geneid | 8091 |
---|---|
ensemblid | ENSG00000149948.14 |
hgncid | 5009 |
symbol | HMGA2 |
name | high mobility group AT-hook 2 |
refseq_nuc | NM_003483.6 |
refseq_prot | NP_003474.1 |
ensembl_nuc | ENST00000403681.7 |
ensembl_prot | ENSP00000384026.2 |
mane_status | MANE Select |
chr | chr12 |
start | 65824483 |
end | 65966291 |
strand | + |
ver | v1.2 |
region | chr12:65824483-65966291 |
region5000 | chr12:65819483-65971291 |
regionname0 | HMGA2_chr12_65824483_65966291 |
regionname5000 | HMGA2_chr12_65819483_65971291 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3784 | 13 | 0 | 1 | 8 | 0 | 4 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0002 | 0/0 | 3786 | 8 | 1 | 0 | 5 | 0 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0003 | 0/0 | 3790 | 7 | 4 | 2 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0004 | 0/0 | 3784 | 6 | 1 | 0 | 4 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0005 | 0/0 | 3785 | 6 | 1 | 0 | 4 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0006 | 0/0 | 3788 | 6 | 2 | 0 | 4 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0007 | 0/0 | 3788 | 5 | 0 | 3 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0008 | 0/0 | 3780 | 4 | 0 | 1 | 0 | 1 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0009 | 0/0 | 3794 | 4 | 1 | 0 | 3 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0010 | 0/0 | 3785 | 4 | 0 | 1 | 1 | 0 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0011 | 0/0 | 3786 | 4 | 2 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0012 | 0/0 | 3776 | 3 | 0 | 1 | 1 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0013 | 0/0 | 3778 | 3 | 0 | 0 | 2 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0014 | 0/0 | 3783 | 3 | 0 | 2 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0015 | 0/0 | 3780 | 3 | 0 | 0 | 2 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0016 | 0/0 | 3782 | 3 | 1 | 0 | 1 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0017 | 0/0 | 3788 | 3 | 1 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0018 | 0/0 | 3787 | 3 | 3 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0019 | 0/0 | 3791 | 3 | 0 | 2 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0020 | 0/0 | 3769 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0021 | 0/0 | 3772 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0022 | 0/0 | 3773 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0023 | 0/0 | 3772 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0024 | 0/0 | 3774 | 2 | 0 | 1 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0025 | 0/0 | 3775 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0026 | 0/0 | 3776 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0027 | 0/0 | 3779 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0028 | 0/0 | 3781 | 2 | 0 | 1 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0029 | 0/0 | 3778 | 2 | 1 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0030 | 0/0 | 3783 | 2 | 0 | 0 | 1 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0031 | 0/0 | 3782 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0032 | 0/0 | 3785 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0033 | 0/0 | 3784 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0034 | 0/1 | 3786 | 2 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0035 | 0/0 | 3785 | 2 | 1 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0036 | 0/0 | 3786 | 2 | 0 | 1 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0037 | 0/0 | 3789 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0038 | 0/0 | 3789 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0039 | 0/0 | 3791 | 2 | 0 | 2 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0040 | 0/0 | 3790 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0041 | 0/0 | 3795 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0042 | 0/0 | 3787 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0043 | 0/0 | 3789 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0044 | 0/0 | 3788 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0045 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0046 | 0/0 | 3781 | 2 | 1 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0047 | 0/0 | 3787 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0048 | 0/0 | 3790 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0049 | 0/0 | 3789 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0050 | 0/0 | 3771 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0051 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0052 | 0/0 | 3767 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0053 | 0/0 | 3764 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0054 | 0/0 | 3766 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0055 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0056 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0057 | 0/0 | 3770 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0058 | 0/0 | 3770 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0059 | 0/0 | 3775 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0060 | 0/0 | 3775 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0061 | 0/0 | 3774 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0062 | 0/0 | 3774 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0063 | 0/0 | 3779 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0064 | 0/0 | 3778 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0065 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0066 | 0/0 | 3778 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0067 | 0/0 | 3780 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0068 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0069 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0070 | 0/0 | 3781 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0071 | 0/0 | 3781 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0072 | 0/0 | 3783 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0073 | 0/0 | 3785 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0074 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0075 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0076 | 0/0 | 3783 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0077 | 0/0 | 3785 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0078 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0079 | 0/0 | 3787 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0080 | 0/0 | 3788 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0081 | 1/0 | 3788 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0082 | 0/0 | 3788 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0083 | 0/0 | 3787 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0084 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0085 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0086 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0087 | 0/0 | 3790 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0088 | 0/0 | 3793 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0089 | 0/0 | 3795 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0090 | 0/0 | 3792 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0091 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0092 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0093 | 0/0 | 3797 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0094 | 0/0 | 3800 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0095 | 0/0 | 3798 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0096 | 0/0 | 3802 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0097 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0098 | 0/0 | 3787 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0099 | 0/0 | 3784 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0100 | 0/0 | 3788 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0101 | 0/0 | 3787 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0102 | 0/0 | 3793 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0103 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0104 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0105 | 0/0 | 3780 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0106 | 0/0 | 3782 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0107 | 0/0 | 3787 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0108 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0109 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0110 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0111 | 0/0 | 3787 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0112 | 0/0 | 3788 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0113 | 0/0 | 3788 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0114 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0115 | 0/0 | 3791 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0116 | 0/0 | 3791 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0117 | 0/0 | 3792 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0118 | 0/0 | 3788 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0119 | 0/0 | 3793 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0120 | 0/0 | 3792 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0121 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0122 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0123 | 0/0 | 3792 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0124 | 0/0 | 3793 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0125 | 0/0 | 3796 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0126 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0127 | 0/0 | 3794 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0128 | 0/0 | 3796 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0129 | 0/0 | 3796 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0130 | 0/0 | 3799 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0131 | 0/0 | 3800 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0132 | 0/0 | 3774 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0133 | 0/0 | 3790 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
t0134 | 0/0 | 3800 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 330 | 235 | 64 | 36 | 95 | 8 | 30 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0002c0002 | 0/0 | 330 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4113 | 13 | 0 | 1 | 8 | 0 | 4 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0002 | 0/0 | 4115 | 8 | 1 | 0 | 5 | 0 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0003 | 0/0 | 4119 | 7 | 4 | 2 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0004 | 0/0 | 4113 | 6 | 1 | 0 | 4 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0005 | 0/0 | 4114 | 6 | 1 | 0 | 4 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0006 | 0/0 | 4117 | 6 | 2 | 0 | 4 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0007 | 0/0 | 4117 | 5 | 0 | 3 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0008 | 0/0 | 4109 | 4 | 0 | 1 | 0 | 1 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0009 | 0/0 | 4123 | 4 | 1 | 0 | 3 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0010 | 0/0 | 4114 | 4 | 0 | 1 | 1 | 0 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0011 | 0/0 | 4115 | 4 | 2 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0012 | 0/0 | 4105 | 3 | 0 | 1 | 1 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0013 | 0/0 | 4107 | 3 | 0 | 0 | 2 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0014 | 0/0 | 4112 | 3 | 0 | 2 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0015 | 0/0 | 4109 | 3 | 0 | 0 | 2 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0016 | 0/0 | 4111 | 3 | 1 | 0 | 1 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0017 | 0/0 | 4117 | 3 | 1 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0018 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0019 | 0/0 | 4120 | 3 | 0 | 2 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0020 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0021 | 0/0 | 4101 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0022 | 0/0 | 4102 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0023 | 0/0 | 4101 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0024 | 0/0 | 4103 | 2 | 0 | 1 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0025 | 0/0 | 4104 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0026 | 0/0 | 4105 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0027 | 0/0 | 4108 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0028 | 0/0 | 4110 | 2 | 0 | 1 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0029 | 0/0 | 4107 | 2 | 1 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0030 | 0/0 | 4112 | 2 | 0 | 0 | 1 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0031 | 0/0 | 4111 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0032 | 0/0 | 4114 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0033 | 0/0 | 4113 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0034 | 0/1 | 4115 | 2 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0035 | 0/0 | 4114 | 2 | 1 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0036 | 0/0 | 4115 | 2 | 0 | 1 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0037 | 0/0 | 4118 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0038 | 0/0 | 4118 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0039 | 0/0 | 4120 | 2 | 0 | 2 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0040 | 0/0 | 4119 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0041 | 0/0 | 4124 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0042 | 0/0 | 4116 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0043 | 0/0 | 4118 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0044 | 0/0 | 4117 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0045 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0046 | 0/0 | 4110 | 2 | 1 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0047 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0048 | 0/0 | 4119 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0049 | 0/0 | 4118 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0050 | 0/0 | 4100 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0051 | 0/0 | 4094 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0052 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0053 | 0/0 | 4093 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0054 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0055 | 0/0 | 4094 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0056 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0057 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0058 | 0/0 | 4099 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0059 | 0/0 | 4104 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0060 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0061 | 0/0 | 4103 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0062 | 0/0 | 4103 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0063 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0064 | 0/0 | 4107 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0065 | 0/0 | 4105 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0066 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0067 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0068 | 0/0 | 4108 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0069 | 0/0 | 4107 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0070 | 0/0 | 4110 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0071 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0072 | 0/0 | 4112 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0073 | 0/0 | 4114 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0074 | 0/0 | 4115 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0075 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0076 | 0/0 | 4112 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0077 | 0/0 | 4114 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0078 | 0/0 | 4115 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0079 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0080 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0081 | 1/0 | 4117 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0082 | 0/0 | 4117 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0083 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0084 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0085 | 0/0 | 4119 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0086 | 0/0 | 4119 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0087 | 0/0 | 4119 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0088 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0089 | 0/0 | 4124 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0090 | 0/0 | 4121 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0091 | 0/0 | 4124 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0092 | 0/0 | 4124 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0093 | 0/0 | 4126 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0094 | 0/0 | 4129 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0095 | 0/0 | 4127 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0096 | 0/0 | 4131 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0097 | 0/0 | 4111 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0098 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0099 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0100 | 0/0 | 4117 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0101 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0102 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0103 | 0/0 | 4121 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0104 | 0/0 | 4112 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0105 | 0/0 | 4109 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0106 | 0/0 | 4111 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0107 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0108 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0109 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0110 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0111 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0112 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0113 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0114 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0115 | 0/0 | 4120 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0116 | 0/0 | 4120 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0117 | 0/0 | 4121 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0118 | 0/0 | 4117 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0119 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0120 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0121 | 0/0 | 4121 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0122 | 0/0 | 4121 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0123 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0124 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0125 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0126 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0127 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0128 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0129 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0130 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0131 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0132 | 0/0 | 4103 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0133 | 0/0 | 4119 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0001c0001t0134 | 0/0 | 4129 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
a0002c0002t0020 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | copy fasta | chr12 | 65819483 | 65971291 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0007g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0007g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0008g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0009g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0010g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0010g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0010g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0010g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0012g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0014g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0014g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0014g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0015g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0015g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0015g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0016g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0017g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0017g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0017g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0018g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0018g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0018g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0019g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0019g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0019g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0020g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0021g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0022g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0022g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0023g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0023g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0024g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0024g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0025g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0025g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0026g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0026g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0027g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0027g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0028g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0028g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0029g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0029g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0030g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0030g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0031g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0031g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0032g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0032g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0033g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0033g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0034g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0034g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0035g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0035g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0036g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0036g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0037g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0037g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0038g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0038g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0039g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0039g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0040g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0040g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0041g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0042g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0042g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0043g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0043g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0044g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0044g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0045g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0045g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0046g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0046g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0047g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0047g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0048g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0048g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0049g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0049g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0050g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0051g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0052g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0053g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0054g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0055g