geneid | 466 |
---|---|
ensemblid | ENSG00000123268.9 |
hgncid | 783 |
symbol | ATF1 |
name | activating transcription factor 1 |
refseq_nuc | NM_005171.5 |
refseq_prot | NP_005162.1 |
ensembl_nuc | ENST00000262053.8 |
ensembl_prot | ENSP00000262053.3 |
mane_status | MANE Select |
chr | chr12 |
start | 50764101 |
end | 50821162 |
strand | + |
ver | v1.2 |
region | chr12:50764101-50821162 |
region5000 | chr12:50759101-50826162 |
regionname0 | ATF1_chr12_50764101_50821162 |
regionname5000 | ATF1_chr12_50759101_50826162 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 816 | 228 | 41 | 44 | 122 | 3 | 17 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
c0002 | 0/1 | 816 | 138 | 45 | 17 | 54 | 5 | 16 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
c0003 | 0/0 | 816 | 12 | 1 | 4 | 0 | 2 | 5 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
c0004 | 0/0 | 816 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
c0005 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
c0006 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
c0007 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1597 | 126 | 33 | 26 | 55 | 0 | 12 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0002 | 0/1 | 1597 | 118 | 27 | 16 | 53 | 5 | 16 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0003 | 1/0 | 1597 | 87 | 6 | 13 | 63 | 0 | 4 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0004 | 0/0 | 1599 | 25 | 4 | 9 | 1 | 5 | 6 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0005 | 0/0 | 1598 | 6 | 6 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0006 | 0/0 | 1597 | 5 | 5 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0007 | 0/0 | 1597 | 3 | 3 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0008 | 0/0 | 1597 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0009 | 0/0 | 1601 | 2 | 2 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0010 | 0/0 | 1597 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0011 | 0/0 | 1598 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0012 | 0/0 | 1598 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0013 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0014 | 0/0 | 1597 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0015 | 0/0 | 1601 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0016 | 0/0 | 1598 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
t0017 | 0/0 | 1598 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 816 | 228 | 41 | 44 | 122 | 3 | 17 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002 | 0/1 | 816 | 138 | 45 | 17 | 54 | 5 | 16 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0003 | 0/0 | 816 | 12 | 1 | 4 | 0 | 2 | 5 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0004 | 0/0 | 816 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0006 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0007 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0002c0005 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2412 | 115 | 23 | 25 | 55 | 0 | 12 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0003 | 1/0 | 2412 | 87 | 6 | 13 | 63 | 0 | 4 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0004 | 0/0 | 2414 | 12 | 2 | 5 | 1 | 3 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0005 | 0/0 | 2413 | 6 | 6 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0008 | 0/0 | 2412 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0009 | 0/0 | 2416 | 2 | 2 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0012 | 0/0 | 2413 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0015 | 0/0 | 2416 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0016 | 0/0 | 2413 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0001t0017 | 0/0 | 2413 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0001 | 0/0 | 2412 | 9 | 8 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0002 | 0/1 | 2412 | 116 | 26 | 15 | 53 | 5 | 16 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0004 | 0/0 | 2414 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0006 | 0/0 | 2412 | 5 | 5 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0007 | 0/0 | 2412 | 3 | 3 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0010 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0011 | 0/0 | 2413 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0013 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0002t0014 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0003t0004 | 0/0 | 2414 | 12 | 1 | 4 | 0 | 2 | 5 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0004t0002 | 0/0 | 2412 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0006t0001 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0001c0007t0002 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
a0002c0005t0001 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | copy fasta | chr12 | 50759101 | 50826162 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0015g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0016g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0001t0017g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0191 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0010g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0011g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0013g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0002t0014g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0003t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0004t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0006t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0001c0007t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
a0002c0005t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0196 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00099 | hp2 | a0001 | c0003 | t0004 | g0353 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0339 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0159 | EUR | GBR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0342 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0329 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01071 | hp2 | a0001 | c0004 | t0002 | g0199 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0347 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0172 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0349 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0122 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0168 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01192 | hp1 | a0001 | c0003 | t0004 | g0341 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01243 | hp1 | a0001 | c0003 | t0004 | g0352 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01243 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01256 | hp2 | a0001 | c0003 | t0004 | g0348 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0351 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0188 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0174 | EUR | IBS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01517 | hp2 | a0001 | c0003 | t0004 | g0354 | EUR | IBS | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0166 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0338 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0200 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0346 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0316 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0163 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CDX | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02257 | hp2 | a0001 | c0002 | t0006 | g0295 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0164 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0340 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02300 | hp2 | a0001 | c0002 | t0010 | g0206 | AMR | PEL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02602 | hp1 | a0001 | c0003 | t0004 | g0344 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02622 | hp2 | a0001 | c0002 | t0014 | g0327 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0332 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02683 | hp1 | a0001 | c0003 | t0004 | g0360 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0180 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0356 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0305 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02809 | hp1 | a0001 | c0007 | t0002 | g0319 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02809 | hp2 | a0002 | c0005 | t0001 | g0333 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0115 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0330 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0361 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0334 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0144 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0325 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0182 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | GWD | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03130 | hp2 | a0001 | c0006 | t0001 | g0326 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0362 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03209 | hp1 | a0001 | c0002 | t0006 | g0306 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0139 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03239 | hp2 | a0001 | c0003 | t0004 | g0359 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03453 | hp1 | a0001 | c0002 | t0007 | g0296 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0165 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0207 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03516 | hp2 | a0001 | c0002 | t0006 | g0304 | AFR | ESN | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03654 | hp1 | a0001 | c0003 | t0004 | g0358 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03688 | hp1 | a0001 | c0003 | t0004 | g0357 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0135 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0193 | SAS | BEB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0157 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0167 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0128 | SAS | STU | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18522 | hp1 | a0001 | c0002 | t0013 | g0303 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0150 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | CHB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0173 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18967 | hp2 | a0001 | c0002 | t0011 | g0209 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18989 | hp1 | a0001 | c0001 | t0008 | g0248 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19080 | hp2 | a0001 | c0001 | t0008 | g0250 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19084 | hp2 | a0001 | c0001 | t0016 | g0008 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0145 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | YRI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | ASW | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ASW | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0017 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0205 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0350 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0012 | EUR | TSI | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0161 | SAS | GIH | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01123 | hp1 | a0001 | c0003 | t0004 | g0345 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02109 | hp2 | a0001 | c0002 | t0006 | g0301 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02486 | hp1 | a0001 | c0002 | t0007 | g0298 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03471 | hp1 | a0001 | c0002 | t0006 | g0302 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | MSL | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20300 | hp1 | a0001 | c0003 | t0004 | g0309 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA20300 | hp2 | a0001 | c0001 | t0017 | g0280 | AFR | USA | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA21309 | hp1 | a0001 | c0002 | t0007 | g0297 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | LWK | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0191 | REF | REF | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0038 | REF | REF | ATF1_chr12_50759101_50826162 | ATF1 | chr12 | 50759101 | 50826162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:50814067
|
A | G | 1 | a0002 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.386A>G | p.Gln129Arg | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 5/7 | 599/2412 | 386/816 | 129/271 | chr12 | 50814067 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:50780190
|
A | G | 1 | a0001c0007 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.45A>G | p.Gln15Gln | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/7 | 258/2412 | 45/816 | 15/271 | chr12 | 50780190 | ||
chr12:50795950
|
C | T | 1 | a0001c0006 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.135C>T | p.Ser45Ser | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/7 | 348/2412 | 135/816 | 45/271 | chr12 | 50795950 | ||
chr12:50809588
|
C | T | 5 | a0001c0002a0001c0004a0001c0006others(2): Show | 142 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(139): Show |
splice_region_variant&synonymous_variant | LOW | c.327C>T | p.Tyr109Tyr | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/7 | 540/2412 | 327/816 | 109/271 | chr12 | 50809588 | ||
chr12:50814143
|
C | T | 1 | a0001c0004 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.462C>T | p.Thr154Thr | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 5/7 | 675/2412 | 462/816 | 154/271 | chr12 | 50814143 | ||
chr12:50819650
|
A | G | 1 | a0001c0003 | 12 | HG00099.hp2 HG01123.hp1 HG01192.hp1 others(9): Show |
synonymous_variant | LOW | c.687A>G | p.Glu229Glu | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 900/2412 | 687/816 | 229/271 | chr12 | 50819650 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:50819804
|
T | G | 1 | a0001c0001t0008 | 2 | NA18989.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 25 | chr12 | 50819804 | |||||
chr12:50819961
|
G | A | 1 | a0001c0002t0007 | 3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*182G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 182 | chr12 | 50819961 | |||||
chr12:50819982
|
T | C | 6 | a0001c0001t0009a0001c0002t0002a0001c0002t0010others(3): Show | 122 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*203T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 203 | chr12 | 50819982 | |||||
chr12:50820100
|
A | AT | 1 | a0001c0001t0005 | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*329dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 330 | INFO_REALIGN_3_PRIME | chr12 | 50820100 | ||||
chr12:50820157
|
T | G | 1 | a0001c0001t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 378 | chr12 | 50820157 | |||||
chr12:50820174
|
A | ATG | 3 | a0001c0001t0004a0001c0002t0004a0001c0003t0004 | 25 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*411_*412dupGT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 413 | INFO_REALIGN_3_PRIME | chr12 | 50820174 | ||||
chr12:50820484
|
G | A | 2 | a0001c0002t0006a0001c0002t0013 | 6 | HG02109.hp2 HG02257.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 705 | chr12 | 50820484 | |||||
chr12:50820485
|
G | GT | 4 | a0001c0001t0012a0001c0001t0016a0001c0001t0017others(1): Show | 4 | HG01243.hp2 NA18967.hp2 NA19084.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*713dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 714 | INFO_REALIGN_3_PRIME | chr12 | 50820485 | ||||
chr12:50820544
|
G | T | 21 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(18): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*765G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 765 | chr12 | 50820544 | |||||
chr12:50820747
|
A | ATGTT | 2 | a0001c0001t0009a0001c0001t0015 | 3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*969_*972dupTGTT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 973 | INFO_REALIGN_3_PRIME | chr12 | 50820747 | ||||
chr12:50820759
|
A | G | 1 | a0001c0002t0014 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 980 | chr12 | 50820759 | |||||
chr12:50820836
|
C | G | 1 | a0001c0002t0013 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1057C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 1057 | chr12 | 50820836 | |||||
chr12:50820844
|
G | A | 1 | a0001c0002t0010 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1065G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 7/7 | 1065 | chr12 | 50820844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:50764334
|
C | T | 2 | a0001c0001t0003g0361a0001c0001t0003g0362 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-7+27C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764334 | ||||||
chr12:50764403
|
T | C | 1 | a0001c0002t0002g0018 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-7+96T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764403 | ||||||
chr12:50764406
|
T | TG | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0002g0002others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+104dupG | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50764406 | |||||
chr12:50764479
|
C | T | 27 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(24): Show | 28 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+172C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764479 | ||||||
chr12:50764501
|
G | T | 10 | a0001c0002t0001g0325a0001c0002t0001g0328a0001c0002t0001g0329others(7): Show | 10 | HG01071.hp1 HG02109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+194G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764501 | ||||||
chr12:50764510
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+203C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764510 | ||||||
chr12:50764576
|
C | A | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-7+269C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764576 | ||||||
chr12:50764615
|
C | T | 1 | a0001c0001t0005g0316 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7+308C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764615 | ||||||
chr12:50764693
|
C | T | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18955.hp2 NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-7+386C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764693 | ||||||
