0010g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0166a0001c0001t0001g0340a0001c0002t0002g0086 | 3 | HG02523.hp1 NA18960.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(19): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0296a0001c0001t0001g0306 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(8): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0001g0176others(2): Show | 7 | HG02257.hp1 HG02258.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0024a0001c0001t0001g0264a0001c0001t0001g0265others(1): Show | 5 | HG00438.hp2 NA18747.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(19): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATTT others(5): Show |
1 | a0001c0002t0001g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATTT others(6): Show |
1 | a0001c0002t0005g0044 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(15): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATTT others(7): Show |
1 | a0001c0002t0001g0146 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATTT others(8): Show |
3 | a0001c0001t0001g0174a0001c0001t0001g0185a0002c0004t0001g0175 | 3 | NA18995.hp1 NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATTT others(9): Show |
2 | a0001c0001t0001g0297a0001c0009t0002g0116 | 2 | NA18960.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.870-1095_870-1094i others(18): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATTT others(10): Show |
10 | a0001c0001t0001g0095a0001c0001t0001g0159a0001c0001t0001g0171others(7): Show | 10 | HG00423.hp1 HG02074.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(19): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATATTT others(11): Show |
4 | a0001c0001t0001g0283a0001c0001t0001g0311a0001c0001t0001g0319others(1): Show | 4 | HG02071.hp1 NA18989.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(20): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATTTTT others(3): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0350others(1): Show | 7 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(12): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATTTTT others(4): Show |
3 | a0001c0002t0001g0018a0001c0002t0001g0347a0004c0006t0001g0326 | 4 | HG02559.hp1 HG02723.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(13): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATTTTT others(5): Show |
10 | a0001c0001t0001g0111a0001c0001t0001g0302a0001c0002t0001g0212others(7): Show | 10 | HG01346.hp1 HG01952.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATTTTT others(6): Show |
4 | a0001c0001t0001g0104a0001c0002t0001g0149a0001c0002t0001g0182others(1): Show | 4 | NA18953.hp1 NA18956.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(15): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATTTTT others(7): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0172a0001c0001t0001g0285others(2): Show | 6 | HG00621.hp2 HG00673.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATTTTT others(8): Show |
11 | a0001c0001t0001g0157a0001c0001t0001g0164a0001c0001t0001g0173others(8): Show | 11 | HG00558.hp2 HG00673.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(17): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATATTTTT others(9): Show |
1 | a0001c0001t0001g0165 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.870-1095_870-1094i others(18): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATT | 6 | a0001c0001t0001g0028a0001c0001t0001g0184a0001c0001t0001g0299others(3): Show | 6 | HG02965.hp2 HG03209.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1079_870-1078d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.870-1087_870-1078d others(12): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0351a0001c0002t0001g0355 | 2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.870-1088_870-1078d others(13): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0195a0001c0002t0001g0357 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.870-1090_870-1078d others(15): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0030 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.870-1091_870-1078d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326955
|
A | T | 43 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(40): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.870-1096A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326955 | ||||||
chr9:78326955
|
AT | A | 6 | a0001c0001t0002g0067a0001c0001t0002g0133a0001c0002t0001g0232others(3): Show | 6 | HG01070.hp1 HG01515.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1078delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78326955 | |||||
chr9:78326956
|
T | TA | 7 | a0001c0001t0002g0075a0001c0002t0001g0226a0001c0002t0001g0231others(4): Show | 7 | HG01099.hp2 HG01257.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(3): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326956 | ||||||
chr9:78326956
|
T | TATA | 15 | a0001c0001t0001g0168a0001c0001t0001g0216a0001c0001t0001g0217others(12): Show | 15 | HG00423.hp2 HG02135.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.870-1095_870-1094i others(5): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326956 | ||||||
chr9:78326957
|
T | A | 21 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0262others(18): Show | 22 | HG00621.hp1 HG01070.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.870-1094T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326957 | ||||||
chr9:78326958
|
T | A | 6 | a0001c0001t0001g0216a0001c0001t0001g0266a0001c0001t0002g0122others(3): Show | 6 | HG00423.hp2 HG03710.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-1093T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326958 | ||||||
chr9:78326959
|
T | A | 1 | a0001c0001t0001g0309 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.870-1092T>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78326959 | ||||||