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0056g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0057g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0058g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0059g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0060g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0061g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0062g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0063g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0064g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0065g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0066g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0067g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0068g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0069g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0070g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0071g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0072g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0073g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0074g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0075g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0076g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0077g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0078g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0079g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0080g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0081g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0082g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0083g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0084g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0085g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0086g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0087g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0088g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0089g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0090g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0091g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0092g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0093g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0094g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0095g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0096g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0097g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0098g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0099g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0100g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0101g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0102g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0103g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0104g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0105g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0106g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0107g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0108g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0109g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0110g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0111g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0112g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0113g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0114g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0115g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0116g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0117g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0118g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0119g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0120g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0121g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0122g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0123g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0124g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0125g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0126g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0127g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0128g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0129g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0130g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0131g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0132g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0133g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0001c0001t0134g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
a0002c0002t0020g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0015 | g0149 | EUR | GBR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00140 | hp2 | a0001 | c0001 | t0078 | g0122 | EUR | GBR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00280 | hp1 | a0001 | c0001 | t0096 | g0234 | EUR | FIN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00280 | hp2 | a0001 | c0001 | t0016 | g0119 | EUR | FIN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00423 | hp1 | a0001 | c0001 | t0075 | g0137 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00423 | hp2 | a0001 | c0001 | t0114 | g0206 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00558 | hp1 | a0001 | c0001 | t0099 | g0011 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00609 | hp2 | a0001 | c0001 | t0017 | g0194 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00621 | hp1 | a0001 | c0001 | t0077 | g0195 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00621 | hp2 | a0001 | c0001 | t0015 | g0140 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00673 | hp1 | a0001 | c0001 | t0013 | g0153 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00673 | hp2 | a0001 | c0001 | t0050 | g0145 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0022 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00733 | hp2 | a0001 | c0001 | t0059 | g0128 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00735 | hp1 | a0001 | c0001 | t0039 | g0127 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00735 | hp2 | a0001 | c0001 | t0062 | g0163 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00741 | hp1 | a0001 | c0001 | t0028 | g0231 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG00741 | hp2 | a0001 | c0001 | t0089 | g0083 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01069 | hp1 | a0001 | c0001 | t0069 | g0144 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01069 | hp2 | a0001 | c0001 | t0082 | g0084 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0021 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0161 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01074 | hp1 | a0001 | c0001 | t0065 | g0081 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0017 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01167 | hp1 | a0001 | c0001 | t0124 | g0166 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0112 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01169 | hp1 | a0001 | c0001 | t0072 | g0162 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01169 | hp2 | a0001 | c0001 | t0019 | g0211 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01192 | hp1 | a0001 | c0001 | t0019 | g0207 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01192 | hp2 | a0001 | c0001 | t0010 | g0031 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01243 | hp1 | a0001 | c0001 | t0068 | g0175 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01243 | hp2 | a0001 | c0001 | t0061 | g0079 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01256 | hp2 | a0001 | c0001 | t0012 | g0131 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01258 | hp1 | a0001 | c0001 | t0095 | g0103 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01261 | hp1 | a0001 | c0001 | t0117 | g0202 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01261 | hp2 | a0001 | c0001 | t0014 | g0142 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01361 | hp1 | a0001 | c0001 | t0039 | g0106 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01361 | hp2 | a0001 | c0001 | t0116 | g0219 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01433 | hp1 | a0001 | c0001 | t0073 | g0165 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01433 | hp2 | a0001 | c0001 | t0070 | g0118 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01496 | hp2 | a0001 | c0001 | t0088 | g0133 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0208 | EUR | IBS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01516 | hp2 | a0001 | c0001 | t0094 | g0235 | EUR | IBS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01884 | hp1 | a0001 | c0001 | t0121 | g0005 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01884 | hp2 | a0001 | c0001 | t0130 | g0226 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01891 | hp1 | a0001 | c0001 | t0127 | g0006 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01891 | hp2 | a0001 | c0001 | t0029 | g0082 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01978 | hp1 | a0001 | c0001 | t0090 | g0078 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG01978 | hp2 | a0001 | c0001 | t0024 | g0110 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02027 | hp1 | a0002 | c0002 | t0020 | g0099 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02027 | hp2 | a0001 | c0001 | t0133 | g0087 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02040 | hp2 | a0001 | c0001 | t0023 | g0108 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02074 | hp1 | a0001 | c0001 | t0015 | g0075 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02074 | hp2 | a0001 | c0001 | t0024 | g0155 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02083 | hp1 | a0001 | c0001 | t0031 | g0151 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02132 | hp2 | a0001 | c0001 | t0022 | g0109 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02135 | hp1 | a0001 | c0001 | t0030 | g0136 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02135 | hp2 | a0001 | c0001 | t0010 | g0057 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02155 | hp1 | a0001 | c0001 | t0066 | g0135 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02155 | hp2 | a0001 | c0001 | t0126 | g0212 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02165 | hp2 | a0001 | c0001 | t0026 | g0154 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02257 | hp1 | a0001 | c0001 | t0111 | g0227 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02257 | hp2 | a0001 | c0001 | t0057 | g0233 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02258 | hp1 | a0001 | c0001 | t0086 | g0217 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02258 | hp2 | a0001 | c0001 | t0085 | g0143 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02300 | hp1 | a0001 | c0001 | t0036 | g0077 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02300 | hp2 | a0001 | c0001 | t0087 | g0086 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02451 | hp2 | a0001 | c0001 | t0102 | g0218 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02615 | hp1 | a0001 | c0001 | t0021 | g0171 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02615 | hp2 | a0001 | c0001 | t0115 | g0007 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02622 | hp1 | a0001 | c0001 | t0021 | g0170 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02622 | hp2 | a0001 | c0001 | t0098 | g0030 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02630 | hp1 | a0001 | c0001 | t0035 | g0229 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02630 | hp2 | a0001 | c0001 | t0016 | g0123 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02647 | hp1 | a0001 | c0001 | t0080 | g0048 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02647 | hp2 | a0001 | c0001 | t0122 | g0230 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02683 | hp1 | a0001 | c0001 | t0106 | g0167 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02698 | hp1 | a0001 | c0001 | t0120 | g0203 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02717 | hp1 | a0001 | c0001 | t0043 | g0018 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02717 | hp2 | a0001 | c0001 | t0025 | g0173 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02735 | hp1 | a0001 | c0001 | t0118 | g0232 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02735 | hp2 | a0001 | c0001 | t0019 | g0209 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02738 | hp1 | a0001 | c0001 | t0030 | g0147 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02809 | hp1 | a0001 | c0001 | t0046 | g0169 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02809 | hp2 | a0001 | c0001 | t0060 | g0172 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0027 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02896 | hp1 | a0001 | c0001 | t0053 | g0010 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02896 | hp2 | a0001 | c0001 | t0084 | g0002 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02922 | hp1 | a0001 | c0001 | t0049 | g0186 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02922 | hp2 | a0001 | c0001 | t0110 | g0182 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02965 | hp1 | a0001 | c0001 | t0131 | g0222 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02976 | hp2 | a0001 | c0001 | t0047 | g0183 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03017 | hp2 | a0001 | c0001 | t0035 | g0148 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03041 | hp1 | a0001 | c0001 | t0104 | g0216 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03041 | hp2 | a0001 | c0001 | t0018 | g0223 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03098 | hp1 | a0001 | c0001 | t0052 | g0178 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03098 | hp2 | a0001 | c0001 | t0119 | g0008 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03139 | hp1 | a0001 | c0001 | t0103 | g0019 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03139 | hp2 | a0001 | c0001 | t0051 | g0176 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03209 | hp1 | a0001 | c0001 | t0113 | g0181 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03209 | hp2 | a0001 | c0001 | t0109 | g0012 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03225 | hp1 | a0001 | c0001 | t0054 | g0177 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03225 | hp2 | a0001 | c0001 | t0018 | g0225 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03239 | hp2 | a0001 | c0001 | t0123 | g0200 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03490 | hp1 | a0001 | c0001 | t0105 | g0168 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03490 | hp2 | a0001 | c0001 | t0074 | g0150 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03540 | hp2 | a0001 | c0001 | t0045 | g0050 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03579 | hp2 | a0001 | c0001 | t0107 | g0220 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03669 | hp1 | a0001 | c0001 | t0063 | g0164 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03669 | hp2 | a0001 | c0001 | t0125 | g0210 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0040 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03831 | hp2 | a0001 | c0001 | t0013 | g0107 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0130 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04115 | hp1 | a0001 | c0001 | t0029 | g0160 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0044 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04184 | hp2 | a0001 | c0001 | t0046 | g0184 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04204 | hp1 | a0001 | c0001 | t0128 | g0189 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04204 | hp2 | a0001 | c0001 | t0008 | g0139 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG04228 | hp2 | a0001 | c0001 | t0028 | g0101 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18522 | hp1 | a0001 | c0001 | t0108 | g0180 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18906 | hp1 | a0001 | c0001 | t0044 | g0052 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18941 | hp2 | a0001 | c0001 | t0033 | g0093 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18942 | hp1 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18942 | hp2 | a0001 | c0001 | t0020 | g0100 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18943 | hp1 | a0001 | c0001 | t0091 | g0129 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18943 | hp2 | a0001 | c0001 | t0037 | g0201 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18948 | hp1 | a0001 | c0001 | t0027 | g0158 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18951 | hp2 | a0001 | c0001 | t0040 | g0091 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18952 | hp1 | a0001 | c0001 | t0049 | g0191 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18952 | hp2 | a0001 | c0001 | t0012 | g0111 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18953 | hp1 | a0001 | c0001 | t0040 | g0120 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18960 | hp1 | a0001 | c0001 | t0132 | g0028 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18960 | hp2 | a0001 | c0001 | t0071 | g0092 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18961 | hp1 | a0001 | c0001 | t0076 | g0205 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18961 | hp2 | a0001 | c0001 | t0017 | g0105 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18967 | hp1 | a0001 | c0001 | t0067 | g0138 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18967 | hp2 | a0001 | c0001 | t0048 | g0199 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18970 | hp2 | a0001 | c0001 | t0011 | g0066 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18971 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18971 | hp2 | a0001 | c0001 | t0036 | g0098 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18972 | hp1 | a0001 | c0001 | t0056 | g0116 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18972 | hp2 | a0001 | c0001 | t0100 | g0020 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18978 | hp1 | a0001 | c0001 | t0042 | g0071 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18978 | hp2 | a0001 | c0001 | t0041 | g0179 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18981 | hp2 | a0001 | c0001 | t0058 | g0152 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18984 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0124 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18988 | hp1 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18988 | hp2 | a0001 | c0001 | t0011 | g0067 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18991 | hp1 | a0001 | c0001 | t0027 | g0157 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18991 | hp2 | a0001 | c0001 | t0083 | g0088 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18992 | hp1 | a0001 | c0001 | t0026 | g0097 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18994 | hp1 | a0001 | c0001 | t0031 | g0089 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA18994 | hp2 | a0001 | c0001 | t0093 | g0095 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19001 | hp1 | a0001 | c0001 | t0037 | g0141 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19001 | hp2 | a0001 | c0001 | t0097 | g0024 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19002 | hp1 | a0001 | c0001 | t0041 | g0001 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19002 | hp2 | a0001 | c0001 | t0022 | g0146 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19003 | hp2 | a0001 | c0001 | t0023 | g0132 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19010 | hp1 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19010 | hp2 | a0001 | c0001 | t0013 | g0156 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19011 | hp2 | a0001 | c0001 | t0033 | g0096 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19030 | hp1 | a0001 | c0001 | t0101 | g0043 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19030 | hp2 | a0001 | c0001 | t0047 | g0185 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19043 | hp1 | a0001 | c0001 | t0044 | g0051 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19043 | hp2 | a0001 | c0001 | t0055 | g0221 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19056 | hp1 | a0001 | c0001 | t0016 | g0113 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19063 | hp1 | a0001 | c0001 | t0079 | g0117 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19063 | hp2 | a0001 | c0001 | t0038 | g0193 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19065 | hp2 | a0001 | c0001 | t0092 | g0192 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19078 | hp1 | a0001 | c0001 | t0043 | g0026 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19078 | hp2 | a0001 | c0001 | t0014 | g0159 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19079 | hp1 | a0001 | c0001 | t0032 | g0121 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0072 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19080 | hp2 | a0001 | c0001 | t0038 | g0115 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19083 | hp1 | a0001 | c0001 | t0048 | g0215 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19083 | hp2 | a0001 | c0001 | t0032 | g0134 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19088 | hp1 | a0001 | c0001 | t0134 | g0114 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20129 | hp1 | a0001 | c0001 | t0017 | g0102 | AFR | ASW | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20129 | hp2 | a0001 | c0001 | t0018 | g0013 | AFR | ASW | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20752 | hp1 | a0001 | c0001 | t0008 | g0080 | EUR | TSI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20752 | hp2 | a0001 | c0001 | t0064 | g0016 | EUR | TSI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0090 | SAS | GIH | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20905 | hp2 | a0001 | c0001 | t0034 | g0126 | SAS | GIH | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG02559 | hp2 | a0001 | c0001 | t0112 | g0224 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03471 | hp1 | a0001 | c0001 | t0042 | g0047 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
HG03471 | hp2 | a0001 | c0001 | t0025 | g0174 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20300 | hp1 | a0001 | c0001 | t0009 | g0104 | AFR | USA | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | USA | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA21309 | hp1 | a0001 | c0001 | t0045 | g0055 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
NA21309 | hp2 | a0001 | c0001 | t0129 | g0196 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0034 | g0094 | REF | REF | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0081 | g0125 | REF | REF | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:65963279
|
C | G | 1 | a0002 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.317C>G | p.Ala106Gly | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1105/4117 | 317/330 | 106/109 | chr12 | 65963279 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:65824546
|
C | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-725C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 725 | chr12 | 65824546 | |||||
chr12:65824618
|
C | T | 1 | a0001c0001t0133 | 1 | HG02027.hp2 | 5_prime_UTR_variant | MODIFIER | c.-653C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 653 | chr12 | 65824618 | |||||
chr12:65824708
|
ATCTCTTC others(8): Show |
A | 1 | a0001c0001t0050 | 1 | HG00673.hp2 | 5_prime_UTR_variant | MODIFIER | c.-557_-543delTCTCTC others(9): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 543 | INFO_REALIGN_3_PRIME | chr12 | 65824708 | ||||
chr12:65824713
|
T | TTC | 5 | a0001c0001t0017a0001c0001t0037a0001c0001t0038others(2): Show | 9 | HG00609.hp2 HG02258.hp1 HG02258.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-503_-502dupTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
T | TTCTC | 5 | a0001c0001t0039a0001c0001t0040a0001c0001t0087others(2): Show | 7 | HG00735.hp1 HG01361.hp1 HG02027.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-505_-502dupTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
T | TTCTCTC | 3 | a0001c0001t0088a0001c0001t0089a0001c0001t0090 | 3 | HG00741.hp2 HG01496.hp2 HG01978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-507_-502dupTCTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
T | TTCTCTCT others(1): Show |
4 | a0001c0001t0009a0001c0001t0041a0001c0001t0091others(1): Show | 8 | NA18943.hp1 NA18971.hp1 NA18978.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-509_-502dupTCTCTC others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
T | TTCTCTCT others(3): Show |
1 | a0001c0001t0093 | 1 | NA18994.hp2 | 5_prime_UTR_variant | MODIFIER | c.-511_-502dupTCTCTC others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
T | TTCTCTCT others(5): Show |