chr12:50764765
|
C | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-7+458C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764765 | ||||||
chr12:50764797
|
T | A | 1 | a0001c0001t0003g0022 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-7+490T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764797 | ||||||
chr12:50764871
|
G | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(8): Show | 13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+564G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764871 | ||||||
chr12:50764933
|
A | G | 2 | a0001c0002t0004g0305a0001c0002t0006g0306 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-7+626A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764933 | ||||||
chr12:50764992
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-7+685T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50764992 | ||||||
chr12:50765076
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-7+769A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765076 | ||||||
chr12:50765227
|
A | G | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7+920A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765227 | ||||||
chr12:50765357
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-7+1050A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765357 | ||||||
chr12:50765442
|
G | C | 4 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0025others(1): Show | 5 | NA18951.hp1 NA18966.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+1135G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765442 | ||||||
chr12:50765477
|
A | C | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1170A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765477 | ||||||
chr12:50765478
|
T | A | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1171T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765478 | ||||||
chr12:50765479
|
A | C | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1172A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765479 | ||||||
chr12:50765483
|
G | A | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1176G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765483 | ||||||
chr12:50765484
|
G | T | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1177G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765484 | ||||||
chr12:50765485
|
T | C | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1178T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765485 | ||||||
chr12:50765487
|
T | C | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1180T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765487 | ||||||
chr12:50765495
|
T | G | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1188T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765495 | ||||||
chr12:50765497
|
G | T | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1190G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765497 | ||||||
chr12:50765513
|
T | TTTTG | 6 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0003g0029others(3): Show | 6 | NA18949.hp1 NA18964.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+1226_-7+1229dup others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50765513 | |||||
chr12:50765770
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(243): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-7+1463C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50765770 | ||||||
chr12:50766268
|
A | T | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+1961A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766268 | ||||||
chr12:50766424
|
G | A | 1 | a0001c0002t0006g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7+2117G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766424 | ||||||
chr12:50766424
|
G | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-7+2117G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766424 | ||||||
chr12:50766511
|
CT | C | 13 | a0001c0001t0001g0307a0001c0001t0001g0317a0001c0001t0001g0318others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7+2216delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50766511 | |||||
chr12:50766554
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-7+2247T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766554 | ||||||
chr12:50766664
|
A | G | 5 | a0001c0001t0003g0011a0001c0001t0003g0091a0001c0001t0003g0092others(2): Show | 6 | HG01975.hp1 HG02071.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+2357A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766664 | ||||||
chr12:50766750
|
G | C | 1 | a0001c0002t0002g0095 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-7+2443G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766750 | ||||||
chr12:50766829
|
A | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(360): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-7+2522A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766829 | ||||||
chr12:50766892
|
G | A | 1 | a0001c0002t0002g0096 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-7+2585G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766892 | ||||||
chr12:50766932
|
C | T | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-7+2625C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766932 | ||||||
chr12:50766947
|
A | T | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7+2640A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50766947 | ||||||
chr12:50767090
|
C | A | 1 | a0001c0001t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7+2783C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767090 | ||||||
chr12:50767092
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-7+2785A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767092 | ||||||
chr12:50767220
|
T | TA | 117 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-7+2926dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50767220 | |||||
chr12:50767236
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-7+2929A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767236 | ||||||
chr12:50767277
|
G | A | 9 | a0001c0002t0002g0032a0001c0002t0002g0097a0001c0002t0002g0098others(6): Show | 9 | NA18944.hp1 NA18950.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+2970G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767277 | ||||||
chr12:50767291
|
G | C | 1 | a0001c0001t0003g0039 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-7+2984G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767291 | ||||||
chr12:50767556
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-7+3249C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767556 | ||||||
chr12:50767604
|
A | G | 2 | a0001c0003t0004g0359a0001c0003t0004g0360 | 2 | HG02683.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-7+3297A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767604 | ||||||
chr12:50767610
|
C | G | 3 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG00597.hp2 NA19003.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-7+3303C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767610 | ||||||
chr12:50767875
|
C | CT | 13 | a0001c0001t0003g0010a0001c0001t0003g0081a0001c0001t0003g0082others(10): Show | 14 | HG00738.hp1 HG01261.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+3583dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50767875 | |||||
chr12:50767884
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+3577T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767884 | ||||||
chr12:50767954
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-7+3647C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767954 | ||||||
chr12:50767961
|
C | T | 44 | a0001c0002t0002g0012a0001c0002t0002g0095a0001c0002t0002g0167others(41): Show | 45 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.-7+3654C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767961 | ||||||
chr12:50767987
|
G | C | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7+3680G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50767987 | ||||||
chr12:50768029
|
C | T | 1 | a0001c0002t0002g0104 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-7+3722C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768029 | ||||||
chr12:50768092
|
C | G | 1 | a0001c0001t0003g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-7+3785C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768092 | ||||||
chr12:50768092
|
C | T | 1 | a0001c0002t0002g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-7+3785C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768092 | ||||||
chr12:50768186
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+3879C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768186 | ||||||
chr12:50768358
|
G | A | 1 | a0001c0002t0001g0299 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-7+4051G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768358 | ||||||
chr12:50768606
|
G | C | 1 | a0001c0002t0002g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-7+4299G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768606 | ||||||
chr12:50768657
|
A | C | 2 | a0001c0001t0009g0164a0001c0001t0009g0165 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-7+4350A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768657 | ||||||
chr12:50768669
|
CAA | C | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-7+4366_-7+4367del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50768669 | |||||
chr12:50768886
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-7+4579G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50768886 | ||||||
chr12:50769318
|
A | G | 1 | a0001c0001t0015g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-7+5011A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769318 | ||||||
chr12:50769380
|
C | T | 2 | a0001c0001t0005g0036a0001c0001t0005g0037 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-7+5073C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769380 | ||||||
chr12:50769398
|
C | T | 1 | a0001c0002t0002g0162 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-7+5091C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769398 | ||||||
chr12:50769568
|
T | C | 1 | a0001c0001t0003g0040 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-7+5261T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769568 | ||||||
chr12:50769638
|
T | G | 1 | a0001c0002t0001g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-7+5331T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769638 | ||||||
chr12:50769828
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0284a0001c0001t0001g0285others(5): Show | 9 | HG00735.hp1 HG01928.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+5521A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769828 | ||||||
chr12:50769849
|
G | A | 1 | a0001c0001t0009g0164 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7+5542G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50769849 | ||||||
chr12:50770006
|
T | C | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7+5699T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770006 | ||||||
chr12:50770375
|
G | T | 3 | a0001c0001t0003g0077a0001c0001t0003g0078a0001c0001t0003g0079 | 3 | HG02074.hp2 NA18940.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-7+6068G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770375 | ||||||
chr12:50770471
|
G | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(360): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-7+6164G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770471 | ||||||
chr12:50770506
|
G | A | 8 | a0001c0002t0002g0018a0001c0002t0002g0105a0001c0002t0002g0106others(5): Show | 8 | HG02056.hp1 HG02155.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+6199G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770506 | ||||||
chr12:50770580
|
T | C | 1 | a0001c0002t0002g0168 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-7+6273T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770580 | ||||||
chr12:50770809
|
G | C | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+6502G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770809 | ||||||
chr12:50770992
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-7+6685C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50770992 | ||||||
chr12:50770999
|
C | CT | 11 | a0001c0001t0003g0010a0001c0001t0003g0081a0001c0001t0003g0082others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+6702dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50770999 | |||||
chr12:50771027
|
A | G | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-7+6720A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771027 | ||||||
chr12:50771092
|
G | A | 3 | a0001c0002t0002g0169a0001c0002t0002g0170a0001c0002t0002g0171 | 3 | HG00597.hp1 HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-7+6785G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771092 | ||||||
chr12:50771207
|
T | G | 1 | a0001c0002t0002g0111 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-7+6900T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771207 | ||||||
chr12:50771492
|
C | G | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7+7185C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771492 | ||||||
chr12:50771656
|
A | T | 1 | a0001c0001t0005g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7+7349A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771656 | ||||||
chr12:50771714
|
G | C | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7+7407G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771714 | ||||||
chr12:50771836
|
G | A | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+7529G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771836 | ||||||
chr12:50771861
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-7+7554C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771861 | ||||||
chr12:50771912
|
G | A | 2 | a0001c0002t0002g0172a0001c0002t0002g0173 | 2 | HG01081.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+7605G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771912 | ||||||
chr12:50771949
|
T | A | 1 | a0001c0001t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7+7642T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50771949 | ||||||
chr12:50772020
|
G | A | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7+7713G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772020 | ||||||
chr12:50772102
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0015others(56): Show | 63 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.-7+7795G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772102 | ||||||
chr12:50772204
|
C | A | 1 | a0001c0002t0001g0325 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7+7897C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772204 | ||||||
chr12:50772318
|
CT | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(242): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-6-7804delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772318 | |||||
chr12:50772318
|
CTT | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 11 | HG01167.hp2 HG01256.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6-7805_-6-7804del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772318 | |||||
chr12:50772391
|
G | A | 363 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(360): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-6-7749G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772391 | ||||||
chr12:50772421
|
G | T | 2 | a0001c0002t0002g0172a0001c0002t0002g0173 | 2 | HG01081.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-7719G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772421 | ||||||
chr12:50772645
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6-7495G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772645 | ||||||
chr12:50772676
|
T | C | 1 | a0001c0002t0002g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-6-7464T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772676 | ||||||
chr12:50772676
|
T | TTC | 4 | a0001c0001t0001g0324a0001c0001t0003g0046a0001c0002t0002g0177others(1): Show | 4 | HG00733.hp1 HG00735.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-7446_-6-7445dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772676 | |||||
chr12:50772676
|
TTC | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-7446_-6-7445del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50772676 | |||||
chr12:50772678
|
C | T | 1 | a0001c0002t0002g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-6-7462C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772678 | ||||||
chr12:50772812
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-6-7328G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772812 | ||||||
chr12:50772816
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-7324A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772816 | ||||||
chr12:50772825
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-6-7315T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772825 | ||||||
chr12:50772921
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-6-7219C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50772921 | ||||||
chr12:50773030
|
T | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-7110T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773030 | ||||||
chr12:50773410
|
A | G | 1 | a0001c0002t0001g0334 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-6-6730A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773410 | ||||||
chr12:50773444
|
C | CT | 203 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(200): Show | 211 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.-6-6674dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773444 | |||||
chr12:50773444
|
C | CTT | 50 | a0001c0001t0001g0016a0001c0001t0001g0210a0001c0001t0001g0215others(47): Show | 52 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.-6-6675_-6-6674dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773444 | |||||
chr12:50773466
|
T | C | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-6-6674T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773466 | ||||||
chr12:50773466
|
T | TC | 3 | a0001c0002t0002g0179a0001c0002t0002g0180a0001c0002t0002g0181 | 3 | HG01433.hp2 HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-6-6673dupC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773466 | |||||
chr12:50773486
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-6-6654A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773486 | ||||||