chr9:78327013
|
T | C | 1 | a0001c0001t0003g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-1038T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327013 | ||||||
chr9:78327042
|
A | G | 330 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 376 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(373): Show |
intron_variant | MODIFIER | c.870-1009A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327042 | ||||||
chr9:78327130
|
AT | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(82): Show | 94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.870-910delT | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 78327130 | |||||
chr9:78327149
|
G | A | 1 | a0001c0001t0003g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.870-902G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327149 | ||||||
chr9:78327196
|
C | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 220 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(217): Show |
intron_variant | MODIFIER | c.870-855C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327196 | ||||||
chr9:78327213
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.870-838G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327213 | ||||||
chr9:78327225
|
T | G | 1 | a0001c0002t0001g0348 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.870-826T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327225 | ||||||
chr9:78327284
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-767C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327284 | ||||||
chr9:78327348
|
A | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 239 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.870-703A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327348 | ||||||
chr9:78327409
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.870-642A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327409 | ||||||
chr9:78327489
|
T | C | 3 | a0001c0001t0001g0010a0001c0002t0001g0136a0001c0002t0001g0137 | 4 | HG02257.hp1 HG02258.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-562T>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327489 | ||||||
chr9:78327759
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.870-292C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327759 | ||||||
chr9:78327912
|
G | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(201): Show | 224 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.870-139G>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327912 | ||||||
chr9:78327913
|
G | A | 21 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0296others(18): Show | 21 | HG01346.hp1 HG01515.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.870-138G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78327913 | ||||||
chr9:78328005
|
C | G | 1 | a0001c0001t0001g0287 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.870-46C>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 7/8 | chr9 | 78328005 | ||||||
chr9:78328355
|
A | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(82): Show | 94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1007+167A>C | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328355 | ||||||
chr9:78328356
|
C | A | 1 | a0001c0002t0001g0279 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1007+168C>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328356 | ||||||
chr9:78328513
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1007+325A>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328513 | ||||||
chr9:78328520
|
TTATTATT others(5): Show |
T | 8 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0035others(5): Show | 11 | HG00642.hp1 HG01255.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1007+334_1007+345d others(14): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 78328520 | |||||
chr9:78328584
|
C | T | 25 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0296others(22): Show | 27 | HG01243.hp2 HG01346.hp1 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.1007+396C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328584 | ||||||
chr9:78328605
|
GGAATGTC others(7): Show |
G | 214 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1008-373_1008-360d others(16): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 78328605 | |||||
chr9:78328623
|
AAT | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1008-356_1008-355d others(4): Show |
PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 78328623 | |||||
chr9:78328626
|
A | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 238 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1008-355A>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328626 | ||||||
chr9:78328685
|
G | A | 30 | a0001c0001t0003g0148a0001c0001t0003g0150a0001c0001t0003g0151others(27): Show | 30 | HG00738.hp2 HG01081.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.1008-296G>A | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328685 | ||||||
chr9:78328704
|
C | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 222 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.1008-277C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328704 | ||||||
chr9:78328821
|
C | T | 47 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0024others(44): Show | 52 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1008-160C>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328821 | ||||||
chr9:78328946
|
T | G | 1 | a0001c0001t0002g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1008-35T>G | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328946 | ||||||
chr9:78328970
|
G | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0300 | 3 | HG02083.hp2 HG02602.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1008-11G>T | PSAT1 | ENSG00000135069.14 | transcript | ENST00000376588.4 | protein_coding | 8/8 | chr9 | 78328970 |