2 | a0001c0001t0094a0001c0001t0095 | 2 | HG01258.hp1 HG01516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-513_-502dupTCTCTC others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
T | TTCTCTCT others(7): Show |
1 | a0001c0001t0096 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-515_-502dupTCTCTC others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTC | T | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | 61 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-503_-502delTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTC | T | 8 | a0001c0001t0030a0001c0001t0031a0001c0001t0072others(5): Show | 10 | HG00423.hp1 HG01169.hp1 HG01433.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-505_-502delTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTC | T | 10 | a0001c0001t0008a0001c0001t0014a0001c0001t0015others(7): Show | 20 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-507_-502delTCTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTCT others(1): Show |
T | 8 | a0001c0001t0013a0001c0001t0027a0001c0001t0028others(5): Show | 13 | HG00673.hp1 HG00741.hp1 HG01069.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-509_-502delTCTCTC others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTCT others(3): Show |
T | 4 | a0001c0001t0026a0001c0001t0063a0001c0001t0064others(1): Show | 5 | HG01074.hp1 HG02165.hp2 HG03669.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-511_-502delTCTCTC others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTCT others(5): Show |
T | 7 | a0001c0001t0012a0001c0001t0024a0001c0001t0025others(4): Show | 11 | HG00735.hp2 HG01243.hp2 HG01256.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-513_-502delTCTCTC others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTCT others(7): Show |
T | 3 | a0001c0001t0022a0001c0001t0023a0001c0001t0059 | 5 | HG00733.hp2 HG02040.hp2 HG02132.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-515_-502delTCTCTC others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTCT others(9): Show |
T | 2 | a0001c0001t0021a0001c0001t0058 | 3 | HG02615.hp1 HG02622.hp1 NA18981.hp2 |
5_prime_UTR_variant | MODIFIER | c.-517_-502delTCTCTC others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTCT others(11): Show |
T | 4 | a0001c0001t0020a0001c0001t0056a0001c0001t0057others(1): Show | 4 | HG02027.hp1 HG02257.hp2 NA18942.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-519_-502delTCTCTC others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824713
|
TTCTCTCT others(15): Show |
T | 5 | a0001c0001t0051a0001c0001t0052a0001c0001t0053others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03139.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-523_-502delTCTCTC others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | ||||
chr12:65824721
|
C | CTCTCTCT others(5): Show |
1 | a0001c0001t0131 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824721 | ||||
chr12:65824723
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0130 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824723 | ||||
chr12:65824725
|
C | CTCTCTCT others(1): Show |
2 | a0001c0001t0128a0001c0001t0129 | 2 | HG04204.hp1 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824725 | ||||
chr12:65824727
|
C | CTCTCTG | 3 | a0001c0001t0125a0001c0001t0126a0001c0001t0127 | 3 | HG01891.hp1 HG02155.hp2 HG03669.hp2 |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824727 | ||||
chr12:65824729
|
C | CTCTG | 6 | a0001c0001t0119a0001c0001t0120a0001c0001t0121others(3): Show | 6 | HG01167.hp1 HG01884.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824729 | ||||
chr12:65824731
|
C | CTG | 10 | a0001c0001t0003a0001c0001t0006a0001c0001t0019others(7): Show | 25 | HG00423.hp2 HG01169.hp2 HG01192.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824731 | ||||
chr12:65824733
|
C | CTCTG | 2 | a0001c0001t0102a0001c0001t0103 | 2 | HG02451.hp2 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-535_-534insGTCT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 534 | INFO_REALIGN_3_PRIME | chr12 | 65824733 | ||||
chr12:65824733
|
C | G | 4 | a0001c0001t0018a0001c0001t0111a0001c0001t0112others(1): Show | 6 | HG02257.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-538C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824733 | ||||||
chr12:65824735
|
C | CTG | 1 | a0001c0001t0045 | 2 | HG03540.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-535_-534insGT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 534 | INFO_REALIGN_3_PRIME | chr12 | 65824735 | ||||
chr12:65824735
|
C | G | 5 | a0001c0001t0047a0001c0001t0107a0001c0001t0108others(2): Show | 6 | HG02922.hp2 HG02976.hp2 HG03209.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-536C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824735 | ||||||
chr12:65824737
|
C | G | 5 | a0001c0001t0007a0001c0001t0043a0001c0001t0044others(2): Show | 11 | HG00733.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-534C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824737 | ||||||
chr12:65824739
|
C | G | 14 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | 51 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-532C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824739 | ||||||
chr12:65824741
|
C | G | 1 | a0001c0001t0097 | 1 | NA19001.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-530C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824741 | ||||||
chr12:65824877
|
G | T | 1 | a0001c0001t0084 | 1 | HG02896.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-394G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824877 | ||||||
chr12:65824905
|
C | T | 1 | a0001c0001t0078 | 1 | HG00140.hp2 | 5_prime_UTR_variant | MODIFIER | c.-366C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 366 | chr12 | 65824905 | |||||
chr12:65825019
|
C | T | 2 | a0001c0001t0062a0001c0001t0069 | 2 | HG00735.hp2 HG01069.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65825019 | ||||||
chr12:65825124
|
G | C | 1 | a0001c0001t0066 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-147G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 147 | chr12 | 65825124 | |||||
chr12:65963427
|
A | AG | 41 | a0001c0001t0010a0001c0001t0014a0001c0001t0020others(38): Show | 58 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*143dupG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 144 | INFO_REALIGN_3_PRIME | chr12 | 65963427 | ||||
chr12:65963427
|
AG | A | 15 | a0001c0001t0005a0001c0001t0018a0001c0001t0025others(12): Show | 27 | HG01243.hp1 HG02630.hp1 HG02717.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*143delG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 143 | INFO_REALIGN_3_PRIME | chr12 | 65963427 | ||||
chr12:65963431
|
G | T | 14 | a0001c0001t0001a0001c0001t0008a0001c0001t0029others(11): Show | 31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*139G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 139 | chr12 | 65963431 | |||||
chr12:65963786
|
T | A | 1 | a0001c0001t0077 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 494 | chr12 | 65963786 | |||||
chr12:65964007
|
A | G | 1 | a0001c0001t0060 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 715 | chr12 | 65964007 | |||||
chr12:65964008
|
C | T | 6 | a0001c0001t0047a0001c0001t0086a0001c0001t0102others(3): Show | 7 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*716C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 716 | chr12 | 65964008 | |||||
chr12:65964166
|
A | T | 4 | a0001c0001t0019a0001c0001t0082a0001c0001t0124others(1): Show | 6 | HG01069.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*874A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 874 | chr12 | 65964166 | |||||
chr12:65964299
|
A | AG | 6 | a0001c0001t0019a0001c0001t0059a0001c0001t0074others(3): Show | 8 | HG00733.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1008insG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1008 | chr12 | 65964299 | |||||
chr12:65964299
|
AAG | A | 13 | a0001c0001t0001a0001c0001t0008a0001c0001t0029others(10): Show | 29 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1008_*1009delAG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1008 | chr12 | 65964299 | |||||
chr12:65964300
|
A | G | 7 | a0001c0001t0019a0001c0001t0059a0001c0001t0074others(4): Show | 9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1008A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1008 | chr12 | 65964300 | |||||
chr12:65964339
|
CTT | C | 45 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(42): Show | 82 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1048_*1049delTT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1048 | chr12 | 65964339 | |||||
chr12:65964467
|
T | G | 1 | a0001c0001t0120 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1175 | chr12 | 65964467 | |||||
chr12:65964567
|
C | T | 78 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(75): Show | 135 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1275C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1275 | chr12 | 65964567 | |||||
chr12:65964750
|
A | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1458A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1458 | chr12 | 65964750 | |||||
chr12:65964760
|
T | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1468T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1468 | chr12 | 65964760 | |||||
chr12:65964762
|
C | A | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1470 | chr12 | 65964762 | |||||
chr12:65964765
|
G | A | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1473G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1473 | chr12 | 65964765 | |||||
chr12:65964774
|
T | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1482T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1482 | chr12 | 65964774 | |||||
chr12:65964791
|
C | A | 2 | a0001c0001t0070a0001c0001t0072 | 2 | HG01169.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1499C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1499 | chr12 | 65964791 | |||||
chr12:65964800
|
G | A | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1508G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1508 | chr12 | 65964800 | |||||
chr12:65964801
|
A | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1509A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1509 | chr12 | 65964801 | |||||
chr12:65964871
|
A | T | 1 | a0001c0001t0087 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1579A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1579 | chr12 | 65964871 | |||||
chr12:65964962
|
A | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1670A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1670 | chr12 | 65964962 | |||||
chr12:65964963
|
C | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1671 | chr12 | 65964963 | |||||
chr12:65964964
|
C | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1672 | chr12 | 65964964 | |||||
chr12:65964966
|
C | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1674C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1674 | chr12 | 65964966 | |||||
chr12:65964967
|
C | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1675C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1675 | chr12 | 65964967 | |||||
chr12:65964969
|
G | A | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1677 | chr12 | 65964969 | |||||
chr12:65964971
|
C | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1679 | chr12 | 65964971 | |||||
chr12:65964976
|
A | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1684A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1684 | chr12 | 65964976 | |||||
chr12:65964977
|
A | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1685 | chr12 | 65964977 | |||||
chr12:65964978
|
A | C | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1686 | chr12 | 65964978 | |||||
chr12:65964979
|
G | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1687G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1687 | chr12 | 65964979 | |||||
chr12:65964981
|
A | C | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1689A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1689 | chr12 | 65964981 | |||||
chr12:65964982
|
A | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1690A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1690 | chr12 | 65964982 | |||||
chr12:65964991
|
T | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1699 | chr12 | 65964991 | |||||
chr12:65965051
|
T | A | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1759T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1759 | chr12 | 65965051 | |||||
chr12:65965058
|
A | C | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1766 | chr12 | 65965058 | |||||
chr12:65965066
|
T | G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1774 | chr12 | 65965066 | |||||
chr12:65965121
|
GTAAATAA others(19): Show |
G | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1830_*1855delTAAA others(22): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1830 | chr12 | 65965121 | |||||
chr12:65965148
|
C | T | 1 | a0001c0001t0123 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1856C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1856 | chr12 | 65965148 | |||||
chr12:65965152
|
C | CTTCTAGG others(29): Show |
1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860_*1861insTTCT others(32): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1861 | chr12 | 65965152 | |||||
chr12:65965153
|
A | C | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1861A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1861 | chr12 | 65965153 | |||||
chr12:65965180
|
A | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1888 | chr12 | 65965180 | |||||
chr12:65965187
|
A | G | 1 | a0001c0001t0099 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1895A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1895 | chr12 | 65965187 | |||||
chr12:65965228
|
T | C | 1 | a0001c0001t0086 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1936T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1936 | chr12 | 65965228 | |||||
chr12:65965274
|
A | T | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1982 | chr12 | 65965274 | |||||
chr12:65965275
|
T | A | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1983 | chr12 | 65965275 | |||||
chr12:65965276
|
T | A | 1 | a0001c0001t0134 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1984T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1984 | chr12 | 65965276 | |||||
chr12:65965403
|
C | T | 1 | a0001c0001t0091 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2111C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2111 | chr12 | 65965403 | |||||
chr12:65965594
|
A | G | 1 | a0001c0001t0053 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2302A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2302 | chr12 | 65965594 | |||||
chr12:65965964
|
C | T | 4 | a0001c0001t0047a0001c0001t0086a0001c0001t0110others(1): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2672C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2672 | chr12 | 65965964 | |||||
chr12:65965972
|
C | A | 101 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(98): Show | 175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2680C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2680 | chr12 | 65965972 | |||||
chr12:65966128
|
T | C | 1 | a0001c0001t0130 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2836T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2836 | chr12 | 65966128 | |||||
chr12:65966288
|
C | T | 45 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(42): Show | 82 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2996C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2996 | chr12 | 65966288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:65825466
|
G | A | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.111+85G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825466 | ||||||
chr12:65825466
|
G | C | 7 | a0001c0001t0003g0009a0001c0001t0006g0003a0001c0001t0006g0004others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+85G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825466 | ||||||
chr12:65825519
|
C | G | 2 | a0001c0001t0094g0235a0001c0001t0096g0234 | 2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.111+138C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825519 | ||||||
chr12:65825596
|
C | T | 1 | a0001c0001t0057g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111+215C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825596 | ||||||
chr12:65826042
|
G | T | 2 | a0001c0001t0028g0231a0001c0001t0118g0232 | 2 | HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.111+661G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826042 | ||||||
chr12:65826045
|
G | A | 1 | a0001c0001t0053g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.111+664G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826045 | ||||||
chr12:65826052
|
G | C | 1 | a0001c0001t0028g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.111+671G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826052 | ||||||
chr12:65826143
|
T | A | 1 | a0001c0001t0099g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.111+762T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826143 | ||||||
chr12:65826364
|
G | C | 1 | a0001c0001t0028g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.111+983G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826364 | ||||||
chr12:65826485
|
A | C | 1 | a0001c0001t0122g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.111+1104A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826485 | ||||||
chr12:65826486
|
T | C | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.111+1105T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826486 | ||||||
chr12:65826568
|
T | C | 2 | a0001c0001t0005g0014a0001c0001t0005g0015 | 2 | NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.111+1187T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826568 | ||||||
chr12:65826660
|
T | C | 1 | a0001c0001t0064g0016 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111+1279T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826660 | ||||||
chr12:65826686
|
T | C | 3 | a0001c0001t0007g0017a0001c0001t0043g0018a0001c0001t0103g0019 | 3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.111+1305T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826686 | ||||||
chr12:65826727
|
C | T | 1 | a0001c0001t0035g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112-1274C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826727 | ||||||
chr12:65826754
|
T | C | 63 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.112-1247T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826754 | ||||||
chr12:65826780
|
C | CA | 10 | a0001c0001t0008g0080a0001c0001t0009g0085a0001c0001t0029g0082others(7): Show | 10 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.112-1205dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65826780 | |||||
chr12:65826780
|
CA | C | 66 | a0001c0001t0003g0009a0001c0001t0003g0187a0001c0001t0003g0188others(63): Show | 66 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.112-1205delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65826780 | |||||
chr12:65826780
|
CAA | C | 13 | a0001c0001t0006g0228a0001c0001t0018g0013a0001c0001t0018g0223others(10): Show | 13 | HG01361.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.112-1206_112-1205d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65826780 | |||||
chr12:65827029
|
C | T | 1 | a0001c0001t0102g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112-972C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827029 | ||||||
chr12:65827208
|
C | T | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.112-793C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827208 | ||||||
chr12:65827241
|
C | T | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.112-760C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827241 | ||||||
chr12:65827247
|
T | G | 10 | a0001c0001t0003g0009a0001c0001t0006g0003a0001c0001t0006g0004others(7): Show | 10 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.112-754T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827247 | ||||||
chr12:65827280
|
A | T | 63 | a0001c0001t0003g0009a0001c0001t0003g0187a0001c0001t0003g0188others(60): Show | 63 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.112-721A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827280 | ||||||
chr12:65827282
|
A | G | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.112-719A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827282 | ||||||
chr12:65827484
|
T | C | 1 | a0001c0001t0087g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.112-517T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827484 | ||||||
chr12:65827540
|
T | TAC | 63 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.112-460_112-459ins others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65827540 | |||||
chr12:65827666
|
G | C | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.112-335G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827666 | ||||||
chr12:65827674
|
A | G | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.112-327A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827674 | ||||||
chr12:65827928
|
T | C | 1 | a0001c0001t0108g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-73T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827928 | ||||||
chr12:65827952
|
C | A | 2 | a0001c0001t0007g0021a0001c0001t0007g0022 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.112-49C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827952 | ||||||
chr12:65828238
|
C | T | 1 | a0001c0001t0073g0165 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.198+151C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828238 | ||||||
chr12:65828331
|
T | A | 1 | a0001c0001t0122g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.198+244T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828331 | ||||||
chr12:65828370
|
T | TG | 4 | a0001c0001t0003g0009a0001c0001t0048g0215a0001c0001t0106g0167others(1): Show | 4 | HG02683.hp1 HG03098.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+284dupG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65828370 | |||||
chr12:65828370
|
T | TGG | 4 | a0001c0001t0046g0169a0001c0001t0104g0216a0001c0001t0105g0168others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+284_198+285ins others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65828370 | |||||
chr12:65828371
|
GC | G | 7 | a0001c0001t0018g0223a0001c0001t0018g0225a0001c0001t0102g0218others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+285delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828371 | ||||||
chr12:65828372
|
C | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(115): Show | 118 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.198+285C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828372 | ||||||
chr12:65828373
|
G | GGGGC | 59 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0033others(56): Show | 59 | HG00558.hp1 HG00558.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.198+289_198+290ins others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65828373 | |||||
chr12:65828786
|
T | G | 1 | a0001c0001t0133g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.198+699T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828786 | ||||||
chr12:65828978
|
T | G | 1 | a0001c0001t0036g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.198+891T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828978 | ||||||
chr12:65829238
|
C | G | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+1151C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829238 | ||||||
chr12:65829368
|
G | A | 1 | a0001c0001t0083g0088 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.198+1281G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829368 | ||||||
chr12:65829404
|
T | A | 3 | a0001c0001t0047g0183a0001c0001t0110g0182a0001c0001t0113g0181 | 3 | HG02922.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.198+1317T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829404 | ||||||
chr12:65829525
|
T | G | 13 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+1438T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829525 | ||||||
chr12:65829766
|
T | C | 13 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+1679T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829766 | ||||||
chr12:65829938
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.198+1851C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829938 | ||||||
chr12:65829939
|
G | A | 1 | a0001c0001t0046g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.198+1852G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829939 | ||||||
chr12:65830681
|