chr12:50773591
|
A | AT | 117 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0009g0164others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-6-6538dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50773591 | |||||
chr12:50773632
|
C | T | 3 | a0001c0002t0002g0169a0001c0002t0002g0170a0001c0002t0002g0171 | 3 | HG00597.hp1 HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-6-6508C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773632 | ||||||
chr12:50773688
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-6452C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773688 | ||||||
chr12:50773835
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-6305C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773835 | ||||||
chr12:50773889
|
C | A | 6 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-6251C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773889 | ||||||
chr12:50773931
|
G | A | 7 | a0001c0001t0001g0118a0001c0002t0002g0111a0001c0002t0002g0116others(4): Show | 7 | HG00609.hp1 NA18942.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-6209G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50773931 | ||||||
chr12:50774286
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-6-5854C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774286 | ||||||
chr12:50774308
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-6-5832T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774308 | ||||||
chr12:50774324
|
C | T | 1 | a0001c0002t0007g0298 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-6-5816C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774324 | ||||||
chr12:50774326
|
C | T | 1 | a0001c0001t0008g0250 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-6-5814C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774326 | ||||||
chr12:50774377
|
C | T | 1 | a0001c0002t0002g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-6-5763C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774377 | ||||||
chr12:50774381
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-6-5759G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774381 | ||||||
chr12:50774678
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-6-5462G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774678 | ||||||
chr12:50774690
|
GTTTATGA others(23): Show |
G | 1 | a0001c0001t0003g0041 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-6-5447_-6-5418del others(30): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774690 | |||||
chr12:50774692
|
TTA | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-5446_-6-5445del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774692 | |||||
chr12:50774752
|
G | GT | 110 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0218others(107): Show | 118 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.-6-5375dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774752 | |||||
chr12:50774752
|
G | GTT | 6 | a0001c0001t0003g0046a0001c0001t0003g0071a0001c0001t0003g0072others(3): Show | 6 | HG02071.hp1 NA18953.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-5376_-6-5375dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50774752 | |||||
chr12:50774770
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6-5370C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774770 | ||||||
chr12:50774834
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-5306G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774834 | ||||||
chr12:50774857
|
C | T | 2 | a0001c0001t0008g0248a0001c0001t0008g0250 | 2 | NA18989.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-6-5283C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774857 | ||||||
chr12:50774872
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-5268C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774872 | ||||||
chr12:50774873
|
G | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(243): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-6-5267G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774873 | ||||||
chr12:50774986
|
C | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-5154C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50774986 | ||||||
chr12:50775082
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-5058A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775082 | ||||||
chr12:50775325
|
T | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(243): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-6-4815T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775325 | ||||||
chr12:50775335
|
G | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-4805G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775335 | ||||||
chr12:50775458
|
C | T | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-6-4682C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775458 | ||||||
chr12:50775565
|
G | GT | 10 | a0001c0001t0001g0210a0001c0001t0001g0315a0001c0001t0003g0045others(7): Show | 10 | HG00438.hp1 HG01978.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6-4563dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50775565 | |||||
chr12:50775567
|
T | G | 7 | a0001c0002t0004g0305a0001c0002t0006g0295a0001c0002t0006g0301others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-4573T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775567 | ||||||
chr12:50775612
|
G | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0310a0001c0001t0001g0311others(1): Show | 5 | HG01167.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-4528G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775612 | ||||||
chr12:50775659
|
G | A | 3 | a0001c0002t0002g0169a0001c0002t0002g0170a0001c0002t0002g0171 | 3 | HG00597.hp1 HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-6-4481G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775659 | ||||||
chr12:50775707
|
A | G | 3 | a0001c0002t0002g0151a0001c0002t0002g0152a0001c0002t0002g0153 | 3 | HG01884.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-6-4433A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775707 | ||||||
chr12:50775931
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-6-4209G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775931 | ||||||
chr12:50775964
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-6-4176A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50775964 | ||||||
chr12:50776028
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-6-4112T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776028 | ||||||
chr12:50776087
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0002g0002others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-4053C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776087 | ||||||
chr12:50776092
|
C | T | 1 | a0001c0002t0002g0205 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-6-4048C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776092 | ||||||
chr12:50776094
|
T | C | 3 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-6-4046T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776094 | ||||||
chr12:50776109
|
A | G | 4 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(1): Show | 4 | HG02559.hp2 HG02698.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-4031A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776109 | ||||||
chr12:50776205
|
A | G | 3 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-6-3935A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776205 | ||||||
chr12:50776294
|
T | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-3846T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776294 | ||||||
chr12:50776302
|
T | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-3838T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776302 | ||||||
chr12:50776310
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0311 | 3 | HG01167.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-6-3830T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776310 | ||||||
chr12:50776326
|
A | AAAAAAAT others(302): Show |
24 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(21): Show | 25 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(309): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | |||||
chr12:50776326
|
A | AAAAAAAT others(302): Show |
1 | a0001c0001t0004g0349 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(309): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | |||||
chr12:50776326
|
A | AAAAAAAT others(302): Show |
1 | a0001c0001t0004g0350 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(309): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | |||||
chr12:50776326
|
A | AAAAAAAT others(303): Show |
8 | a0001c0001t0001g0337a0001c0001t0001g0355a0001c0001t0004g0017others(5): Show | 9 | HG00099.hp2 HG00639.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-3799_-6-3798ins others(310): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776326 | |||||
chr12:50776332
|
A | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0282a0001c0001t0001g0294 | 3 | HG00733.hp2 HG01081.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-6-3808A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776332 | ||||||
chr12:50776333
|
T | A | 115 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(112): Show | 116 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-6-3807T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776333 | ||||||
chr12:50776493
|
T | TA | 25 | a0001c0001t0003g0047a0001c0001t0003g0074a0001c0001t0015g0163others(22): Show | 25 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6-3628dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776493 | |||||
chr12:50776493
|
TA | T | 10 | a0001c0001t0001g0215a0001c0001t0001g0310a0001c0001t0001g0321others(7): Show | 10 | HG01074.hp2 HG01256.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-3628delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50776493 | |||||
chr12:50776510
|
A | G | 2 | a0001c0001t0003g0022a0001c0001t0003g0046 | 2 | HG02129.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-6-3630A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776510 | ||||||
chr12:50776639
|
A | T | 1 | a0001c0002t0002g0204 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-6-3501A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50776639 | ||||||
chr12:50777252
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-6-2888G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777252 | ||||||
chr12:50777307
|
A | G | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-6-2833A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777307 | ||||||
chr12:50777441
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-6-2699C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777441 | ||||||
chr12:50777539
|
C | T | 1 | a0001c0001t0015g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-6-2601C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777539 | ||||||
chr12:50777620
|
A | AC | 24 | a0001c0001t0003g0070a0001c0001t0004g0346a0001c0002t0001g0299others(21): Show | 24 | HG00673.hp1 HG01071.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.-6-2512dupC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777620 | |||||
chr12:50777732
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(8): Show | 13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-2408G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777732 | ||||||
chr12:50777780
|
C | CA | 218 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(215): Show | 226 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-6-2347dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777780 | |||||
chr12:50777780
|
C | CAA | 41 | a0001c0001t0001g0016a0001c0001t0001g0256a0001c0001t0001g0257others(38): Show | 43 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.-6-2348_-6-2347dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777780 | |||||
chr12:50777891
|
C | A | 3 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051 | 3 | HG00642.hp1 HG01934.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-6-2249C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777891 | ||||||
chr12:50777917
|
G | A | 2 | a0001c0002t0002g0002a0001c0002t0002g0021 | 4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-2223G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50777917 | ||||||
chr12:50777936
|
CT | C | 41 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0281others(38): Show | 43 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.-6-2186delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777936 | |||||
chr12:50777936
|
CTT | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(233): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-6-2187_-6-2186del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50777936 | |||||
chr12:50778044
|
G | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6-2096G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778044 | ||||||
chr12:50778159
|
T | C | 3 | a0001c0002t0002g0097a0001c0002t0002g0099a0001c0002t0002g0100 | 3 | NA18944.hp1 NA18971.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-6-1981T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778159 | ||||||
chr12:50778224
|
C | CT | 204 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(201): Show | 210 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-6-1896dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778224 | |||||
chr12:50778224
|
C | CTT | 21 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(18): Show | 21 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-1897_-6-1896dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778224 | |||||
chr12:50778224
|
CT | C | 31 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(28): Show | 33 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6-1896delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778224 | |||||
chr12:50778350
|
T | C | 65 | a0001c0002t0002g0012a0001c0002t0002g0018a0001c0002t0002g0095others(62): Show | 66 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.-6-1790T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778350 | ||||||
chr12:50778385
|
C | T | 2 | a0001c0001t0003g0041a0001c0001t0003g0067 | 2 | NA19003.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-6-1755C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778385 | ||||||
chr12:50778467
|
C | T | 1 | a0001c0003t0004g0309 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-6-1673C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778467 | ||||||
chr12:50778560
|
A | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-6-1580A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778560 | ||||||
chr12:50778595
|
ACTT | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0002g0002others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-1544_-6-1542del others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778595 | ||||||
chr12:50778596
|
C | CT | 16 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0212others(13): Show | 18 | HG00733.hp1 HG00735.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-6-1531dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50778596 | |||||
chr12:50778697
|
C | T | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-6-1443C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778697 | ||||||
chr12:50778780
|
A | G | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-1360A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778780 | ||||||
chr12:50778824
|
G | A | 5 | a0001c0002t0002g0184a0001c0002t0002g0185a0001c0002t0002g0186others(2): Show | 5 | HG02132.hp2 NA18959.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-1316G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778824 | ||||||
chr12:50778915
|
C | G | 1 | a0001c0001t0001g0324 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-6-1225C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778915 | ||||||
chr12:50778956
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-6-1184C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50778956 | ||||||
chr12:50779156
|
C | A | 1 | a0001c0001t0001g0355 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-6-984C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779156 | ||||||
chr12:50779166
|
T | C | 1 | a0001c0001t0005g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-6-974T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779166 | ||||||
chr12:50779207
|
A | G | 1 | a0001c0001t0005g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-933A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779207 | ||||||
chr12:50779409
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-6-731C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779409 | ||||||
chr12:50779419
|
G | T | 1 | a0001c0002t0002g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-6-721G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779419 | ||||||
chr12:50779550
|
C | CT | 7 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0003g0076others(4): Show | 7 | HG01358.hp1 HG03486.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-576dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50779550 | |||||
chr12:50779550
|
C | G | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-590C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779550 | ||||||
chr12:50779550
|
CT | C | 24 | a0001c0001t0001g0310a0001c0001t0003g0041a0001c0002t0001g0299others(21): Show | 24 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-6-576delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr12 | 50779550 | |||||
chr12:50779621
|
T | C | 1 | a0001c0002t0002g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-6-519T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779621 | ||||||
chr12:50779695
|
A | G | 1 | a0001c0002t0006g0295 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-6-445A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779695 | ||||||
chr12:50779950
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-6-190A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 1/6 | chr12 | 50779950 | ||||||
chr12:50780347
|
T | C | 1 | a0001c0001t0015g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.93+109T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780347 | ||||||
chr12:50780413
|
C | T | 2 | a0001c0002t0002g0002a0001c0002t0002g0021 | 4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+175C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780413 | ||||||
chr12:50780446
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.93+208A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780446 | ||||||
chr12:50780486
|
A | G | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+248A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780486 | ||||||
chr12:50780507
|
G | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+269G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780507 | ||||||
chr12:50780577
|
G | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.93+339G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780577 | ||||||
chr12:50780650
|
GT | G | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+414delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50780650 | |||||
chr12:50780652
|
T | TA | 28 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(25): Show | 29 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.93+429dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50780652 | |||||
chr12:50780652
|
TA | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(216): Show | 227 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.93+429delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50780652 | |||||
chr12:50780663
|
A | C | 1 | a0001c0001t0005g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.93+425A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780663 | ||||||
chr12:50780763
|
C | A | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18955.hp2 NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.93+525C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780763 | ||||||
chr12:50780775
|
A | G | 7 | a0001c0002t0004g0305a0001c0002t0006g0295a0001c0002t0006g0301others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+537A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780775 | ||||||
chr12:50780781
|
C | T | 4 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(1): Show | 4 | HG02559.hp2 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+543C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780781 | ||||||
chr12:50780815
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.93+577C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780815 | ||||||
chr12:50780874
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0259a0001c0001t0001g0274others(3): Show | 7 | HG00408.hp1 HG00621.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+636C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780874 | ||||||
chr12:50780946
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+708C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50780946 | ||||||
chr12:50781260
|
A | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+1022A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781260 | ||||||
chr12:50781313
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0310others(2): Show | 6 | HG01167.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+1075C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781313 | ||||||
chr12:50781335
|
A | G | 1 | a0001c0001t0015g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.93+1097A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781335 | ||||||
chr12:50781341
|
T | C | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+1103T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781341 | ||||||
chr12:50781380
|
C | T | 1 | a0002c0005t0001g0333 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.93+1142C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781380 | ||||||
chr12:50781482
|
G | A | 1 | a0001c0001t0004g0346 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.93+1244G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781482 | ||||||
chr12:50781490
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(8): Show | 13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+1252G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781490 | ||||||
chr12:50781595
|
C | T | 1 | a0001c0001t0001g0355 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.93+1357C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781595 | ||||||
chr12:50781907
|
C | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(209): Show | 218 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.93+1669C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50781907 | ||||||
chr12:50781915
|
C | CA | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+1696dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50781915 | |||||
chr12:50781915
|
CA | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(262): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.93+1696delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50781915 | |||||
chr12:50782001
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.93+1763C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782001 | ||||||
chr12:50782169
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.93+1931A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782169 | ||||||
chr12:50782234
|
G | GT | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0002g0002others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+2004dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782234 | |||||
chr12:50782241
|
TTG | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2005_93+2006del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782241 | |||||
chr12:50782255
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.93+2017A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782255 | ||||||
chr12:50782255
|
ATTTG | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2029_93+2032del others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782255 | |||||
chr12:50782279
|
A | C | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93+2041A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782279 | ||||||
chr12:50782318
|
C | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93+2080C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782318 | ||||||
chr12:50782324
|
C | T | 1 | a0001c0001t0003g0092 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.93+2086C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782324 | ||||||
chr12:50782345
|
T | TCCCCCCA others(27): Show |
1 | a0001c0001t0003g0041 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.93+2107_93+2108ins others(34): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782345 | ||||||
chr12:50782346
|
T | C | 1 | a0001c0001t0003g0041 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.93+2108T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782346 | ||||||
chr12:50782380
|
C | T | 7 | a0001c0002t0004g0305a0001c0002t0006g0295a0001c0002t0006g0301others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+2142C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782380 | ||||||
chr12:50782416
|
C | T | 5 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+2178C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782416 | ||||||
chr12:50782490
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+2252C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782490 | ||||||
chr12:50782551
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2313G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782551 | ||||||
chr12:50782554
|
C | CT | 66 | a0001c0001t0001g0016a0001c0001t0001g0210a0001c0001t0001g0235others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.93+2336dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782554 | |||||
chr12:50782554
|
CTT | C | 6 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.93+2335_93+2336del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782554 | |||||
chr12:50782581
|
G | A | 3 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.93+2343G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782581 | ||||||
chr12:50782687
|
C | CT | 74 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0210others(71): Show | 76 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.93+2469dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782687 | |||||
chr12:50782687
|
CT | C | 8 | a0001c0001t0001g0317a0001c0002t0002g0018a0001c0002t0002g0105others(5): Show | 8 | HG02155.hp1 HG02976.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+2469delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782687 | |||||
chr12:50782687
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0002g0159a0001c0007t0002g0319 | 2 | HG00140.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.93+2459_93+2469del others(11): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50782687 | |||||
chr12:50782753
|
G | T | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+2515G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782753 | ||||||
chr12:50782808
|
C | T | 10 | a0001c0002t0001g0325a0001c0002t0001g0328a0001c0002t0001g0329others(7): Show | 10 | HG01071.hp1 HG02109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.93+2570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782808 | ||||||
chr12:50782890
|
A | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.93+2652A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782890 | ||||||
chr12:50782892
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0311 | 3 | HG01167.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.93+2654A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782892 | ||||||
chr12:50782921
|
G | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.93+2683G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782921 | ||||||
chr12:50782945
|
C | T | 1 | a0001c0002t0013g0303 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.93+2707C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782945 | ||||||
chr12:50782981
|
C | T | 4 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0070others(1): Show | 4 | HG00673.hp1 HG01358.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+2743C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50782981 | ||||||
chr12:50783043
|
A | T | 1 | a0001c0001t0001g0335 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.93+2805A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783043 | ||||||
chr12:50783055
|
TTC | T | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.93+2822_93+2823del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50783055 | |||||
chr12:50783176
|
G | A | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93+2938G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783176 | ||||||
chr12:50783764
|
A | T | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.93+3526A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783764 | ||||||
chr12:50783845
|
C | T | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG00642.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+3607C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783845 | ||||||
chr12:50783865
|
T | TA | 33 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(30): Show | 35 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.93+3627_93+3628ins others(1): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783865 | ||||||
chr12:50783866
|
G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(32): Show | 37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+3628G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50783866 | ||||||
chr12:50783866
|
GA | G | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0003g0007others(79): Show | 86 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.93+3646delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50783866 | |||||
chr12:50783866
|
GAA | G | 46 | a0001c0001t0001g0118a0001c0002t0002g0032a0001c0002t0002g0096others(43): Show | 46 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.93+3645_93+3646del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50783866 | |||||
chr12:50784121
|
C | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0258a0001c0001t0001g0268others(4): Show | 7 | HG00733.hp2 HG01081.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+3883C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784121 | ||||||
chr12:50784782
|
TA | T | 3 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298 | 3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.93+4545delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784782 | ||||||
chr12:50784877
|
T | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0310a0001c0001t0001g0311others(1): Show | 5 | HG01167.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+4639T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784877 | ||||||
chr12:50784934
|
A | T | 1 | a0001c0001t0003g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.93+4696A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50784934 | ||||||
chr12:50785046
|
C | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0316 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.93+4808C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785046 | ||||||
chr12:50785095
|
C | T | 1 | a0001c0002t0001g0331 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.93+4857C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785095 | ||||||
chr12:50785123
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0267a0001c0001t0001g0281 | 3 | HG00642.hp2 HG00738.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.93+4885A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785123 | ||||||
chr12:50785280
|
TACATACA others(3): Show |
T | 1 | a0001c0002t0002g0002 | 3 | HG02258.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.93+5046_93+5055del others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785280 | |||||
chr12:50785280
|
TACATACA others(7): Show |
T | 1 | a0001c0002t0002g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.93+5046_93+5059del others(14): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785280 | |||||
chr12:50785284
|
TAC | T | 3 | a0001c0001t0003g0053a0001c0002t0002g0151a0001c0002t0002g0153 | 3 | HG01884.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.93+5100_93+5101del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACAC | T | 18 | a0001c0001t0001g0312a0001c0002t0002g0096a0001c0002t0002g0101others(15): Show | 18 | HG00140.hp2 HG00544.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.93+5098_93+5101del others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACAC | T | 43 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0310others(40): Show | 45 | HG00438.hp1 HG01081.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.93+5096_93+5101del others(6): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(1): Show |
T | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0213others(45): Show | 49 | HG00597.hp1 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.93+5094_93+5101del others(8): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(3): Show |
T | 59 | a0001c0001t0001g0118a0001c0001t0001g0211a0001c0001t0001g0214others(56): Show | 62 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.93+5092_93+5101del others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(5): Show |
T | 90 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(87): Show | 97 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.93+5090_93+5101del others(12): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(7): Show |
T | 31 | a0001c0001t0001g0015a0001c0001t0001g0210a0001c0001t0001g0218others(28): Show | 32 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.93+5088_93+5101del others(14): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(9): Show |
T | 35 | a0001c0001t0001g0239a0001c0001t0001g0257a0001c0001t0001g0266others(32): Show | 37 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+5086_93+5101del others(16): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(11): Show |
T | 3 | a0001c0001t0001g0343a0001c0001t0005g0036a0001c0002t0004g0305 | 3 | HG01109.hp1 HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.93+5084_93+5101del others(18): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(15): Show |
T | 7 | a0001c0002t0002g0139a0001c0002t0002g0183a0001c0002t0002g0201others(4): Show | 7 | HG02486.hp1 HG03225.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+5080_93+5101del others(22): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785284
|
TACACACA others(17): Show |
T | 20 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(17): Show | 20 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.93+5078_93+5101del others(24): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785284 | |||||
chr12:50785343
|
G | A | 1 | a0001c0002t0002g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93+5105G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785343 | ||||||
chr12:50785417
|
G | A | 1 | a0001c0003t0004g0358 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.93+5179G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785417 | ||||||
chr12:50785557
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.93+5319G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785557 | ||||||
chr12:50785742
|
T | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.93+5504T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785742 | ||||||
chr12:50785808
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.93+5570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50785808 | ||||||
chr12:50785906
|
AATGACAT others(21): Show |
A | 3 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298 | 3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.93+5681_93+5708del others(28): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50785906 | |||||
chr12:50786093
|
T | C | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+5855T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786093 | ||||||
chr12:50786097
|
C | T | 1 | a0001c0002t0002g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.93+5859C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786097 | ||||||
chr12:50786360
|
C | T | 117 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0001t0015g0163others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.93+6122C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786360 | ||||||
chr12:50786428
|
TGGG | T | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.93+6191_93+6193del others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786428 | ||||||
chr12:50786564
|
C | A | 1 | a0001c0001t0001g0355 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.93+6326C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786564 | ||||||
chr12:50786690
|
C | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0061 | 3 | HG02886.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.93+6452C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786690 | ||||||
chr12:50786967
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.93+6729G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50786967 | ||||||
chr12:50787094
|
G | T | 2 | a0001c0001t0004g0349a0001c0001t0004g0356 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.93+6856G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787094 | ||||||
chr12:50787165
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.93+6927T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787165 | ||||||
chr12:50787498
|
C | T | 1 | a0001c0001t0005g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.93+7260C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787498 | ||||||
chr12:50787916
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(243): Show | 254 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.93+7678T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787916 | ||||||
chr12:50787918
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.93+7680A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50787918 | ||||||
chr12:50788187
|
C | CT | 15 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0001g0330others(12): Show | 17 | HG00140.hp2 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-7709dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50788187 | |||||
chr12:50788232
|
G | A | 1 | a0001c0002t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.94-7677G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788232 | ||||||
chr12:50788321
|
C | T | 1 | a0001c0002t0002g0203 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.94-7588C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788321 | ||||||
chr12:50788326
|
G | T | 7 | a0001c0002t0004g0305a0001c0002t0006g0295a0001c0002t0006g0301others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-7583G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788326 | ||||||
chr12:50788339
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(230): Show | 239 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.94-7570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788339 | ||||||
chr12:50788398
|
C | T | 1 | a0001c0002t0001g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.94-7511C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788398 | ||||||
chr12:50788587
|
A | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-7322A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788587 | ||||||
chr12:50788629
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(231): Show | 240 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.94-7280A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788629 | ||||||
chr12:50788700
|
C | T | 1 | a0001c0002t0002g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.94-7209C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50788700 | ||||||
chr12:50789086
|
T | G | 1 | a0001c0002t0002g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.94-6823T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789086 | ||||||
chr12:50789099
|
G | GACAGAGT others(11): Show |
1 | a0001c0002t0002g0183 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.94-6809_94-6792dup others(18): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50789099 | |||||
chr12:50789229
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94-6680C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789229 | ||||||
chr12:50789290
|
A | G | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-6619A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789290 | ||||||
chr12:50789528
|
C | T | 117 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0001t0015g0163others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.94-6381C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789528 | ||||||
chr12:50789648
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.94-6261G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789648 | ||||||
chr12:50789852
|
G | T | 1 | a0001c0002t0002g0187 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.94-6057G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50789852 | ||||||
chr12:50790197
|
A | AT | 226 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(223): Show | 233 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.94-5692dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50790197 | |||||
chr12:50790197
|
A | ATT | 15 | a0001c0001t0001g0219a0001c0001t0001g0234a0001c0001t0001g0238others(12): Show | 16 | HG01071.hp2 HG01123.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.94-5693_94-5692dup others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50790197 | |||||
chr12:50790265
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0002g0002others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-5644C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790265 | ||||||
chr12:50790309
|
A | G | 5 | a0001c0001t0003g0007a0001c0001t0003g0061a0001c0002t0006g0301others(2): Show | 6 | HG02109.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-5600A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790309 | ||||||
chr12:50790472
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(283): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.94-5437T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790472 | ||||||
chr12:50790794
|
A | G | 117 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0001t0015g0163others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.94-5115A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790794 | ||||||
chr12:50790846
|
G | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0310others(2): Show | 6 | HG01167.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-5063G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790846 | ||||||
chr12:50790976
|
AC | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.94-4932delC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50790976 | ||||||
chr12:50791081
|
G | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.94-4828G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791081 | ||||||
chr12:50791248
|
C | T | 1 | a0001c0002t0002g0186 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94-4661C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791248 | ||||||
chr12:50791335
|
C | T | 1 | a0001c0001t0003g0078 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.94-4574C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791335 | ||||||
chr12:50791552
|
C | CA | 12 | a0001c0001t0001g0020a0001c0001t0001g0271a0001c0001t0001g0317others(9): Show | 12 | HG01074.hp1 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.94-4344dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50791552 | |||||
chr12:50791819
|
T | C | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.94-4090T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791819 | ||||||
chr12:50791924
|
A | T | 2 | a0001c0001t0009g0164a0001c0001t0009g0165 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.94-3985A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791924 | ||||||
chr12:50791981
|
C | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.94-3928C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50791981 | ||||||
chr12:50792015
|
G | A | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-3894G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792015 | ||||||
chr12:50792167
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.94-3742C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792167 | ||||||
chr12:50792215
|
G | A | 1 | a0001c0002t0002g0194 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94-3694G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792215 | ||||||
chr12:50792239
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.94-3670T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50792239 | ||||||
chr12:50792610
|
A | AT | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.94-3298dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50792610 | |||||
chr12:50792768
|
CT | C | 9 | a0001c0002t0002g0095a0001c0002t0002g0172a0001c0002t0002g0173others(6): Show | 9 | HG01081.hp2 HG02132.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.94-3130delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50792768 | |||||
chr12:50793450
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94-2459C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793450 | ||||||
chr12:50793507
|
C | T | 117 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0001t0015g0163others(114): Show | 118 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.94-2402C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793507 | ||||||
chr12:50793547
|
C | T | 3 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG02559.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.94-2362C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793547 | ||||||
chr12:50793612
|
G | A | 1 | a0001c0001t0003g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94-2297G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793612 | ||||||
chr12:50793633
|
CA | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(269): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.94-2258delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793633 | |||||
chr12:50793633
|
CAA | C | 7 | a0001c0001t0001g0215a0001c0001t0001g0245a0001c0001t0001g0321others(4): Show | 7 | HG02897.hp2 HG04115.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-2259_94-2258del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793633 | |||||
chr12:50793691
|
T | TTAAA | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.94-2215_94-2214ins others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793691 | |||||
chr12:50793701
|
G | GTTA | 286 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(283): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.94-2205_94-2203dup others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr12 | 50793701 | |||||
chr12:50793973
|
G | A | 7 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.94-1936G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50793973 | ||||||
chr12:50794096
|
G | A | 1 | a0001c0002t0002g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.94-1813G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794096 | ||||||
chr12:50794111
|
C | T | 1 | a0001c0002t0014g0327 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.94-1798C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794111 | ||||||
chr12:50794183
|
C | T | 7 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(4): Show | 7 | HG02630.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-1726C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794183 | ||||||
chr12:50794227
|
G | A | 1 | a0001c0001t0004g0351 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.94-1682G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794227 | ||||||
chr12:50794229
|
C | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-1680C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794229 | ||||||
chr12:50794230
|
G | A | 2 | a0001c0001t0003g0058a0001c0001t0003g0071 | 2 | NA19007.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.94-1679G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794230 | ||||||
chr12:50794373
|
T | C | 1 | a0001c0002t0002g0095 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.94-1536T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794373 | ||||||
chr12:50794436
|
G | C | 1 | a0001c0001t0001g0293 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.94-1473G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794436 | ||||||
chr12:50794551
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(243): Show | 254 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.94-1358T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794551 | ||||||
chr12:50794591
|
G | A | 1 | a0001c0002t0002g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.94-1318G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794591 | ||||||
chr12:50794614
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(231): Show | 240 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.94-1295C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794614 | ||||||
chr12:50794731
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.94-1178G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794731 | ||||||
chr12:50794743
|
G | T | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.94-1166G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794743 | ||||||
chr12:50794855
|
G | A | 29 | a0001c0001t0001g0308a0001c0001t0001g0335a0001c0001t0001g0336others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.94-1054G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794855 | ||||||
chr12:50794877
|
C | T | 5 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-1032C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794877 | ||||||
chr12:50794944
|
A | T | 1 | a0001c0001t0001g0311 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94-965A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50794944 | ||||||
chr12:50795210
|
G | C | 2 | a0001c0002t0002g0139a0001c0002t0002g0160 | 2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.94-699G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795210 | ||||||
chr12:50795375
|
A | G | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-534A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795375 | ||||||
chr12:50795461
|
T | A | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94-448T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795461 | ||||||
chr12:50795584
|
T | C | 5 | a0001c0002t0002g0032a0001c0002t0002g0101a0001c0002t0002g0102others(2): Show | 5 | NA18950.hp2 NA18953.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-325T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795584 | ||||||
chr12:50795718
|
A | T | 1 | a0001c0002t0002g0183 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.94-191A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795718 | ||||||
chr12:50795836
|
T | C | 50 | a0001c0001t0001g0118a0001c0002t0002g0032a0001c0002t0002g0096others(47): Show | 50 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.94-73T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 2/6 | chr12 | 50795836 | ||||||
chr12:50796054
|
A | C | 1 | a0001c0002t0002g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.194+45A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796054 | ||||||
chr12:50796101
|
C | T | 1 | a0001c0002t0002g0167 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.194+92C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796101 | ||||||
chr12:50796102
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.194+93G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796102 | ||||||
chr12:50796139
|
T | A | 1 | a0001c0002t0002g0183 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.194+130T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796139 | ||||||
chr12:50796164
|
G | A | 1 | a0001c0001t0003g0042 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.194+155G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796164 | ||||||
chr12:50796185
|
A | G | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.194+176A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796185 | ||||||
chr12:50796298
|
G | A | 2 | a0001c0001t0004g0339a0001c0001t0004g0340 | 2 | HG00140.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.194+289G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796298 | ||||||
chr12:50796307
|
T | C | 1 | a0001c0002t0002g0117 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.194+298T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796307 | ||||||
chr12:50796355
|
C | T | 6 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+346C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796355 | ||||||
chr12:50796649
|
C | T | 5 | a0001c0002t0002g0112a0001c0002t0002g0122a0001c0002t0002g0140others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+640C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796649 | ||||||
chr12:50796700
|
CA | C | 7 | a0001c0001t0001g0232a0001c0001t0001g0247a0001c0001t0001g0270others(4): Show | 7 | HG01993.hp1 HG02630.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+706delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50796700 | |||||
chr12:50796823
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.194+814C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796823 | ||||||
chr12:50796909
|
C | T | 29 | a0001c0001t0001g0308a0001c0001t0001g0335a0001c0001t0001g0336others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.194+900C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796909 | ||||||
chr12:50796928
|
G | A | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.194+919G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796928 | ||||||
chr12:50796978
|
G | A | 1 | a0001c0002t0002g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.194+969G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50796978 | ||||||
chr12:50797366
|
A | C | 1 | a0001c0001t0003g0053 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.194+1357A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797366 | ||||||
chr12:50797387
|
A | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.194+1378A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797387 | ||||||
chr12:50797510
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.194+1501A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797510 | ||||||
chr12:50797647
|
T | A | 1 | a0001c0002t0002g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.194+1638T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797647 | ||||||
chr12:50797741
|
T | G | 34 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(31): Show | 36 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.194+1732T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797741 | ||||||
chr12:50797916
|
G | C | 1 | a0001c0002t0002g0098 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.194+1907G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797916 | ||||||
chr12:50797944
|
G | A | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.194+1935G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797944 | ||||||
chr12:50797998
|
A | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(283): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.194+1989A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50797998 | ||||||