A | C | 20 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(17): Show | 20 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.198+2594A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65830681 | ||||||
chr12:65830765
|
A | G | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+2678A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65830765 | ||||||
chr12:65830968
|
G | A | 1 | a0001c0001t0031g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.198+2881G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65830968 | ||||||
chr12:65831060
|
A | T | 1 | a0001c0001t0063g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.198+2973A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831060 | ||||||
chr12:65831186
|
C | T | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198+3099C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831186 | ||||||
chr12:65831224
|
T | A | 3 | a0001c0001t0008g0090a0001c0001t0064g0016a0001c0001t0073g0165 | 3 | HG01433.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.198+3137T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831224 | ||||||
chr12:65831408
|
G | GT | 122 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(119): Show | 122 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.198+3328dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65831408 | |||||
chr12:65831455
|
TA | T | 5 | a0001c0001t0008g0161a0001c0001t0029g0160a0001c0001t0062g0163others(2): Show | 5 | HG00735.hp2 HG01070.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+3378delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65831455 | |||||
chr12:65831458
|
A | G | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.198+3371A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831458 | ||||||
chr12:65831485
|
C | A | 3 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0049g0186 | 3 | HG02559.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.198+3398C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831485 | ||||||
chr12:65831553
|
A | G | 66 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.198+3466A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831553 | ||||||
chr12:65831749
|
C | G | 38 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0190others(35): Show | 38 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.198+3662C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831749 | ||||||
chr12:65832305
|
C | T | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.198+4218C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65832305 | ||||||
chr12:65832461
|
A | G | 8 | a0001c0001t0013g0153a0001c0001t0013g0156a0001c0001t0024g0155others(5): Show | 8 | HG00673.hp1 HG02074.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+4374A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65832461 | ||||||
chr12:65833314
|
G | A | 1 | a0001c0001t0011g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199-5205G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833314 | ||||||
chr12:65833413
|
GT | G | 133 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(130): Show | 133 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.199-5092delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65833413 | |||||
chr12:65833460
|
G | T | 1 | a0001c0001t0090g0078 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199-5059G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833460 | ||||||
chr12:65833477
|
C | T | 63 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.199-5042C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833477 | ||||||
chr12:65833531
|
C | T | 1 | a0001c0001t0074g0150 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.199-4988C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833531 | ||||||
chr12:65833544
|
C | T | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.199-4975C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833544 | ||||||
chr12:65833609
|
C | G | 63 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.199-4910C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833609 | ||||||
chr12:65833613
|
G | A | 13 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-4906G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833613 | ||||||
chr12:65833699
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0132g0028 | 2 | HG00609.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.199-4820T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833699 | ||||||
chr12:65833809
|
A | C | 2 | a0001c0001t0003g0213a0001c0001t0003g0214 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.199-4710A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833809 | ||||||
chr12:65833810
|
C | T | 1 | a0001c0001t0007g0072 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.199-4709C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833810 | ||||||
chr12:65833902
|
G | C | 2 | a0001c0001t0021g0170a0001c0001t0021g0171 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.199-4617G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833902 | ||||||
chr12:65834022
|
T | C | 2 | a0001c0001t0040g0091a0001c0001t0071g0092 | 2 | NA18951.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.199-4497T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834022 | ||||||
chr12:65834065
|
T | C | 1 | a0001c0001t0033g0093 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.199-4454T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834065 | ||||||
chr12:65834140
|
C | T | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.199-4379C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834140 | ||||||
chr12:65834148
|
C | G | 3 | a0001c0001t0107g0220a0001c0001t0116g0219a0001c0001t0122g0230 | 3 | HG01361.hp2 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.199-4371C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834148 | ||||||
chr12:65834162
|
G | A | 1 | a0001c0001t0007g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.199-4357G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834162 | ||||||
chr12:65834169
|
A | G | 1 | a0001c0001t0005g0059 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.199-4350A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834169 | ||||||
chr12:65834243
|
G | A | 3 | a0001c0001t0002g0060a0001c0001t0007g0021a0001c0001t0007g0022 | 3 | HG00733.hp1 HG01070.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.199-4276G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834243 | ||||||
chr12:65834279
|
A | C | 67 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.199-4240A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834279 | ||||||
chr12:65834312
|
T | A | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.199-4207T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834312 | ||||||
chr12:65834531
|
CTCCT | C | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.199-3982_199-3979d others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65834531 | |||||
chr12:65834887
|
G | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-3632G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834887 | ||||||
chr12:65835052
|
C | T | 1 | a0001c0001t0022g0146 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.199-3467C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65835052 | ||||||
chr12:65835628
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0132g0028 | 2 | HG00609.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.199-2891C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65835628 | ||||||
chr12:65836074
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.199-2445G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836074 | ||||||
chr12:65836142
|
G | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.199-2377G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836142 | ||||||
chr12:65836156
|
G | C | 1 | a0001c0001t0001g0029 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.199-2363G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836156 | ||||||
chr12:65836175
|
T | C | 4 | a0001c0001t0018g0013a0001c0001t0086g0217a0001c0001t0104g0216others(1): Show | 4 | HG02258.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2344T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836175 | ||||||
chr12:65836187
|
G | C | 1 | a0001c0001t0030g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-2332G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836187 | ||||||
chr12:65836228
|
A | G | 5 | a0001c0001t0002g0070a0001c0001t0004g0069a0001c0001t0007g0072others(2): Show | 5 | NA18941.hp1 NA18951.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2291A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836228 | ||||||
chr12:65836276
|
G | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-2243G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836276 | ||||||
chr12:65836304
|
A | C | 3 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008 | 3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.199-2215A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836304 | ||||||
chr12:65836364
|
GA | G | 80 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(77): Show | 80 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.199-2140delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65836364 | |||||
chr12:65836375
|
A | G | 1 | a0001c0001t0050g0145 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.199-2144A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836375 | ||||||
chr12:65836376
|
A | G | 2 | a0001c0001t0062g0163a0001c0001t0069g0144 | 2 | HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.199-2143A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836376 | ||||||
chr12:65836390
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.199-2129C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836390 | ||||||
chr12:65836686
|
G | A | 1 | a0001c0001t0028g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.199-1833G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836686 | ||||||
chr12:65836699
|
C | T | 8 | a0001c0001t0003g0009a0001c0001t0107g0220a0001c0001t0115g0007others(5): Show | 8 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-1820C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836699 | ||||||
chr12:65837196
|
T | C | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.199-1323T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837196 | ||||||
chr12:65837337
|
T | C | 1 | a0001c0001t0034g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.199-1182T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837337 | ||||||
chr12:65837344
|
C | A | 2 | a0001c0001t0004g0074a0001c0001t0015g0075 | 2 | HG02074.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.199-1175C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837344 | ||||||
chr12:65837389
|
G | C | 1 | a0001c0001t0035g0148 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.199-1130G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837389 | ||||||
chr12:65837585
|
C | T | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-934C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837585 | ||||||
chr12:65837846
|
T | C | 84 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.199-673T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837846 | ||||||
chr12:65838393
|
C | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | HG02132.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.199-126C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838393 | ||||||
chr12:65838393
|
CA | C | 85 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(82): Show | 85 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.199-113delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65838393 | |||||
chr12:65838394
|
A | C | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | HG02132.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.199-125A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838394 | ||||||
chr12:65838398
|
A | C | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-121A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838398 | ||||||
chr12:65838511
|
A | G | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.199-8A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838511 | ||||||
chr12:65838575
|
T | A | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
splice_region_variant&intron_variant | LOW | c.249+6T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838575 | ||||||
chr12:65838598
|
T | C | 13 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+29T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838598 | ||||||
chr12:65838603
|
T | TG | 38 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0190others(35): Show | 38 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.249+34_249+35insG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838603 | ||||||
chr12:65838648
|
G | A | 3 | a0001c0001t0083g0088a0001c0001t0093g0095a0001c0001t0133g0087 | 3 | HG02027.hp2 NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.249+79G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838648 | ||||||
chr12:65838962
|
C | T | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+393C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838962 | ||||||
chr12:65838985
|
TC | T | 3 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0049g0186 | 3 | HG02559.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.249+417delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838985 | ||||||
chr12:65838986
|
C | T | 1 | a0001c0001t0046g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.249+417C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838986 | ||||||
chr12:65838992
|
C | T | 4 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0046g0169others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+423C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838992 | ||||||
chr12:65838998
|
C | CT | 6 | a0001c0001t0008g0139a0001c0001t0015g0140a0001c0001t0027g0158others(3): Show | 6 | HG00621.hp2 HG02300.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+441dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65838998
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0007g0063a0001c0001t0060g0172a0001c0001t0113g0181 | 3 | HG02809.hp2 HG03209.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.249+430_249+441dup others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65838998
|
C | CTTTTTTT others(6): Show |
72 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(69): Show | 72 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.249+441_249+442ins others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65838998
|
C | CTTTTTTT others(7): Show |
15 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0068others(12): Show | 15 | HG00558.hp1 HG00558.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.249+441_249+442ins others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65838998
|
C | CTTTTTTT others(8): Show |
30 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0006g0197others(27): Show | 30 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.249+441_249+442ins others(15): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65838998
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0126g0212 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.249+441_249+442ins others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65838998
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+441_249+442ins others(20): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65838998
|
C | T | 4 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0046g0169others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+429C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838998 | ||||||
chr12:65838998
|
CT | C | 7 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0116g0219others(4): Show | 7 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+441delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | |||||
chr12:65839030
|
G | T | 126 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(123): Show | 126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.249+461G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839030 | ||||||
chr12:65839344
|
A | G | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+775A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839344 | ||||||
chr12:65839445
|
T | C | 1 | a0001c0001t0010g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.249+876T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839445 | ||||||
chr12:65839474
|
A | AT | 7 | a0001c0001t0015g0149a0001c0001t0028g0231a0001c0001t0030g0147others(4): Show | 7 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+915dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65839474 | |||||
chr12:65839637
|
G | T | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+1068G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839637 | ||||||
chr12:65839752
|
A | G | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+1183A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839752 | ||||||
chr12:65839995
|
G | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+1426G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839995 | ||||||
chr12:65840329
|
G | T | 1 | a0001c0001t0001g0054 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.249+1760G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840329 | ||||||
chr12:65840343
|
G | C | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+1774G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840343 | ||||||
chr12:65840480
|
A | G | 1 | a0001c0001t0075g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.249+1911A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840480 | ||||||
chr12:65840746
|
A | T | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+2177A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840746 | ||||||
chr12:65840747
|
T | A | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+2178T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840747 | ||||||
chr12:65840937
|
G | A | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+2368G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840937 | ||||||
chr12:65840977
|
C | G | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+2408C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840977 | ||||||
chr12:65840978
|
G | A | 84 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.249+2409G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840978 | ||||||
chr12:65841008
|
C | A | 1 | a0001c0001t0033g0096 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.249+2439C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841008 | ||||||
chr12:65841663
|
C | T | 1 | a0001c0001t0018g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+3094C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841663 | ||||||
chr12:65841684
|
T | C | 37 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0190others(34): Show | 37 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+3115T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841684 | ||||||
chr12:65841961
|
A | G | 2 | a0001c0001t0118g0232a0001c0001t0128g0189 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.249+3392A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841961 | ||||||
chr12:65842220
|
G | T | 1 | a0001c0001t0087g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.249+3651G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842220 | ||||||
chr12:65842328
|
T | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+3759T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842328 | ||||||
chr12:65842533
|
G | A | 1 | a0001c0001t0004g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.249+3964G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842533 | ||||||
chr12:65842650
|
G | A | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+4081G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842650 | ||||||
chr12:65842651
|
T | G | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+4082T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842651 | ||||||
chr12:65842663
|
G | C | 1 | a0001c0001t0004g0025 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.249+4094G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842663 | ||||||
chr12:65842763
|
T | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+4194T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842763 | ||||||
chr12:65842794
|
T | A | 1 | a0001c0001t0131g0222 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.249+4225T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842794 | ||||||
chr12:65842955
|
T | C | 84 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(81): Show | 84 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.249+4386T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842955 | ||||||
chr12:65843009
|
T | A | 1 | a0001c0001t0007g0072 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.249+4440T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843009 | ||||||
chr12:65843369
|
G | A | 1 | a0001c0001t0008g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+4800G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843369 | ||||||
chr12:65843380
|
A | T | 2 | a0001c0001t0118g0232a0001c0001t0128g0189 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.249+4811A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843380 | ||||||
chr12:65843630
|
T | A | 37 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0190others(34): Show | 37 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+5061T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843630 | ||||||
chr12:65843665
|
T | TAC | 20 | a0001c0001t0030g0136a0001c0001t0033g0096a0001c0001t0046g0169others(17): Show | 20 | HG01361.hp2 HG02027.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+5128_249+5129d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | |||||
chr12:65843665
|
TAC | T | 67 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0190others(64): Show | 67 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.249+5128_249+5129d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | |||||
chr12:65843665
|
TACAC | T | 22 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(19): Show | 22 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.249+5126_249+5129d others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | |||||
chr12:65843665
|
TACACAC | T | 28 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(25): Show | 28 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.249+5124_249+5129d others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | |||||
chr12:65843682
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+5123_249+5124i others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843682 | |||||
chr12:65844026
|
G | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+5457G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844026 | ||||||
chr12:65844050
|
C | CA | 26 | a0001c0001t0003g0009a0001c0001t0006g0003a0001c0001t0006g0004others(23): Show | 26 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+5500dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65844050 | |||||
chr12:65844050
|
C | CAA | 12 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0035g0229others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+5499_249+5500d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65844050 | |||||
chr12:65844050
|
CA | C | 101 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(98): Show | 101 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.249+5500delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65844050 | |||||
chr12:65844069
|
A | G | 6 | a0001c0001t0003g0208a0001c0001t0019g0207a0001c0001t0019g0209others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+5500A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844069 | ||||||
chr12:65844407
|
T | A | 1 | a0001c0001t0003g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+5838T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844407 | ||||||
chr12:65844473
|
C | G | 2 | a0001c0001t0007g0021a0001c0001t0007g0022 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+5904C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844473 | ||||||
chr12:65844935
|
A | C | 1 | a0001c0001t0127g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.249+6366A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844935 | ||||||
chr12:65845037
|
T | A | 1 | a0001c0001t0090g0078 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.249+6468T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845037 | ||||||
chr12:65845044
|
A | G | 3 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0049g0186 | 3 | HG02559.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.249+6475A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845044 | ||||||
chr12:65845195
|