chr12:50798023
|
A | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(360): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.194+2014A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798023 | ||||||
chr12:50798319
|
T | G | 1 | a0001c0002t0002g0184 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.194+2310T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798319 | ||||||
chr12:50798453
|
C | T | 1 | a0001c0002t0001g0329 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.194+2444C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798453 | ||||||
chr12:50798544
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.194+2535C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798544 | ||||||
chr12:50798675
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.194+2666C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50798675 | ||||||
chr12:50799037
|
A | C | 1 | a0001c0002t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+3028A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799037 | ||||||
chr12:50799092
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0253 | 2 | HG02056.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.194+3083A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799092 | ||||||
chr12:50799230
|
C | G | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.194+3221C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799230 | ||||||
chr12:50799301
|
C | A | 1 | a0001c0001t0003g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.194+3292C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799301 | ||||||
chr12:50799344
|
C | T | 6 | a0001c0002t0002g0143a0001c0002t0002g0144a0001c0002t0002g0145others(3): Show | 6 | HG02280.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+3335C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799344 | ||||||
chr12:50799412
|
T | C | 1 | a0001c0002t0002g0185 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.194+3403T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799412 | ||||||
chr12:50799494
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.194+3485C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799494 | ||||||
chr12:50799654
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(8): Show | 13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.194+3645G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799654 | ||||||
chr12:50799680
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0316 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.194+3671A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799680 | ||||||
chr12:50799862
|
G | A | 1 | a0001c0002t0002g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.194+3853G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50799862 | ||||||
chr12:50800027
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.194+4018T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800027 | ||||||
chr12:50800177
|
A | C | 1 | a0001c0002t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+4168A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800177 | ||||||
chr12:50800222
|
A | G | 3 | a0001c0001t0004g0017a0001c0001t0004g0338a0001c0001t0004g0342 | 4 | HG00639.hp2 HG00741.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+4213A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800222 | ||||||
chr12:50800380
|
G | A | 2 | a0001c0002t0002g0113a0001c0002t0002g0114 | 2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.194+4371G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800380 | ||||||
chr12:50800472
|
G | T | 1 | a0001c0002t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+4463G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800472 | ||||||
chr12:50800473
|
T | C | 1 | a0001c0002t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.194+4464T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800473 | ||||||
chr12:50800578
|
C | G | 1 | a0001c0002t0002g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.194+4569C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800578 | ||||||
chr12:50800647
|
G | A | 3 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298 | 3 | HG02486.hp1 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.194+4638G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800647 | ||||||
chr12:50800700
|
G | C | 1 | a0001c0002t0006g0304 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.194+4691G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800700 | ||||||
chr12:50800721
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0002g0002others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+4712A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800721 | ||||||
chr12:50800810
|
T | C | 1 | a0001c0002t0002g0124 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.194+4801T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800810 | ||||||
chr12:50800823
|
G | C | 1 | a0001c0002t0002g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.194+4814G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800823 | ||||||
chr12:50800926
|
C | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.194+4917C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50800926 | ||||||
chr12:50801016
|
A | G | 74 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(71): Show | 78 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.194+5007A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801016 | ||||||
chr12:50801044
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(209): Show | 218 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.194+5035G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801044 | ||||||
chr12:50801081
|
C | T | 30 | a0001c0001t0001g0308a0001c0001t0001g0335a0001c0001t0001g0336others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.194+5072C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801081 | ||||||
chr12:50801319
|
T | TA | 7 | a0001c0001t0001g0221a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG02056.hp2 HG02071.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+5319dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50801319 | |||||
chr12:50801423
|
A | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.194+5414A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801423 | ||||||
chr12:50801575
|
A | G | 1 | a0001c0002t0002g0197 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.194+5566A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801575 | ||||||
chr12:50801677
|
A | G | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194+5668A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801677 | ||||||
chr12:50801738
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.194+5729C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801738 | ||||||
chr12:50801885
|
CCT | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0310others(2): Show | 6 | HG01167.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.194+5880_194+5881d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50801885 | |||||
chr12:50801965
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(283): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.194+5956G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50801965 | ||||||
chr12:50802039
|
A | G | 1 | a0001c0002t0006g0304 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.194+6030A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802039 | ||||||
chr12:50802167
|
G | A | 2 | a0001c0002t0004g0305a0001c0002t0006g0306 | 2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.194+6158G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802167 | ||||||
chr12:50802179
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.194+6170A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802179 | ||||||
chr12:50802291
|
C | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194+6282C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802291 | ||||||
chr12:50802397
|
C | T | 2 | a0001c0001t0003g0022a0001c0001t0003g0046 | 2 | HG02129.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.194+6388C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802397 | ||||||
chr12:50802503
|
T | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG00642.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+6494T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802503 | ||||||
chr12:50802536
|
C | T | 1 | a0001c0002t0002g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.194+6527C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802536 | ||||||
chr12:50802765
|
G | A | 8 | a0001c0002t0002g0018a0001c0002t0002g0105a0001c0002t0002g0106others(5): Show | 8 | HG02056.hp1 HG02155.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.195-6691G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802765 | ||||||
chr12:50802814
|
G | A | 2 | a0001c0002t0002g0002a0001c0002t0002g0021 | 4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-6642G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802814 | ||||||
chr12:50802861
|
G | C | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-6595G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802861 | ||||||
chr12:50802871
|
C | CA | 157 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(154): Show | 163 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.195-6562dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | |||||
chr12:50802871
|
C | CAA | 96 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0210others(93): Show | 100 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.195-6563_195-6562d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | |||||
chr12:50802871
|
C | CAAA | 11 | a0001c0002t0002g0126a0001c0002t0002g0168a0001c0002t0002g0179others(8): Show | 11 | HG00099.hp2 HG01175.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.195-6564_195-6562d others(5): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | |||||
chr12:50802871
|
C | CAAAA | 18 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(15): Show | 18 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.195-6565_195-6562d others(6): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | |||||
chr12:50802871
|
CA | C | 6 | a0001c0001t0003g0007a0001c0001t0003g0044a0001c0001t0003g0057others(3): Show | 7 | HG02523.hp2 HG02886.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.195-6562delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50802871 | |||||
chr12:50802954
|
C | G | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-6502C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802954 | ||||||
chr12:50802967
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.195-6489G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50802967 | ||||||
chr12:50803099
|
A | T | 6 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-6357A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803099 | ||||||
chr12:50803184
|
G | T | 1 | a0001c0004t0002g0199 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.195-6272G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803184 | ||||||
chr12:50803249
|
CAA | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 98 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.195-6206_195-6205d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803249 | ||||||
chr12:50803268
|
C | CA | 118 | a0001c0001t0001g0118a0001c0001t0009g0164a0001c0001t0009g0165others(115): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.195-6176dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50803268 | |||||
chr12:50803498
|
TA | T | 110 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0118others(107): Show | 113 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.195-5943delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50803498 | |||||
chr12:50803498
|
TAA | T | 21 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0324others(18): Show | 21 | HG02056.hp1 HG02155.hp1 HG02976.hp1 others(18): Show |
intron_variant | MODIFIER | c.195-5944_195-5943d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50803498 | |||||
chr12:50803793
|
A | C | 15 | a0001c0002t0002g0018a0001c0002t0002g0105a0001c0002t0002g0106others(12): Show | 15 | HG02056.hp1 HG02155.hp1 HG03492.hp2 others(12): Show |
intron_variant | MODIFIER | c.195-5663A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803793 | ||||||
chr12:50803839
|
C | T | 1 | a0001c0002t0002g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.195-5617C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803839 | ||||||
chr12:50803886
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.195-5570C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803886 | ||||||
chr12:50803934
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.195-5522C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50803934 | ||||||
chr12:50804011
|
A | C | 34 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(31): Show | 36 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-5445A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804011 | ||||||
chr12:50804052
|
T | G | 1 | a0001c0001t0001g0235 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.195-5404T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804052 | ||||||
chr12:50804238
|
A | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(9): Show | 14 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.195-5218A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804238 | ||||||
chr12:50804355
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0002t0002g0002others(1): Show | 6 | HG02257.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-5101A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804355 | ||||||
chr12:50804659
|
C | T | 2 | a0001c0002t0001g0329a0002c0005t0001g0333 | 2 | HG01071.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.195-4797C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804659 | ||||||
chr12:50804810
|
C | CT | 11 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0287others(8): Show | 11 | HG00673.hp1 HG01981.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.195-4630dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50804810 | |||||
chr12:50804810
|
CT | C | 11 | a0001c0001t0001g0286a0001c0001t0004g0349a0001c0002t0002g0207others(8): Show | 11 | HG01168.hp1 HG01943.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-4630delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50804810 | |||||
chr12:50804826
|
T | C | 2 | a0001c0002t0002g0167a0001c0002t0002g0184 | 2 | HG04204.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.195-4630T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804826 | ||||||
chr12:50804834
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.195-4622C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804834 | ||||||
chr12:50804835
|
G | A | 4 | a0001c0001t0001g0313a0001c0001t0003g0053a0001c0001t0003g0361others(1): Show | 4 | HG02886.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-4621G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50804835 | ||||||
chr12:50805062
|
C | T | 1 | a0001c0001t0015g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195-4394C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805062 | ||||||
chr12:50805231
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-4225C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805231 | ||||||
chr12:50805483
|
G | C | 1 | a0001c0001t0003g0087 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.195-3973G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805483 | ||||||
chr12:50805538
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.195-3918A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805538 | ||||||
chr12:50805561
|
C | CA | 51 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(48): Show | 54 | HG01071.hp1 HG01106.hp1 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.195-3874dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50805561 | |||||
chr12:50805561
|
CA | C | 10 | a0001c0001t0001g0219a0001c0001t0003g0041a0001c0001t0003g0043others(7): Show | 10 | HG01517.hp1 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-3874delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50805561 | |||||
chr12:50805572
|
A | C | 1 | a0001c0002t0002g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.195-3884A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805572 | ||||||
chr12:50805601
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(8): Show | 13 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.195-3855C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805601 | ||||||
chr12:50805860
|
A | C | 1 | a0001c0001t0003g0084 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.195-3596A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805860 | ||||||
chr12:50805940
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 99 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.195-3516C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805940 | ||||||
chr12:50805968
|
T | C | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.195-3488T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50805968 | ||||||
chr12:50806100
|
G | A | 1 | a0001c0002t0002g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.195-3356G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50806100 | ||||||
chr12:50806152
|
G | GA | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0234others(6): Show | 11 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-3290dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50806152 | |||||
chr12:50806152
|
GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0001g0226 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.195-3299_195-3290d others(12): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50806152 | |||||
chr12:50806460
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0231a0001c0001t0001g0259others(6): Show | 10 | HG00408.hp1 HG00621.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-2996C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50806460 | ||||||
chr12:50806695
|
G | GA | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0118others(16): Show | 21 | HG00609.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.195-2748dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50806695 | |||||
chr12:50807308
|
G | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(6): Show | 11 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.195-2148G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807308 | ||||||
chr12:50807362
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.195-2094C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807362 | ||||||
chr12:50807367
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-2089G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807367 | ||||||
chr12:50807387
|
G | T | 1 | a0001c0001t0003g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.195-2069G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807387 | ||||||
chr12:50807548
|
A | T | 1 | a0001c0002t0002g0032 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.195-1908A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807548 | ||||||
chr12:50807655
|
T | TC | 2 | a0001c0001t0001g0013a0001c0001t0001g0212 | 3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.195-1801_195-1800i others(3): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807655 | ||||||
chr12:50807656
|
A | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(281): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.195-1800A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807656 | ||||||
chr12:50807656
|
A | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0212 | 3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.195-1800A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807656 | ||||||
chr12:50807802
|
GT | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(137): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.195-1644delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50807802 | |||||
chr12:50807803
|
T | G | 4 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0355others(1): Show | 4 | HG02280.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-1653T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807803 | ||||||
chr12:50807804
|
T | G | 29 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(26): Show | 31 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.195-1652T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807804 | ||||||
chr12:50807811
|
T | G | 1 | a0001c0001t0001g0337 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.195-1645T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807811 | ||||||
chr12:50807811
|
TTG | T | 124 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0246others(121): Show | 127 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.195-1643_195-1642d others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50807811 | |||||
chr12:50807812
|
T | G | 11 | a0001c0001t0001g0249a0001c0001t0001g0313a0001c0001t0001g0314others(8): Show | 11 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-1644T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807812 | ||||||
chr12:50807813
|
G | T | 12 | a0001c0001t0001g0249a0001c0001t0001g0313a0001c0001t0001g0314others(9): Show | 12 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.195-1643G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807813 | ||||||
chr12:50807814
|
T | G | 124 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0246others(121): Show | 127 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.195-1642T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807814 | ||||||
chr12:50807818
|
T | G | 1 | a0002c0005t0001g0333 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.195-1638T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807818 | ||||||
chr12:50807824
|
T | G | 128 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(125): Show | 131 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.195-1632T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807824 | ||||||
chr12:50807900
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.195-1556C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807900 | ||||||
chr12:50807902
|
C | T | 23 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(20): Show | 23 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.195-1554C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807902 | ||||||
chr12:50807966
|
T | C | 127 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(124): Show | 130 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.195-1490T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807966 | ||||||
chr12:50807975
|
A | G | 120 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0009g0164others(117): Show | 123 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.195-1481A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50807975 | ||||||
chr12:50808126
|
A | T | 1 | a0001c0002t0002g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.195-1330A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808126 | ||||||
chr12:50808130
|
T | C | 1 | a0001c0002t0013g0303 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.195-1326T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808130 | ||||||
chr12:50808263
|
C | T | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-1193C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808263 | ||||||
chr12:50808270
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.195-1186C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808270 | ||||||
chr12:50808286
|
T | G | 1 | a0001c0001t0005g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.195-1170T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808286 | ||||||
chr12:50808321
|
T | G | 1 | a0001c0002t0011g0209 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.195-1135T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808321 | ||||||
chr12:50808323
|
T | G | 4 | a0001c0001t0003g0086a0001c0001t0009g0164a0001c0001t0009g0165others(1): Show | 4 | HG01261.hp2 HG02145.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.195-1133T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808323 | ||||||
chr12:50808328
|
T | C | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195-1128T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808328 | ||||||
chr12:50808382
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.195-1074A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808382 | ||||||
chr12:50808414
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195-1042C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808414 | ||||||
chr12:50808541
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.195-915C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808541 | ||||||
chr12:50808625
|
A | C | 1 | a0001c0002t0002g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.195-831A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808625 | ||||||
chr12:50808730
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.195-726G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50808730 | ||||||
chr12:50808743
|
AT | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(98): Show | 106 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.195-699delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50808743 | |||||
chr12:50808771
|
ACT | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(38): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.195-682_195-681del others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50808771 | |||||
chr12:50809014
|
A | G | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.195-442A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809014 | ||||||
chr12:50809029
|
T | TGACTGGC others(512): Show |
1 | a0001c0002t0002g0117 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.195-411_195-410ins others(519): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809029 | |||||
chr12:50809079
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 103 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.195-377A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809079 | ||||||
chr12:50809096
|
G | A | 3 | a0001c0002t0002g0151a0001c0002t0002g0152a0001c0002t0002g0153 | 3 | HG01884.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.195-360G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809096 | ||||||
chr12:50809182
|
T | C | 6 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-274T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809182 | ||||||
chr12:50809233
|
G | T | 1 | a0001c0002t0002g0120 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.195-223G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809233 | ||||||
chr12:50809373
|
C | CA | 80 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0003g0003others(77): Show | 88 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.195-61dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809373 | |||||
chr12:50809373
|
C | CAA | 15 | a0001c0001t0003g0046a0001c0001t0003g0093a0001c0001t0005g0033others(12): Show | 15 | HG01891.hp1 HG02055.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.195-62_195-61dupAA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809373 | |||||
chr12:50809373
|
CA | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(88): Show | 96 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.195-61delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809373 | |||||
chr12:50809381
|
A | T | 1 | a0001c0002t0002g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.195-75A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809381 | ||||||
chr12:50809395
|
ATTAT | A | 30 | a0001c0001t0001g0016a0001c0001t0001g0308a0001c0001t0001g0310others(27): Show | 32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.195-58_195-55delAT others(2): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809395 | |||||
chr12:50809399
|
T | A | 3 | a0001c0001t0001g0307a0001c0001t0001g0355a0001c0003t0004g0348 | 3 | HG01256.hp2 HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.195-57T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809399 | ||||||
chr12:50809400
|
T | A | 33 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(30): Show | 35 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.195-56T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | chr12 | 50809400 | ||||||
chr12:50809443
|
GT | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
splice_region_variant&intron_variant | LOW | c.195-5delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr12 | 50809443 | |||||
chr12:50809593
|
T | C | 114 | a0001c0002t0002g0012a0001c0002t0002g0018a0001c0002t0002g0032others(111): Show | 115 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(112): Show |
splice_region_variant&intron_variant | LOW | c.328+4T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50809593 | ||||||
chr12:50809819
|
C | CTGTTT | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.328+258_328+262dup others(5): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50809819 | |||||
chr12:50809819
|
C | CTGTTTTG others(3): Show |
6 | a0001c0001t0001g0257a0001c0001t0001g0260a0001c0001t0001g0261others(3): Show | 6 | HG00438.hp2 HG00609.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+253_328+262dup others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50809819 | |||||
chr12:50809819
|
CTGTTTTG others(3): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.328+253_328+262del others(10): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50809819 | |||||
chr12:50809905
|
C | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.328+316C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50809905 | ||||||
chr12:50809907
|
C | G | 3 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0001t0015g0163 | 3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.328+318C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50809907 | ||||||
chr12:50810164
|
C | T | 12 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(9): Show | 12 | HG01071.hp1 HG02109.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.328+575C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810164 | ||||||
chr12:50810170
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.328+581A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810170 | ||||||
chr12:50810219
|
C | CT | 102 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(99): Show | 107 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.328+646dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50810219 | |||||
chr12:50810366
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.328+777T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810366 | ||||||
chr12:50810394
|
T | C | 1 | a0001c0002t0002g0168 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.328+805T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810394 | ||||||
chr12:50810479
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.328+890C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810479 | ||||||
chr12:50810509
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.328+920C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810509 | ||||||
chr12:50810512
|
C | T | 43 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(40): Show | 45 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.328+923C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810512 | ||||||
chr12:50810677
|
G | A | 7 | a0001c0002t0004g0305a0001c0002t0006g0295a0001c0002t0006g0301others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+1088G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810677 | ||||||
chr12:50810983
|
G | T | 1 | a0001c0001t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.328+1394G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50810983 | ||||||
chr12:50811155
|
T | C | 139 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(136): Show | 142 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.328+1566T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811155 | ||||||
chr12:50811180
|
C | T | 3 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0001t0015g0163 | 3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.328+1591C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811180 | ||||||
chr12:50811232
|
C | T | 1 | a0001c0002t0002g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.328+1643C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811232 | ||||||
chr12:50811283
|
C | T | 24 | a0001c0001t0001g0355a0001c0001t0004g0017a0001c0001t0004g0338others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.328+1694C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811283 | ||||||
chr12:50811284
|
A | T | 24 | a0001c0001t0001g0355a0001c0001t0004g0017a0001c0001t0004g0338others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.328+1695A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811284 | ||||||
chr12:50811523
|
T | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(360): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.328+1934T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811523 | ||||||
chr12:50811526
|
G | A | 1 | a0001c0002t0010g0206 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.328+1937G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811526 | ||||||
chr12:50811630
|
G | GA | 121 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(118): Show | 126 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.328+2060dupA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50811630 | |||||
chr12:50811630
|
GA | G | 6 | a0001c0001t0001g0324a0001c0001t0003g0003a0001c0001t0003g0024others(3): Show | 7 | HG02723.hp2 HG06807.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+2060delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50811630 | |||||
chr12:50811631
|
A | G | 1 | a0001c0001t0004g0349 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.328+2042A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811631 | ||||||
chr12:50811666
|
T | C | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.328+2077T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811666 | ||||||
chr12:50811691
|
G | C | 1 | a0001c0001t0003g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.328+2102G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811691 | ||||||
chr12:50811733
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.328+2144G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811733 | ||||||
chr12:50811733
|
G | C | 4 | a0001c0001t0003g0049a0001c0001t0003g0050a0001c0001t0003g0051others(1): Show | 4 | HG00642.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+2144G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811733 | ||||||
chr12:50811933
|
C | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.329-2077C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811933 | ||||||
chr12:50811980
|
C | T | 117 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0018others(114): Show | 120 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.329-2030C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50811980 | ||||||
chr12:50812160
|
AC | A | 45 | a0001c0002t0002g0012a0001c0002t0002g0095a0001c0002t0002g0126others(42): Show | 46 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.329-1849delC | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50812160 | ||||||
chr12:50812292
|
C | T | 1 | a0001c0002t0002g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-1718C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50812292 | ||||||
chr12:50812912
|
T | A | 1 | a0001c0001t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.329-1098T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50812912 | ||||||
chr12:50813088
|
A | G | 22 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(19): Show | 22 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.329-922A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813088 | ||||||
chr12:50813098
|
G | A | 2 | a0001c0002t0007g0296a0001c0002t0007g0298 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.329-912G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813098 | ||||||
chr12:50813121
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.329-889T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813121 | ||||||
chr12:50813226
|
C | G | 1 | a0001c0002t0002g0166 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.329-784C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813226 | ||||||
chr12:50813411
|
A | G | 1 | a0002c0005t0001g0333 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.329-599A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813411 | ||||||
chr12:50813630
|
A | G | 3 | a0001c0001t0003g0045a0001c0001t0003g0048a0001c0001t0003g0056 | 3 | NA18999.hp1 NA19001.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.329-380A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813630 | ||||||
chr12:50813631
|