T | C | 1 | a0001c0001t0058g0152 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.249+6626T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845195 | ||||||
chr12:65845272
|
C | T | 37 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0190others(34): Show | 37 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+6703C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845272 | ||||||
chr12:65845284
|
T | A | 2 | a0001c0001t0037g0141a0001c0001t0087g0086 | 2 | HG02300.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.249+6715T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845284 | ||||||
chr12:65845331
|
A | C | 127 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(124): Show | 127 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.249+6762A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845331 | ||||||
chr12:65845499
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.249+6930C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845499 | ||||||
chr12:65845505
|
G | A | 86 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(83): Show | 86 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.249+6936G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845505 | ||||||
chr12:65845538
|
G | A | 1 | a0001c0001t0007g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.249+6969G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845538 | ||||||
chr12:65845554
|
TCAC | T | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+6989_249+6991d others(5): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65845554 | |||||
chr12:65845575
|
A | AT | 59 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(56): Show | 59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.249+7014dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65845575 | |||||
chr12:65845583
|
T | A | 2 | a0001c0001t0020g0100a0001c0001t0093g0095 | 2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.249+7014T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845583 | ||||||
chr12:65845584
|
A | T | 1 | a0001c0001t0118g0232 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.249+7015A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845584 | ||||||
chr12:65845754
|
C | T | 7 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(4): Show | 7 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+7185C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845754 | ||||||
chr12:65845793
|
C | G | 1 | a0001c0001t0018g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+7224C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845793 | ||||||
chr12:65845861
|
G | C | 85 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(82): Show | 85 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.249+7292G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845861 | ||||||
chr12:65845937
|
C | G | 126 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(123): Show | 126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.249+7368C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845937 | ||||||
chr12:65845944
|
C | G | 3 | a0001c0001t0002g0073a0001c0001t0004g0076a0001c0001t0005g0053 | 3 | HG02451.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.249+7375C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845944 | ||||||
chr12:65845982
|
C | T | 8 | a0001c0001t0003g0009a0001c0001t0107g0220a0001c0001t0115g0007others(5): Show | 8 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+7413C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845982 | ||||||
chr12:65846090
|
C | T | 85 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(82): Show | 85 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.249+7521C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846090 | ||||||
chr12:65846094
|
A | G | 88 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(85): Show | 88 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.249+7525A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846094 | ||||||
chr12:65846105
|
C | A | 63 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+7536C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846105 | ||||||
chr12:65846275
|
C | T | 1 | a0001c0001t0114g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.249+7706C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846275 | ||||||
chr12:65846352
|
T | C | 1 | a0001c0001t0028g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.249+7783T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846352 | ||||||
chr12:65846562
|
G | A | 3 | a0001c0001t0045g0050a0001c0001t0045g0055a0001c0001t0080g0048 | 3 | HG02647.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.249+7993G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846562 | ||||||
chr12:65846809
|
G | A | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+8240G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846809 | ||||||
chr12:65846994
|
T | C | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+8425T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846994 | ||||||
chr12:65847311
|
G | A | 1 | a0001c0001t0115g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249+8742G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847311 | ||||||
chr12:65847406
|
C | T | 1 | a0001c0001t0018g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+8837C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847406 | ||||||
chr12:65847592
|
C | T | 36 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0190others(33): Show | 36 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.249+9023C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847592 | ||||||
chr12:65847997
|
A | G | 24 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(21): Show | 24 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.249+9428A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847997 | ||||||
chr12:65848118
|
G | A | 91 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(88): Show | 91 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+9549G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848118 | ||||||
chr12:65848315
|
T | C | 1 | a0001c0001t0061g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.249+9746T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848315 | ||||||
chr12:65848357
|
G | A | 1 | a0001c0001t0088g0133 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.249+9788G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848357 | ||||||
chr12:65848547
|
A | G | 64 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(61): Show | 64 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.249+9978A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848547 | ||||||
chr12:65848548
|
G | A | 14 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(11): Show | 14 | HG01243.hp1 HG01361.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+9979G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848548 | ||||||
chr12:65848771
|
G | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+10202G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848771 | ||||||
chr12:65848831
|
C | T | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+10262C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848831 | ||||||
chr12:65848832
|
C | G | 1 | a0001c0001t0085g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.249+10263C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848832 | ||||||
chr12:65848842
|
G | C | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+10273G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848842 | ||||||
chr12:65848858
|
G | A | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+10289G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848858 | ||||||
chr12:65849130
|
G | A | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+10561G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849130 | ||||||
chr12:65849555
|
C | T | 1 | a0001c0001t0008g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+10986C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849555 | ||||||
chr12:65849722
|
A | G | 35 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0208others(32): Show | 35 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.249+11153A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849722 | ||||||
chr12:65849736
|
A | AT | 16 | a0001c0001t0009g0085a0001c0001t0012g0130a0001c0001t0012g0131others(13): Show | 16 | HG00423.hp1 HG00733.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+11191dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT | 22 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0065others(19): Show | 22 | HG00733.hp1 HG01070.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.249+11185_249+1119 others(11): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT others(1): Show |
19 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0033others(16): Show | 19 | HG00609.hp1 HG01192.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+11184_249+1119 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT others(2): Show |
16 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 16 | HG00558.hp1 HG01074.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+11183_249+1119 others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0010g0044others(1): Show | 4 | HG02738.hp2 HG04115.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+11182_249+1119 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+11180_249+1119 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT others(12): Show |
3 | a0001c0001t0047g0183a0001c0001t0110g0182a0001c0001t0113g0181 | 3 | HG02922.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.249+11173_249+1119 others(23): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0047g0185a0001c0001t0108g0180 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+11172_249+1119 others(24): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0102g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.249+11170_249+1119 others(26): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
AT | A | 12 | a0001c0001t0003g0190a0001c0001t0006g0004a0001c0001t0018g0225others(9): Show | 12 | HG00423.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+11191delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849736
|
ATT | A | 39 | a0001c0001t0003g0009a0001c0001t0003g0187a0001c0001t0003g0188others(36): Show | 39 | HG00609.hp2 HG00621.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.249+11190_249+1119 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | |||||
chr12:65849781
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+11212C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849781 | ||||||
chr12:65849808
|
TC | T | 14 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(11): Show | 14 | HG01243.hp1 HG01361.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+11242delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849808 | |||||
chr12:65849839
|
C | T | 1 | a0001c0001t0047g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.249+11270C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849839 | ||||||
chr12:65849984
|
G | T | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+11415G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849984 | ||||||
chr12:65850221
|
G | A | 6 | a0001c0001t0008g0080a0001c0001t0029g0082a0001c0001t0036g0077others(3): Show | 6 | HG01074.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+11652G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850221 | ||||||
chr12:65850221
|
G | T | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+11652G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850221 | ||||||
chr12:65850434
|
T | C | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+11865T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850434 | ||||||
chr12:65850512
|
G | A | 2 | a0001c0001t0107g0220a0001c0001t0122g0230 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.249+11943G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850512 | ||||||
chr12:65850515
|
T | A | 1 | a0001c0001t0018g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.249+11946T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850515 | ||||||
chr12:65850733
|
G | C | 1 | a0001c0001t0049g0191 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.249+12164G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850733 | ||||||
chr12:65851032
|
T | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+12463T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851032 | ||||||
chr12:65851256
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.249+12687G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851256 | ||||||
chr12:65851383
|
C | T | 3 | a0001c0001t0006g0204a0001c0001t0029g0082a0001c0001t0049g0191 | 3 | HG01891.hp2 NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.249+12814C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851383 | ||||||
chr12:65851421
|
C | T | 1 | a0001c0001t0055g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.249+12852C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851421 | ||||||
chr12:65851646
|
C | T | 6 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0102g0218others(3): Show | 6 | HG02451.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+13077C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851646 | ||||||
chr12:65851788
|
C | T | 27 | a0001c0001t0018g0013a0001c0001t0021g0170a0001c0001t0021g0171others(24): Show | 27 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+13219C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851788 | ||||||
chr12:65851808
|
A | G | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+13239A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851808 | ||||||
chr12:65852003
|
G | C | 1 | a0001c0001t0003g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.249+13434G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852003 | ||||||
chr12:65852017
|
C | A | 1 | a0001c0001t0111g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.249+13448C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852017 | ||||||
chr12:65852120
|
G | A | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+13551G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852120 | ||||||
chr12:65852122
|
GCAAATAA others(6): Show |
G | 10 | a0001c0001t0008g0161a0001c0001t0029g0160a0001c0001t0047g0183others(7): Show | 10 | HG00735.hp2 HG01070.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+13574_249+1358 others(17): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65852122 | |||||
chr12:65852234
|
C | T | 2 | a0001c0001t0021g0170a0001c0001t0021g0171 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.249+13665C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852234 | ||||||
chr12:65852401
|
A | G | 142 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(139): Show | 142 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.249+13832A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852401 | ||||||
chr12:65852464
|
C | T | 15 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(12): Show | 15 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.249+13895C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852464 | ||||||
chr12:65852535
|
T | C | 1 | a0001c0001t0059g0128 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.249+13966T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852535 | ||||||
chr12:65852629
|
T | C | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+14060T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852629 | ||||||
chr12:65852674
|
T | C | 9 | a0001c0001t0013g0153a0001c0001t0013g0156a0001c0001t0024g0155others(6): Show | 9 | HG00673.hp1 HG02074.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+14105T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852674 | ||||||
chr12:65853017
|
A | G | 22 | a0001c0001t0018g0013a0001c0001t0021g0170a0001c0001t0021g0171others(19): Show | 22 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.249+14448A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853017 | ||||||
chr12:65853088
|
G | A | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+14519G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853088 | ||||||
chr12:65853108
|
G | A | 22 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(19): Show | 22 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.249+14539G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853108 | ||||||
chr12:65853120
|
G | A | 3 | a0001c0001t0008g0090a0001c0001t0064g0016a0001c0001t0073g0165 | 3 | HG01433.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.249+14551G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853120 | ||||||
chr12:65853230
|
C | G | 80 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(77): Show | 80 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.249+14661C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853230 | ||||||
chr12:65853271
|
C | T | 91 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(88): Show | 91 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+14702C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853271 | ||||||
chr12:65853464
|
T | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+14895T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853464 | ||||||
chr12:65853477
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0004 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.249+14908G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853477 | ||||||
chr12:65853660
|
G | A | 1 | a0001c0001t0012g0130 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.249+15091G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853660 | ||||||
chr12:65853711
|
G | T | 1 | a0001c0001t0008g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+15142G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853711 | ||||||
chr12:65853819
|
A | G | 17 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(14): Show | 17 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+15250A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853819 | ||||||
chr12:65854308
|
C | T | 1 | a0001c0001t0039g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.249+15739C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854308 | ||||||
chr12:65854438
|
T | C | 21 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(18): Show | 21 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+15869T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854438 | ||||||
chr12:65854543
|
C | T | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+15974C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854543 | ||||||
chr12:65854819
|
A | T | 1 | a0001c0001t0033g0096 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.249+16250A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854819 | ||||||
chr12:65854874
|
C | A | 1 | a0001c0001t0018g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+16305C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854874 | ||||||
chr12:65855400
|
A | G | 1 | a0001c0001t0023g0132 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.249+16831A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855400 | ||||||
chr12:65855448
|
T | TCA | 4 | a0001c0001t0018g0223a0001c0001t0018g0225a0001c0001t0098g0030others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+16880_249+1688 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855448 | |||||
chr12:65855450
|
T | A | 4 | a0001c0001t0018g0223a0001c0001t0018g0225a0001c0001t0098g0030others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+16881T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855450 | ||||||
chr12:65855450
|
T | TCA | 7 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(4): Show | 7 | HG01884.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+16882_249+1688 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855450 | |||||
chr12:65855452
|
T | A | 14 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(11): Show | 14 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+16883T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855452 | ||||||
chr12:65855452
|
T | TCA | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+16884_249+1688 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855452 | |||||
chr12:65855454
|
T | A | 17 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(14): Show | 17 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+16885T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855454 | ||||||
chr12:65855456
|
T | A | 17 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(14): Show | 17 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+16887T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855456 | ||||||
chr12:65855458
|
T | A | 18 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(15): Show | 18 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.249+16889T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855458 | ||||||
chr12:65855458
|
T | TCA | 12 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0004g0038others(9): Show | 12 | HG00673.hp2 HG02630.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+16920_249+1692 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
T | TCACA | 94 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(91): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.249+16918_249+1692 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
T | TCACACA | 38 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(35): Show | 38 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.249+16916_249+1692 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
T | TCACACAC others(1): Show |
8 | a0001c0001t0001g0033a0001c0001t0002g0073a0001c0001t0004g0074others(5): Show | 8 | HG02074.hp1 HG02165.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+16914_249+1692 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
T | TCTCA | 3 | a0001c0001t0034g0126a0001c0001t0093g0095a0001c0001t0116g0219 | 3 | HG01361.hp2 NA18994.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.249+16890_249+1689 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
T | TCTCACA | 9 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0021g0171others(6): Show | 9 | HG02257.hp2 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+16890_249+1689 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
T | TCTCACAC others(1): Show |
8 | a0001c0001t0007g0021a0001c0001t0007g0022a0001c0001t0021g0170others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+16890_249+1689 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
T | TCTCTCAC others(5): Show |
1 | a0001c0001t0060g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+16890_249+1689 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855458
|
TCA | T | 4 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+16920_249+1692 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | |||||
chr12:65855460
|
A | T | 1 | a0001c0001t0003g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+16891A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855460 | ||||||
chr12:65855462
|
A | T | 3 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008 | 3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+16893A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855462 | ||||||
chr12:65855565
|
G | A | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+16996G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855565 | ||||||
chr12:65855687
|
T | C | 1 | a0001c0001t0053g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.249+17118T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855687 | ||||||
chr12:65855699
|
A | AGAT | 103 | a0001c0001t0001g0029a0001c0001t0002g0060a0001c0001t0002g0061others(100): Show | 103 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.249+17167_249+1716 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855699 | |||||
chr12:65855699
|
A | AGATGAT | 62 | a0001c0001t0008g0080a0001c0001t0008g0139a0001c0001t0009g0085others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.249+17164_249+1716 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855699 | |||||
chr12:65855699
|
A | AGATGATG others(2): Show |
13 | a0001c0001t0008g0161a0001c0001t0046g0169a0001c0001t0047g0183others(10): Show | 13 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+17161_249+1716 others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855699 | |||||
chr12:65855716
|
A | G | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+17147A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855716 | ||||||
chr12:65855801
|
T | C | 63 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+17232T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855801 | ||||||
chr12:65855825
|
G | T | 63 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+17256G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855825 | ||||||
chr12:65855888
|