T | C | 44 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(41): Show | 46 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.329-379T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813631 | ||||||
chr12:50813820
|
GA | G | 285 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(282): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.329-178delA | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr12 | 50813820 | |||||
chr12:50813853
|
T | C | 1 | a0001c0002t0002g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-157T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813853 | ||||||
chr12:50813881
|
G | C | 3 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0001t0015g0163 | 3 | HG02145.hp2 HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.329-129G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813881 | ||||||
chr12:50813921
|
A | G | 43 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0020others(40): Show | 45 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.329-89A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813921 | ||||||
chr12:50813950
|
C | T | 6 | a0001c0002t0002g0143a0001c0002t0002g0144a0001c0002t0002g0145others(3): Show | 6 | HG02280.hp2 HG02897.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-60C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 4/6 | chr12 | 50813950 | ||||||
chr12:50814456
|
T | A | 2 | a0001c0002t0002g0002a0001c0002t0002g0021 | 4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+17T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814456 | ||||||
chr12:50814692
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.671+253A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814692 | ||||||
chr12:50814815
|
T | G | 1 | a0001c0002t0002g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.671+376T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814815 | ||||||
chr12:50814820
|
C | CT | 29 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337others(26): Show | 30 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+399dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50814820 | |||||
chr12:50814820
|
CT | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(105): Show | 113 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.671+399delT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50814820 | |||||
chr12:50814981
|
G | T | 116 | a0001c0002t0002g0002a0001c0002t0002g0012a0001c0002t0002g0018others(113): Show | 119 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.671+542G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814981 | ||||||
chr12:50814982
|
C | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0061 | 3 | HG02886.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.671+543C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814982 | ||||||
chr12:50814995
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.671+556G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50814995 | ||||||
chr12:50815132
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.671+693A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815132 | ||||||
chr12:50815180
|
T | G | 1 | a0001c0001t0001g0243 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.671+741T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815180 | ||||||
chr12:50815304
|
C | CTAGT | 118 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0002t0002g0002others(115): Show | 121 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.671+869_671+872dup others(4): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50815304 | |||||
chr12:50815384
|
T | C | 5 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0230others(2): Show | 5 | NA18957.hp2 NA18973.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+945T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815384 | ||||||
chr12:50815392
|
A | AT | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(7): Show | 10 | HG01256.hp1 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.671+964dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50815392 | |||||
chr12:50815397
|
T | C | 1 | a0001c0002t0002g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.671+958T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815397 | ||||||
chr12:50815552
|
A | AT | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.671+1127dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50815552 | |||||
chr12:50815822
|
T | G | 2 | a0001c0002t0002g0002a0001c0002t0002g0021 | 4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+1383T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815822 | ||||||
chr12:50815853
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 100 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.671+1414A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50815853 | ||||||
chr12:50816052
|
G | C | 1 | a0001c0001t0001g0278 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.671+1613G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816052 | ||||||
chr12:50816055
|
C | G | 65 | a0001c0002t0002g0012a0001c0002t0002g0018a0001c0002t0002g0095others(62): Show | 66 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.671+1616C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816055 | ||||||
chr12:50816082
|
C | T | 1 | a0001c0002t0002g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.671+1643C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816082 | ||||||
chr12:50816101
|
G | A | 1 | a0001c0002t0002g0191 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.671+1662G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816101 | ||||||
chr12:50816592
|
T | C | 16 | a0001c0001t0001g0118a0001c0001t0001g0214a0001c0001t0001g0216others(13): Show | 16 | HG00609.hp1 HG01109.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.671+2153T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816592 | ||||||
chr12:50816632
|
C | A | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(6): Show | 9 | HG02257.hp1 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2193C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816632 | ||||||
chr12:50816886
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.671+2447C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816886 | ||||||
chr12:50816981
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.671+2542C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50816981 | ||||||
chr12:50817116
|
G | T | 2 | a0001c0002t0007g0296a0001c0002t0007g0298 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.672-2519G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817116 | ||||||
chr12:50817285
|
A | G | 1 | a0001c0002t0002g0183 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.672-2350A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817285 | ||||||
chr12:50817366
|
A | G | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.672-2269A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817366 | ||||||
chr12:50817480
|
G | A | 21 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0325others(18): Show | 21 | HG01071.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.672-2155G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817480 | ||||||
chr12:50817532
|
A | G | 1 | a0001c0002t0002g0184 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.672-2103A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817532 | ||||||
chr12:50817755
|
A | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0317others(6): Show | 9 | HG02257.hp1 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-1880A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817755 | ||||||
chr12:50817909
|
A | G | 118 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0002t0002g0002others(115): Show | 121 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.672-1726A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817909 | ||||||
chr12:50817917
|
A | G | 2 | a0001c0001t0003g0010a0001c0001t0003g0087 | 3 | NA18947.hp2 NA18966.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.672-1718A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817917 | ||||||
chr12:50817944
|
T | A | 1 | a0001c0003t0004g0353 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.672-1691T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50817944 | ||||||
chr12:50817992
|
A | AT | 137 | a0001c0001t0009g0164a0001c0001t0009g0165a0001c0002t0001g0299others(134): Show | 140 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.672-1637dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50817992 | |||||
chr12:50818010
|
T | C | 6 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-1625T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818010 | ||||||
chr12:50818122
|
A | G | 2 | a0001c0002t0002g0129a0001c0002t0002g0156 | 2 | NA18985.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.672-1513A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818122 | ||||||
chr12:50818385
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.672-1250G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818385 | ||||||
chr12:50818495
|
G | GTAAGGAC others(9): Show |
1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1139_672-1138i others(18): Show |
ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50818495 | |||||
chr12:50818502
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1133T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818502 | ||||||
chr12:50818503
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1132G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818503 | ||||||
chr12:50818504
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1131T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818504 | ||||||
chr12:50818505
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1130G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818505 | ||||||
chr12:50818507
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1128G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818507 | ||||||
chr12:50818508
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1127G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818508 | ||||||
chr12:50818509
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1126G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818509 | ||||||
chr12:50818510
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1125G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818510 | ||||||
chr12:50818513
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1122A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818513 | ||||||
chr12:50818516
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1119T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818516 | ||||||
chr12:50818520
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1115G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818520 | ||||||
chr12:50818522
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1113A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818522 | ||||||
chr12:50818523
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1112C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818523 | ||||||
chr12:50818524
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1111A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818524 | ||||||
chr12:50818525
|
G | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1110G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818525 | ||||||
chr12:50818526
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1109T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818526 | ||||||
chr12:50818537
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1098A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818537 | ||||||
chr12:50818539
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1096G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818539 | ||||||
chr12:50818549
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1086A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818549 | ||||||
chr12:50818552
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1083C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818552 | ||||||
chr12:50818553
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1082A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818553 | ||||||
chr12:50818561
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1074A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818561 | ||||||
chr12:50818574
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1061T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818574 | ||||||
chr12:50818575
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1060A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818575 | ||||||
chr12:50818577
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1058A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818577 | ||||||
chr12:50818589
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1046T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818589 | ||||||
chr12:50818592
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1043T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818592 | ||||||
chr12:50818596
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1039A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818596 | ||||||
chr12:50818597
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1038T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818597 | ||||||
chr12:50818599
|
G | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1036G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818599 | ||||||
chr12:50818604
|
G | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1031G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818604 | ||||||
chr12:50818620
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1015C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818620 | ||||||
chr12:50818622
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-1013T>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818622 | ||||||
chr12:50818640
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-995T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818640 | ||||||
chr12:50818641
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-994G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818641 | ||||||
chr12:50818643
|
T | C | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-992T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818643 | ||||||
chr12:50818651
|
C | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-984C>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818651 | ||||||
chr12:50818653
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-982A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818653 | ||||||
chr12:50818654
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-981G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818654 | ||||||
chr12:50818670
|
C | T | 2 | a0001c0002t0002g0096a0001c0002t0002g0134 | 2 | HG00544.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.672-965C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818670 | ||||||
chr12:50818673
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-962G>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818673 | ||||||
chr12:50818673
|
G | C | 2 | a0001c0002t0002g0002a0001c0002t0002g0021 | 4 | HG02258.hp2 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-962G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818673 | ||||||
chr12:50818677
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-958T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818677 | ||||||
chr12:50818703
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-932A>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818703 | ||||||
chr12:50818705
|
C | G | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-930C>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818705 | ||||||
chr12:50818706
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-929T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818706 | ||||||
chr12:50818712
|
T | A | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-923T>A | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818712 | ||||||
chr12:50818713
|
G | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-922G>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818713 | ||||||
chr12:50818718
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-917T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818718 | ||||||
chr12:50818733
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-902C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818733 | ||||||
chr12:50818747
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-888T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818747 | ||||||
chr12:50818755
|
A | G | 1 | a0001c0001t0015g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.672-880A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818755 | ||||||
chr12:50818802
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-833T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818802 | ||||||
chr12:50818805
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-830C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818805 | ||||||
chr12:50818812
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-823G>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818812 | ||||||
chr12:50818814
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-821C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818814 | ||||||
chr12:50818828
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-807A>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818828 | ||||||
chr12:50818829
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-806C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818829 | ||||||
chr12:50818830
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.672-805T>C | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50818830 | ||||||
chr12:50819505
|
A | G | 1 | a0001c0003t0004g0345 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.672-130A>G | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50819505 | ||||||
chr12:50819604
|
C | T | 1 | a0001c0007t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672-31C>T | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | chr12 | 50819604 | ||||||
chr12:50819612
|
G | GT | 6 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0035others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-16dupT | ATF1 | ENSG00000123268.9 | transcript | ENST00000262053.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr12 | 50819612 |