C | CT | 20 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(17): Show | 20 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+17332dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855888 | |||||
chr12:65855942
|
G | A | 3 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008 | 3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+17373G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855942 | ||||||
chr12:65855992
|
A | G | 2 | a0001c0001t0007g0063a0001c0001t0043g0026 | 2 | NA18942.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.249+17423A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855992 | ||||||
chr12:65856157
|
A | T | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+17588A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856157 | ||||||
chr12:65856181
|
G | A | 2 | a0001c0001t0007g0021a0001c0001t0007g0022 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+17612G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856181 | ||||||
chr12:65856288
|
G | C | 2 | a0001c0001t0007g0021a0001c0001t0007g0022 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+17719G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856288 | ||||||
chr12:65856312
|
A | G | 4 | a0001c0001t0046g0169a0001c0001t0104g0216a0001c0001t0105g0168others(1): Show | 4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+17743A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856312 | ||||||
chr12:65856684
|
G | A | 1 | a0001c0001t0101g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249+18115G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856684 | ||||||
chr12:65856793
|
C | T | 2 | a0001c0001t0007g0021a0001c0001t0007g0022 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+18224C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856793 | ||||||
chr12:65857160
|
T | G | 92 | a0001c0001t0008g0080a0001c0001t0008g0090a0001c0001t0008g0139others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.249+18591T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65857160 | ||||||
chr12:65857375
|
T | C | 4 | a0001c0001t0046g0169a0001c0001t0104g0216a0001c0001t0105g0168others(1): Show | 4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+18806T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65857375 | ||||||
chr12:65857755
|
A | T | 1 | a0001c0001t0118g0232 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.249+19186A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65857755 | ||||||
chr12:65858347
|
A | G | 1 | a0001c0001t0059g0128 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.249+19778A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65858347 | ||||||
chr12:65858514
|
A | G | 114 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0008g0080others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.249+19945A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65858514 | ||||||
chr12:65858847
|
A | G | 1 | a0001c0001t0055g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.249+20278A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65858847 | ||||||
chr12:65859081
|
G | A | 21 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.249+20512G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859081 | ||||||
chr12:65859173
|
C | T | 1 | a0001c0001t0010g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.249+20604C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859173 | ||||||
chr12:65859374
|
A | T | 1 | a0001c0001t0016g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249+20805A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859374 | ||||||
chr12:65859713
|
G | A | 23 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(20): Show | 23 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.249+21144G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859713 | ||||||
chr12:65859807
|
T | A | 7 | a0001c0001t0009g0001a0001c0001t0017g0194a0001c0001t0038g0193others(4): Show | 7 | HG00609.hp2 HG00621.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+21238T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859807 | ||||||
chr12:65859918
|
T | TA | 21 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(18): Show | 21 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+21365dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65859918 | |||||
chr12:65860239
|
G | A | 2 | a0001c0001t0015g0149a0001c0001t0129g0196 | 2 | HG00140.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.249+21670G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860239 | ||||||
chr12:65860448
|
A | G | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+21879A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860448 | ||||||
chr12:65860599
|
C | T | 1 | a0001c0001t0020g0100 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.249+22030C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860599 | ||||||
chr12:65860745
|
T | G | 1 | a0001c0001t0122g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.249+22176T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860745 | ||||||
chr12:65861021
|
T | C | 1 | a0001c0001t0080g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.249+22452T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861021 | ||||||
chr12:65861089
|
C | G | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+22520C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861089 | ||||||
chr12:65861150
|
G | A | 78 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(75): Show | 78 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.249+22581G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861150 | ||||||
chr12:65861199
|
C | G | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+22630C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861199 | ||||||
chr12:65861223
|
G | A | 78 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(75): Show | 78 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.249+22654G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861223 | ||||||
chr12:65861225
|
G | C | 95 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0008g0080others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.249+22656G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861225 | ||||||
chr12:65861364
|
T | TCAAAA | 2 | a0001c0001t0002g0039a0001c0001t0064g0016 | 2 | HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.249+22821_249+2282 others(9): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861364 | |||||
chr12:65861370
|
C | G | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+22801C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861370 | ||||||
chr12:65861469
|
G | A | 1 | a0001c0001t0016g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249+22900G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861469 | ||||||
chr12:65861623
|
T | TA | 79 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(76): Show | 79 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.249+23072dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861623 | |||||
chr12:65861623
|
T | TAA | 8 | a0001c0001t0010g0031a0001c0001t0015g0075a0001c0001t0045g0050others(5): Show | 8 | HG01192.hp2 HG02074.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+23071_249+2307 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861623 | |||||
chr12:65861680
|
T | C | 2 | a0001c0001t0035g0229a0001c0001t0116g0219 | 2 | HG01361.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.249+23111T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861680 | ||||||
chr12:65861733
|
T | TATTTATT others(5): Show |
1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23165_249+2316 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861733 | |||||
chr12:65861735
|
G | A | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23166G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861735 | ||||||
chr12:65861736
|
A | T | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23167A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861736 | ||||||
chr12:65861740
|
T | C | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23171T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861740 | ||||||
chr12:65861741
|
A | T | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23172A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861741 | ||||||
chr12:65861748
|
T | A | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23179T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861748 | ||||||
chr12:65861752
|
T | TATCTAGT others(3): Show |
1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23183_249+2318 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861752 | ||||||
chr12:65861772
|
T | C | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23203T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861772 | ||||||
chr12:65861780
|
T | G | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23211T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861780 | ||||||
chr12:65861782
|
T | C | 1 | a0001c0001t0015g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.249+23213T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861782 | ||||||
chr12:65861790
|
C | T | 11 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0035g0229others(8): Show | 11 | HG01361.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+23221C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861790 | ||||||
chr12:65861794
|
T | A | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23225T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861794 | ||||||
chr12:65861806
|
A | C | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23237A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861806 | ||||||
chr12:65861810
|
T | A | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23241T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861810 | ||||||
chr12:65861811
|
T | G | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23242T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861811 | ||||||
chr12:65861827
|
G | A | 1 | a0001c0001t0057g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.249+23258G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861827 | ||||||
chr12:65861828
|
T | G | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23259T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861828 | ||||||
chr12:65861833
|
G | C | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23264G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861833 | ||||||
chr12:65861835
|
G | A | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23266G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861835 | ||||||
chr12:65861846
|
C | CT | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(2): Show | 5 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+23292dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861846 | |||||
chr12:65861846
|
C | T | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23277C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861846 | ||||||
chr12:65861849
|
T | C | 1 | a0001c0001t0027g0157 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23280T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861849 | ||||||
chr12:65861855
|
T | C | 1 | a0001c0001t0009g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.249+23286T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861855 | ||||||
chr12:65861856
|
T | C | 2 | a0001c0001t0035g0229a0001c0001t0116g0219 | 2 | HG01361.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.249+23287T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861856 | ||||||
chr12:65861874
|
C | T | 1 | a0001c0001t0060g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+23305C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861874 | ||||||
chr12:65862017
|
G | A | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+23448G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862017 | ||||||
chr12:65862097
|
G | T | 1 | a0001c0001t0121g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.249+23528G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862097 | ||||||
chr12:65862127
|
G | A | 1 | a0001c0001t0037g0141 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.249+23558G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862127 | ||||||
chr12:65862276
|
T | TAC | 94 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0008g0080others(91): Show | 94 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.249+23737_249+2373 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | |||||
chr12:65862276
|
T | TACAC | 57 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.249+23735_249+2373 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | |||||
chr12:65862276
|
T | TACACAC | 11 | a0001c0001t0001g0046a0001c0001t0002g0061a0001c0001t0002g0062others(8): Show | 11 | HG01891.hp1 HG02040.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+23733_249+2373 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | |||||
chr12:65862276
|
T | TACACACA others(3): Show |
7 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(4): Show | 7 | HG01884.hp2 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+23729_249+2373 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | |||||
chr12:65862276
|
T | TACACACA others(7): Show |
1 | a0001c0001t0018g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.249+23725_249+2373 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | |||||
chr12:65862276
|
TAC | T | 2 | a0001c0001t0014g0159a0001c0001t0027g0157 | 2 | NA18991.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.249+23737_249+2373 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | |||||
chr12:65862296
|
C | CACAT | 11 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0035g0229others(8): Show | 11 | HG01361.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+23730_249+2373 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862296 | |||||
chr12:65862374
|
A | C | 1 | a0001c0001t0111g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.249+23805A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862374 | ||||||
chr12:65862457
|
A | G | 1 | a0001c0001t0040g0091 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.249+23888A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862457 | ||||||
chr12:65862615
|
G | C | 100 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(97): Show | 100 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.249+24046G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862615 | ||||||
chr12:65862708
|
T | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+24139T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862708 | ||||||
chr12:65862764
|
G | A | 4 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0040g0091others(1): Show | 4 | NA18951.hp2 NA18953.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+24195G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862764 | ||||||
chr12:65862921
|
A | G | 4 | a0001c0001t0046g0169a0001c0001t0104g0216a0001c0001t0105g0168others(1): Show | 4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+24352A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862921 | ||||||
chr12:65863105
|
C | T | 1 | a0001c0001t0091g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.249+24536C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65863105 | ||||||
chr12:65863167
|
A | C | 64 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(61): Show | 64 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.249+24598A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65863167 | ||||||
chr12:65863447
|
GTCCTGGT | G | 5 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0035g0229others(2): Show | 5 | HG01361.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+24882_249+2488 others(11): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65863447 | |||||
chr12:65863575
|
GA | G | 27 | a0001c0001t0008g0090a0001c0001t0012g0111a0001c0001t0012g0130others(24): Show | 27 | HG00733.hp2 HG01167.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.249+25015delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65863575 | |||||
chr12:65864456
|
C | G | 99 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(96): Show | 99 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.249+25887C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864456 | ||||||
chr12:65864515
|
G | T | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+25946G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864515 | ||||||
chr12:65864715
|
T | C | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+26146T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864715 | ||||||
chr12:65864925
|
A | G | 2 | a0001c0001t0004g0058a0001c0001t0010g0057 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.249+26356A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864925 | ||||||
chr12:65864997
|
C | T | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+26428C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864997 | ||||||
chr12:65865042
|
C | T | 66 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(63): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.249+26473C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865042 | ||||||
chr12:65865119
|
C | T | 2 | a0001c0001t0035g0229a0001c0001t0116g0219 | 2 | HG01361.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.249+26550C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865119 | ||||||
chr12:65865150
|
T | C | 2 | a0001c0001t0030g0136a0001c0001t0066g0135 | 2 | HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.249+26581T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865150 | ||||||
chr12:65865192
|
G | T | 200 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.249+26623G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865192 | ||||||
chr12:65865276
|
G | A | 4 | a0001c0001t0046g0169a0001c0001t0104g0216a0001c0001t0105g0168others(1): Show | 4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+26707G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865276 | ||||||
chr12:65865336
|
G | C | 200 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.249+26767G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865336 | ||||||
chr12:65865633
|
C | CT | 9 | a0001c0001t0004g0025a0001c0001t0008g0139a0001c0001t0030g0147others(6): Show | 9 | HG00621.hp1 HG02083.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+27083dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65865633 | |||||
chr12:65865690
|
A | G | 1 | a0001c0001t0093g0095 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.249+27121A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865690 | ||||||
chr12:65865884
|
T | C | 201 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.249+27315T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865884 | ||||||
chr12:65865885
|
G | A | 6 | a0001c0001t0030g0136a0001c0001t0033g0096a0001c0001t0036g0098others(3): Show | 6 | HG02027.hp2 HG02135.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+27316G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865885 | ||||||
chr12:65865933
|
C | T | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+27364C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865933 | ||||||
chr12:65865949
|
T | A | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+27380T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865949 | ||||||
chr12:65865949
|
TC | T | 4 | a0001c0001t0046g0169a0001c0001t0104g0216a0001c0001t0105g0168others(1): Show | 4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+27381delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865949 | ||||||
chr12:65866294
|
A | T | 20 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.249+27725A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866294 | ||||||
chr12:65866430
|
A | G | 1 | a0001c0001t0074g0150 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.249+27861A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866430 | ||||||
chr12:65866516
|
T | G | 1 | a0001c0001t0016g0113 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.249+27947T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866516 | ||||||
chr12:65866778
|
TA | T | 7 | a0001c0001t0007g0017a0001c0001t0035g0229a0001c0001t0043g0018others(4): Show | 7 | HG01074.hp2 HG01361.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+28220delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65866778 | |||||
chr12:65866885
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+28316G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866885 | ||||||
chr12:65866936
|
G | A | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+28367G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866936 | ||||||
chr12:65866953
|
C | A | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+28384C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866953 | ||||||
chr12:65867003
|
A | T | 3 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0042g0047 | 3 | HG02818.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.249+28434A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867003 | ||||||
chr12:65867034
|
A | G | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+28465A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867034 | ||||||
chr12:65867144
|
A | G | 96 | a0001c0001t0001g0029a0001c0001t0006g0197a0001c0001t0006g0198others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.249+28575A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867144 | ||||||
chr12:65867145
|
C | G | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+28576C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867145 | ||||||
chr12:65867211
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+28642C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867211 | ||||||
chr12:65867226
|
T | A | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+28657T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867226 | ||||||
chr12:65867993
|
C | T | 6 | a0001c0001t0008g0080a0001c0001t0029g0082a0001c0001t0036g0077others(3): Show | 6 | HG01074.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+29424C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867993 | ||||||
chr12:65868197
|
A | G | 96 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(93): Show | 96 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.249+29628A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868197 | ||||||
chr12:65868287
|
G | A | 1 | a0001c0001t0015g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.249+29718G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868287 | ||||||
chr12:65868618
|
G | A | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+30049G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868618 | ||||||
chr12:65868911
|
G | A | 2 | a0001c0001t0018g0013a0001c0001t0109g0012 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+30342G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868911 | ||||||
chr12:65868961
|
G | A | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+30392G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868961 | ||||||
chr12:65868978
|
G | A | 3 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008 | 3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+30409G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868978 | ||||||
chr12:65869170
|
G | C | 5 | a0001c0001t0046g0169a0001c0001t0104g0216a0001c0001t0105g0168others(2): Show | 5 | HG02257.hp1 HG02683.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+30601G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869170 | ||||||
chr12:65869208
|
A | T | 200 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.249+30639A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869208 | ||||||
chr12:65869253
|
T | C | 1 | a0001c0001t0028g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.249+30684T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869253 | ||||||
chr12:65869328
|
T | C | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+30759T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869328 | ||||||
chr12:65869420
|
C | T | 1 | a0001c0001t0007g0072 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.249+30851C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869420 | ||||||
chr12:65869542
|
T | C | 1 | a0001c0001t0093g0095 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.249+30973T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869542 | ||||||
chr12:65869795
|
A | G | 1 | a0001c0001t0102g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.249+31226A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869795 | ||||||
chr12:65870120
|
G | A | 1 | a0001c0001t0004g0069 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.249+31551G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870120 | ||||||
chr12:65870211
|
C | T | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+31642C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870211 | ||||||
chr12:65870222
|
G | A | 1 | a0001c0001t0023g0132 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.249+31653G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870222 | ||||||
chr12:65870276
|
C | G | 6 | a0001c0001t0051g0176a0001c0001t0052g0178a0001c0001t0053g0010others(3): Show | 6 | HG02257.hp2 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+31707C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870276 | ||||||
chr12:65870426
|
T | C | 20 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0013others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.249+31857T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870426 | ||||||
chr12:65870530
|
A | G | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+31961A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870530 | ||||||
chr12:65870616
|
G | C | 1 | a0001c0001t0075g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.249+32047G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870616 | ||||||
chr12:65870742
|
A | G | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+32173A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870742 | ||||||
chr12:65870976
|
A | G | 2 | a0001c0001t0107g0220a0001c0001t0122g0230 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.249+32407A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870976 | ||||||
chr12:65871165
|
T | C | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+32596T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871165 | ||||||
chr12:65871230
|
G | A | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+32661G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871230 | ||||||
chr12:65871262
|
C | T | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+32693C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871262 | ||||||
chr12:65871300
|
C | T | 1 | a0001c0001t0042g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.249+32731C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871300 | ||||||
chr12:65871338
|
C | T | 6 | a0001c0001t0008g0161a0001c0001t0029g0160a0001c0001t0062g0163others(3): Show | 6 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+32769C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871338 | ||||||
chr12:65871534
|
G | T | 2 | a0001c0001t0005g0064a0001c0001t0100g0020 | 2 | NA18972.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.249+32965G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871534 | ||||||
chr12:65871637
|
T | C | 63 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(60): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+33068T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871637 | ||||||
chr12:65871901
|
G | A | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+33332G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871901 | ||||||
chr12:65872274
|
T | C | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+33705T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872274 | ||||||
chr12:65872353
|
G | A | 2 | a0001c0001t0004g0058a0001c0001t0010g0057 | 2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.249+33784G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872353 | ||||||
chr12:65872394
|
G | A | 1 | a0001c0001t0070g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.249+33825G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872394 | ||||||
chr12:65872504
|
G | A | 7 | a0001c0001t0018g0013a0001c0001t0047g0183a0001c0001t0047g0185others(4): Show | 7 | HG02922.hp2 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+33935G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872504 | ||||||
chr12:65872613
|
A | G | 58 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(55): Show | 58 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.249+34044A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872613 | ||||||
chr12:65872740
|
T | G | 3 | a0001c0001t0016g0113a0001c0001t0031g0089a0001c0001t0096g0234 | 3 | HG00280.hp1 NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.249+34171T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872740 | ||||||
chr12:65872787
|
A | G | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+34218A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872787 | ||||||
chr12:65872837
|
G | A | 1 | a0001c0001t0113g0181 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.249+34268G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872837 | ||||||
chr12:65872941
|
C | T | 9 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+34372C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872941 | ||||||
chr12:65873198
|
C | T | 3 | a0001c0001t0007g0017a0001c0001t0043g0018a0001c0001t0103g0019 | 3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.249+34629C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873198 | ||||||
chr12:65873356
|
G | A | 11 | a0001c0001t0002g0073a0001c0001t0003g0009a0001c0001t0004g0076others(8): Show | 11 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+34787G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873356 | ||||||
chr12:65873596
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.249+35027G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873596 | ||||||
chr12:65873692
|
A | G | 1 | a0001c0001t0131g0222 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.249+35123A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873692 | ||||||
chr12:65873923
|
GTAGGTAA others(5): Show |
G | 1 | a0001c0001t0134g0114 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.249+35359_249+3537 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65873923 | |||||
chr12:65873939
|
G | A | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249+35370G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873939 | ||||||
chr12:65874159
|
C | T | 1 | a0001c0001t0129g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.249+35590C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874159 | ||||||
chr12:65874189
|
C | T | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+35620C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874189 | ||||||
chr12:65874325
|
C | G | 1 | a0001c0001t0036g0098 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.249+35756C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874325 | ||||||
chr12:65874451
|
G | A | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249+35882G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874451 | ||||||
chr12:65874968
|
C | G | 1 | a0001c0001t0014g0112 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.249+36399C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874968 | ||||||
chr12:65875002
|
C | G | 57 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.249+36433C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875002 | ||||||
chr12:65875011
|
C | T | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+36442C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875011 | ||||||
chr12:65875110
|
T | TA | 70 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 70 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.249+36542dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875110 | |||||
chr12:65875112
|
T | A | 70 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(67): Show | 70 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.249+36543T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875112 | ||||||
chr12:65875187
|
A | G | 1 | a0001c0001t0120g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.249+36618A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875187 | ||||||
chr12:65875188
|
T | C | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+36619T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875188 | ||||||
chr12:65875589
|
A | AT | 9 | a0001c0001t0003g0214a0001c0001t0017g0194a0001c0001t0019g0207others(6): Show | 9 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+37061dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(3): Show |
9 | a0001c0001t0008g0139a0001c0001t0027g0157a0001c0001t0033g0093others(6): Show | 9 | HG00280.hp1 HG01074.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+37052_249+3706 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(4): Show |
21 | a0001c0001t0006g0004a0001c0001t0009g0085a0001c0001t0015g0149others(18): Show | 21 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+37051_249+3706 others(15): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(5): Show |
14 | a0001c0001t0006g0003a0001c0001t0006g0198a0001c0001t0012g0131others(11): Show | 14 | HG01256.hp2 HG01496.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+37050_249+3706 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(6): Show |
11 | a0001c0001t0009g0104a0001c0001t0014g0112a0001c0001t0017g0105others(8): Show | 11 | HG00733.hp2 HG01167.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+37049_249+3706 others(17): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(7): Show |
5 | a0001c0001t0014g0142a0001c0001t0032g0121a0001c0001t0039g0106others(2): Show | 5 | HG01261.hp2 HG01361.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+37048_249+3706 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0063g0164a0001c0001t0133g0087 | 2 | HG02027.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.249+37047_249+3706 others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0009g0124a0001c0001t0015g0140a0001c0001t0050g0145others(1): Show | 4 | HG00621.hp2 HG00673.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+37046_249+3706 others(20): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0012g0111 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.249+37045_249+3706 others(21): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
A | ATTTTTTT others(11): Show |
2 | a0001c0001t0014g0159a0001c0001t0030g0147 | 2 | HG02738.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.249+37044_249+3706 others(22): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
AT | A | 8 | a0001c0001t0021g0170a0001c0001t0025g0173a0001c0001t0025g0174others(5): Show | 8 | HG01243.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+37061delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTT | A | 6 | a0001c0001t0008g0161a0001c0001t0018g0013a0001c0001t0062g0163others(3): Show | 6 | HG00735.hp2 HG01070.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+37057_249+3706 others(9): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0003g0009a0001c0001t0035g0229a0001c0001t0075g0137others(4): Show | 7 | HG00423.hp1 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+37054_249+3706 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0002g0073a0001c0001t0004g0076a0001c0001t0005g0053others(3): Show | 6 | HG02451.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+37053_249+3706 others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(3): Show |
A | 14 | a0001c0001t0008g0090a0001c0001t0013g0156a0001c0001t0017g0102others(11): Show | 14 | HG02074.hp2 HG02165.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+37052_249+3706 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0013g0153a0001c0001t0028g0231 | 2 | HG00673.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.249+37051_249+3706 others(15): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0016g0123a0001c0001t0031g0151 | 2 | HG02083.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+37050_249+3706 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(6): Show |
A | 15 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(12): Show | 15 | HG01496.hp1 HG02074.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.249+37049_249+3706 others(17): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(7): Show |
A | 41 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0046others(38): Show | 41 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.249+37048_249+3706 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(8): Show |
A | 3 | a0001c0001t0007g0017a0001c0001t0012g0130a0001c0001t0129g0196 | 3 | HG01074.hp2 HG03942.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.249+37047_249+3706 others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+37046_249+3706 others(20): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0049g0191 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.249+37043_249+3706 others(23): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(14): Show |
A | 4 | a0001c0001t0016g0119a0001c0001t0022g0109a0001c0001t0023g0108others(1): Show | 4 | HG00280.hp2 HG01516.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+37041_249+3706 others(25): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875589
|
ATTTTTTT others(17): Show |
A | 1 | a0001c0001t0003g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+37038_249+3706 others(28): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | |||||
chr12:65875965
|
G | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+37396G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875965 | ||||||
chr12:65876125
|
T | C | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+37556T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876125 | ||||||
chr12:65876226
|
CA | C | 59 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(56): Show | 59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.249+37667delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65876226 | |||||
chr12:65876329
|
G | C | 1 | a0001c0001t0130g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.249+37760G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876329 | ||||||
chr12:65876393
|
T | A | 1 | a0001c0001t0037g0141 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.249+37824T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876393 | ||||||
chr12:65876498
|
T | C | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+37929T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876498 | ||||||
chr12:65876610
|
A | G | 1 | a0001c0001t0035g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.249+38041A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876610 | ||||||
chr12:65876695
|
T | C | 1 | a0001c0001t0036g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.249+38126T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876695 | ||||||
chr12:65876904
|
G | A | 2 | a0001c0001t0056g0116a0002c0002t0020g0099 | 2 | HG02027.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.249+38335G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876904 | ||||||
chr12:65877208
|
G | A | 1 | a0001c0001t0111g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.249+38639G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877208 | ||||||
chr12:65877265
|
G | A | 1 | a0001c0001t0030g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.249+38696G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877265 | ||||||
chr12:65877439
|
G | C | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+38870G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877439 | ||||||
chr12:65877649
|
C | T | 1 | a0001c0001t0041g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.249+39080C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877649 | ||||||
chr12:65877814
|
C | CA | 18 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(15): Show | 18 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.249+39255dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65877814 | |||||
chr12:65877860
|
A | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0111g0227others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+39291A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877860 | ||||||
chr12:65877896
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.249+39327G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877896 | ||||||
chr12:65877901
|
C | T | 1 | a0001c0001t0029g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.249+39332C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877901 | ||||||
chr12:65878422
|
G | A | 29 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(26): Show | 29 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.249+39853G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878422 | ||||||
chr12:65878579
|
G | T | 5 | a0001c0001t0004g0058a0001c0001t0004g0074a0001c0001t0005g0059others(2): Show | 5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+40010G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878579 | ||||||
chr12:65878952
|
A | G | 18 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(15): Show | 18 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.249+40383A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878952 | ||||||
chr12:65878990
|
T | C | 1 | a0001c0001t0085g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.249+40421T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878990 | ||||||
chr12:65879000
|
T | C | 1 | a0001c0001t0063g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.249+40431T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879000 | ||||||
chr12:65879291
|
T | TA | 80 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(77): Show | 80 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.249+40723dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65879291 | |||||
chr12:65879292
|
A | AAT | 31 | a0001c0001t0001g0045a0001c0001t0003g0190a0001c0001t0003g0208others(28): Show | 31 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.249+40723_249+4072 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879292 | ||||||
chr12:65879292
|
AT | A | 11 | a0001c0001t0039g0106a0001c0001t0046g0169a0001c0001t0047g0183others(8): Show | 11 | HG01361.hp1 HG02683.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+40739delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65879292 | |||||
chr12:65879294
|
T | A | 8 | a0001c0001t0046g0169a0001c0001t0047g0183a0001c0001t0047g0185others(5): Show | 8 | HG02683.hp1 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+40725T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879294 | ||||||
chr12:65879483
|
T | G | 2 | a0001c0001t0104g0216a0001c0001t0109g0012 | 2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.249+40914T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879483 | ||||||
chr12:65879719
|
G | A | 2 | a0001c0001t0006g0204a0001c0001t0049g0191 | 2 | NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.249+41150G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879719 | ||||||
chr12:65879833
|
T | A | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+41264T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879833 | ||||||
chr12:65879871
|
A | G | 3 | a0001c0001t0004g0058a0001c0001t0005g0059a0001c0001t0010g0057 | 3 | HG02040.hp1 HG02135.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.249+41302A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879871 | ||||||
chr12:65880789
|
A | G | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+42220A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65880789 | ||||||
chr12:65880815
|
A | T | 3 | a0001c0001t0007g0017a0001c0001t0043g0018a0001c0001t0103g0019 | 3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.249+42246A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65880815 | ||||||
chr12:65880931
|
C | T | 4 | a0001c0001t0018g0223a0001c0001t0018g0225a0001c0001t0098g0030others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+42362C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65880931 | ||||||
chr12:65881052
|
T | C | 1 | a0001c0001t0054g0177 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+42483T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881052 | ||||||
chr12:65881271
|
T | A | 1 | a0001c0001t0035g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.249+42702T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881271 | ||||||
chr12:65881293
|
TC | T | 2 | a0001c0001t0048g0199a0001c0001t0048g0215 | 2 | NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.249+42725delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881293 | ||||||
chr12:65881455
|
T | TA | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+42894dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65881455 | |||||
chr12:65881979
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.249+43410C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881979 | ||||||
chr12:65882303
|
G | C | 1 | a0001c0001t0063g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.249+43734G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882303 | ||||||
chr12:65882419
|
C | T | 18 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(15): Show | 18 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.249+43850C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882419 | ||||||
chr12:65882662
|
G | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+44093G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882662 | ||||||
chr12:65882902
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.249+44333G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882902 | ||||||
chr12:65882973
|
G | A | 1 | a0001c0001t0018g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+44404G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882973 | ||||||
chr12:65883194
|
C | T | 2 | a0001c0001t0011g0066a0001c0001t0011g0067 | 2 | NA18970.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.249+44625C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883194 | ||||||
chr12:65883233
|
T | C | 1 | a0001c0001t0023g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.249+44664T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883233 | ||||||
chr12:65883283
|
G | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+44714G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883283 | ||||||
chr12:65883420
|
A | C | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+44851A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883420 | ||||||
chr12:65883529
|
C | T | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+44960C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883529 | ||||||
chr12:65883869
|
C | T | 1 | a0001c0001t0023g0132 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.249+45300C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883869 | ||||||
chr12:65883918
|
A | T | 113 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(110): Show | 113 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.249+45349A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883918 | ||||||
chr12:65884011
|
G | A | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+45442G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884011 | ||||||
chr12:65884083
|
C | A | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+45514C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884083 | ||||||
chr12:65884132
|
C | G | 1 | a0001c0001t0098g0030 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.249+45563C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884132 | ||||||
chr12:65884218
|
T | C | 5 | a0001c0001t0004g0058a0001c0001t0004g0074a0001c0001t0005g0059others(2): Show | 5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+45649T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884218 | ||||||
chr12:65884952
|
C | T | 1 | a0001c0001t0030g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.249+46383C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884952 | ||||||
chr12:65885141
|
A | G | 1 | a0001c0001t0117g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.249+46572A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885141 | ||||||
chr12:65885193
|
G | A | 1 | a0001c0001t0036g0098 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.249+46624G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885193 | ||||||
chr12:65885313
|
G | A | 2 | a0001c0001t0022g0109a0001c0001t0023g0108 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.249+46744G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885313 | ||||||
chr12:65885319
|
T | A | 44 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(41): Show | 44 | HG00558.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.249+46750T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885319 | ||||||
chr12:65885382
|
A | C | 1 | a0001c0001t0010g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.249+46813A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885382 | ||||||
chr12:65885489
|
C | A | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+46920C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885489 | ||||||
chr12:65885520
|
A | G | 1 | a0001c0001t0031g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.249+46951A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885520 | ||||||
chr12:65885816
|
T | C | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+47247T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885816 | ||||||
chr12:65885838
|
G | A | 26 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+47269G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885838 | ||||||
chr12:65885931
|
T | G | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+47362T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885931 | ||||||
chr12:65886042
|
C | A | 24 | a0001c0001t0003g0208a0001c0001t0003g0213a0001c0001t0003g0214others(21): Show | 24 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.249+47473C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886042 | ||||||
chr12:65886095
|
A | G | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+47526A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886095 | ||||||
chr12:65886363
|
C | CT | 7 | a0001c0001t0003g0208a0001c0001t0019g0207a0001c0001t0019g0209others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+47808dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65886363 | |||||
chr12:65886364
|
T | TC | 41 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(38): Show | 41 | HG00558.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.249+47795_249+4779 others(5): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886364 | ||||||
chr12:65886365
|
T | C | 3 | a0001c0001t0001g0041a0001c0001t0104g0216a0001c0001t0109g0012 | 3 | HG03041.hp1 HG03209.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.249+47796T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886365 | ||||||
chr12:65886463
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+47894G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886463 | ||||||
chr12:65886471
|
T | C | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+47902T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886471 | ||||||
chr12:65886705
|
C | A | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+48136C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886705 | ||||||
chr12:65886734
|
C | T | 1 | a0001c0001t0125g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.249+48165C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886734 | ||||||
chr12:65886804
|
C | G | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.249+48235C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886804 | ||||||
chr12:65886965
|
C | T | 1 | a0001c0001t0087g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.249+48396C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886965 | ||||||
chr12:65886967
|
G | A | 1 | a0001c0001t0033g0093 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.249+48398G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886967 | ||||||
chr12:65887143
|
A | G | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+48574A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887143 | ||||||
chr12:65887173
|
A | G | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+48604A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887173 | ||||||
chr12:65887394
|
C | A | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+48825C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887394 | ||||||
chr12:65887568
|
C | A | 26 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+48999C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887568 | ||||||
chr12:65887815
|
C | T | 1 | a0001c0001t0007g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.249+49246C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887815 | ||||||
chr12:65887828
|
T | C | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+49259T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887828 | ||||||
chr12:65887877
|
TA | T | 113 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(110): Show | 113 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.249+49322delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65887877 | |||||
chr12:65887878
|
A | T | 1 | a0001c0001t0024g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.249+49309A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887878 | ||||||
chr12:65888100
|
C | T | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+49531C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888100 | ||||||
chr12:65888228
|
G | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+49659G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888228 | ||||||
chr12:65888479
|
A | G | 1 | a0001c0001t0005g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.249+49910A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888479 | ||||||
chr12:65888512
|
A | G | 1 | a0001c0001t0004g0025 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.249+49943A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888512 | ||||||
chr12:65888551
|
GCT | G | 3 | a0001c0001t0034g0094a0001c0001t0035g0148a0001c0001t0094g0235 | 3 | HG01516.hp2 HG03017.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.249+49985_249+4998 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888551 | |||||
chr12:65888554
|
C | CT | 61 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0033others(58): Show | 61 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.249+50012dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | |||||
chr12:65888554
|
C | CTT | 50 | a0001c0001t0001g0032a0001c0001t0001g0054a0001c0001t0002g0070others(47): Show | 50 | HG00423.hp2 HG00621.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.249+50011_249+5001 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | |||||
chr12:65888554
|
C | CTTT | 21 | a0001c0001t0001g0045a0001c0001t0002g0060a0001c0001t0002g0061others(18): Show | 21 | HG00609.hp2 HG01074.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+50010_249+5001 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | |||||
chr12:65888554
|
CT | C | 52 | a0001c0001t0005g0015a0001c0001t0006g0003a0001c0001t0006g0197others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.249+50012delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | |||||
chr12:65888554
|
CTT | C | 15 | a0001c0001t0006g0004a0001c0001t0009g0104a0001c0001t0017g0102others(12): Show | 15 | HG01258.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.249+50011_249+5001 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | |||||
chr12:65888595
|
ACT | A | 38 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(35): Show | 38 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.249+50029_249+5003 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888595 | |||||
chr12:65888664
|
T | C | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+50095T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888664 | ||||||
chr12:65888688
|
T | C | 1 | a0001c0001t0119g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.249+50119T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888688 | ||||||
chr12:65888721
|
G | C | 9 | a0001c0001t0006g0198a0001c0001t0009g0104a0001c0001t0017g0102others(6): Show | 9 | HG01258.hp1 HG01361.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+50152G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888721 | ||||||
chr12:65888725
|
G | T | 27 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(24): Show | 27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+50156G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888725 | ||||||
chr12:65888731
|
C | T | 1 | a0001c0001t0120g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.249+50162C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888731 | ||||||
chr12:65888772
|
C | T | 1 | a0001c0001t0011g0027 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.249+50203C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888772 | ||||||
chr12:65888814
|
C | T | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+50245C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888814 | ||||||
chr12:65888852
|
G | C | 103 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(100): Show | 103 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.249+50283G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888852 | ||||||
chr12:65888864
|
C | T | 37 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(34): Show | 37 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.249+50295C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888864 | ||||||
chr12:65889031
|
G | C | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+50462G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889031 | ||||||
chr12:65889139
|
C | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+50570C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889139 | ||||||
chr12:65889378
|
A | G | 1 | a0001c0001t0036g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.249+50809A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889378 | ||||||
chr12:65889444
|
A | G | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+50875A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889444 | ||||||
chr12:65889453
|
T | A | 27 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(24): Show | 27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+50884T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889453 | ||||||
chr12:65889455
|
C | T | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+50886C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889455 | ||||||
chr12:65889742
|
A | G | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249+51173A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889742 | ||||||
chr12:65889794
|
G | A | 12 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(9): Show | 12 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+51225G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889794 | ||||||
chr12:65889820
|
T | C | 27 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(24): Show | 27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+51251T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889820 | ||||||
chr12:65889865
|
T | A | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+51296T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889865 | ||||||
chr12:65889893
|
T | C | 19 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(16): Show | 19 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+51324T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889893 | ||||||
chr12:65890019
|
T | C | 1 | a0001c0001t0045g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.249+51450T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890019 | ||||||
chr12:65890556
|
C | T | 76 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0006g0197others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.249+51987C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890556 | ||||||
chr12:65890655
|
T | C | 1 | a0001c0001t0125g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.249+52086T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890655 | ||||||
chr12:65890710
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.249+52141C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890710 | ||||||
chr12:65890727
|
C | CT | 10 | a0001c0001t0004g0038a0001c0001t0006g0003a0001c0001t0006g0004others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.249+52173dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65890727 | |||||
chr12:65890727
|
CT | C | 39 | a0001c0001t0002g0073a0001c0001t0003g0190a0001c0001t0003g0208others(36): Show | 39 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.249+52173delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65890727 | |||||
chr12:65890765
|
C | T | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+52196C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890765 | ||||||
chr12:65891051
|
A | G | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+52482A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891051 | ||||||
chr12:65891065
|
C | A | 2 | a0001c0001t0037g0141a0001c0001t0087g0086 | 2 | HG02300.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.249+52496C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891065 | ||||||
chr12:65891093
|
T | C | 112 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(109): Show | 112 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.249+52524T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891093 | ||||||
chr12:65891405
|
CAAT | C | 2 | a0001c0001t0048g0199a0001c0001t0048g0215 | 2 | NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.249+52841_249+5284 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65891405 | |||||
chr12:65891479
|
G | A | 1 | a0001c0001t0030g0136 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.249+52910G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891479 | ||||||
chr12:65891578
|
C | T | 1 | a0001c0001t0132g0028 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.249+53009C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891578 | ||||||
chr12:65891605
|
G | A | 1 | a0001c0001t0122g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.249+53036G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891605 | ||||||
chr12:65891788
|
G | T | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+53219G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891788 | ||||||
chr12:65892354
|
C | T | 1 | a0001c0001t0008g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+53785C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892354 | ||||||
chr12:65892742
|
G | A | 3 | a0001c0001t0007g0017a0001c0001t0043g0018a0001c0001t0103g0019 | 3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.249+54173G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892742 | ||||||
chr12:65892785
|
C | T | 1 | a0001c0001t0102g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.249+54216C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892785 | ||||||
chr12:65892815
|
T | A | 1 | a0001c0001t0035g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.249+54246T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892815 | ||||||
chr12:65892831
|
A | G | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+54262A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892831 | ||||||
chr12:65892957
|
G | A | 3 | a0001c0001t0006g0197a0001c0001t0040g0091a0001c0001t0071g0092 | 3 | NA18951.hp2 NA18957.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.249+54388G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892957 | ||||||
chr12:65893005
|
G | A | 1 | a0001c0001t0014g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.249+54436G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893005 | ||||||
chr12:65893035
|
G | A | 1 | a0001c0001t0107g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.249+54466G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893035 | ||||||
chr12:65893106
|
C | A | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+54537C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893106 | ||||||
chr12:65893160
|
A | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+54591A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893160 | ||||||
chr12:65893539
|
A | G | 1 | a0001c0001t0072g0162 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.249+54970A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893539 | ||||||
chr12:65894000
|
G | A | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+55431G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894000 | ||||||
chr12:65894194
|
C | G | 3 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0060g0172 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+55625C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894194 | ||||||
chr12:65894484
|
T | A | 1 | a0001c0001t0009g0124 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.249+55915T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894484 | ||||||
chr12:65894748
|
A | G | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+56179A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894748 | ||||||
chr12:65894854
|
T | C | 1 | a0001c0001t0130g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.249+56285T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894854 | ||||||
chr12:65894999
|
G | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-56384G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894999 | ||||||
chr12:65895344
|
A | G | 1 | a0001c0001t0038g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250-56039A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895344 | ||||||
chr12:65895441
|
C | T | 9 | a0001c0001t0021g0170a0001c0001t0021g0171a0001c0001t0025g0173others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-55942C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895441 | ||||||
chr12:65895844
|
T | G | 2 | a0001c0001t0098g0030a0001c0001t0112g0224 | 2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.250-55539T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895844 | ||||||
chr12:65895953
|
A | C | 40 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(37): Show | 40 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.250-55430A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895953 | ||||||
chr12:65896072
|
G | A | 1 | a0001c0001t0014g0112 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.250-55311G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896072 | ||||||
chr12:65896597
|
C | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-54786C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896597 | ||||||
chr12:65896768
|
C | T | 3 | a0001c0001t0003g0213a0001c0001t0003g0214a0001c0001t0014g0142 | 3 | HG01256.hp1 HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.250-54615C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896768 | ||||||
chr12:65896786
|
T | G | 1 | a0001c0001t0028g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.250-54597T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896786 | ||||||
chr12:65897147
|
T | C | 3 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0042g0047 | 3 | HG02818.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.250-54236T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897147 | ||||||
chr12:65897452
|
T | C | 39 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 39 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.250-53931T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897452 | ||||||
chr12:65897462
|
G | A | 3 | a0001c0001t0006g0197a0001c0001t0040g0091a0001c0001t0071g0092 | 3 | NA18951.hp2 NA18957.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.250-53921G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897462 | ||||||
chr12:65897594
|
C | T | 27 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(24): Show | 27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.250-53789C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897594 | ||||||
chr12:65897620
|
G | A | 1 | a0001c0001t0110g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.250-53763G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897620 | ||||||
chr12:65897652
|
A | C | 20 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(17): Show | 20 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-53731A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897652 | ||||||
chr12:65897681
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.250-53702C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897681 | ||||||
chr12:65897685
|
C | T | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-53698C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897685 | ||||||
chr12:65897831
|
G | T | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-53552G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897831 | ||||||
chr12:65897941
|
A | G | 98 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(95): Show | 98 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.250-53442A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897941 | ||||||
chr12:65897964
|
C | CA | 42 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(39): Show | 42 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.250-53403dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65897964 | |||||
chr12:65897964
|
CA | C | 22 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(19): Show | 22 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.250-53403delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65897964 | |||||
chr12:65898005
|
G | T | 7 | a0001c0001t0006g0197a0001c0001t0006g0228a0001c0001t0013g0153others(4): Show | 7 | HG00673.hp1 HG02155.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-53378G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898005 | ||||||
chr12:65898202
|
A | G | 9 | a0001c0001t0009g0001a0001c0001t0017g0194a0001c0001t0037g0201others(6): Show | 9 | HG00609.hp2 HG00621.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-53181A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898202 | ||||||
chr12:65898208
|
T | A | 1 | a0001c0001t0131g0222 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-53175T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898208 | ||||||
chr12:65898451
|
G | A | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-52932G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898451 | ||||||
chr12:65898644
|
G | A | 7 | a0001c0001t0004g0038a0001c0001t0015g0149a0001c0001t0016g0119others(4): Show | 7 | HG00140.hp1 HG00280.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-52739G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898644 | ||||||
chr12:65898656
|
T | G | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-52727T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898656 | ||||||
chr12:65898771
|
G | A | 4 | a0001c0001t0018g0223a0001c0001t0018g0225a0001c0001t0098g0030others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-52612G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898771 | ||||||
chr12:65898841
|
G | C | 1 | a0001c0001t0002g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.250-52542G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898841 | ||||||
chr12:65898904
|
C | T | 1 | a0001c0001t0114g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.250-52479C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898904 | ||||||
chr12:65898913
|
G | A | 1 | a0001c0001t0127g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.250-52470G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898913 | ||||||
chr12:65898936
|
C | T | 1 | a0001c0001t0078g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-52447C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898936 | ||||||
chr12:65898991
|
C | T | 7 | a0001c0001t0008g0090a0001c0001t0008g0161a0001c0001t0029g0082others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-52392C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898991 | ||||||
chr12:65899043
|
C | CA | 31 | a0001c0001t0002g0073a0001c0001t0004g0076a0001c0001t0005g0053others(28): Show | 31 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.250-52311dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | |||||
chr12:65899043
|
C | CAA | 11 | a0001c0001t0003g0187a0001c0001t0008g0139a0001c0001t0009g0085others(8): Show | 11 | HG00741.hp2 HG01258.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-52312_250-5231 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | |||||
chr12:65899043
|
CA | C | 23 | a0001c0001t0001g0029a0001c0001t0002g0061a0001c0001t0007g0022others(20): Show | 23 | HG00280.hp2 HG00733.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.250-52311delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | |||||
chr12:65899043
|
CAA | C | 59 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(56): Show | 59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.250-52312_250-5231 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | |||||
chr12:65899043
|
CAAA | C | 7 | a0001c0001t0007g0017a0001c0001t0007g0021a0001c0001t0016g0123others(4): Show | 7 | HG00741.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-52313_250-5231 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | |||||
chr12:65899097
|
G | A | 1 | a0001c0001t0117g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.250-52286G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899097 | ||||||
chr12:65899291
|
T | C | 8 | a0001c0001t0009g0001a0001c0001t0017g0194a0001c0001t0038g0193others(5): Show | 8 | HG00609.hp2 HG00621.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-52092T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899291 | ||||||
chr12:65899918
|
A | G | 1 | a0001c0001t0019g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.250-51465A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899918 | ||||||
chr12:65899993
|
T | G | 4 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0065others(1): Show | 4 | HG00558.hp2 HG02132.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-51390T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899993 | ||||||
chr12:65900015
|
C | G | 103 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(100): Show | 103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-51368C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900015 | ||||||
chr12:65900096
|
T | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-51287T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900096 | ||||||
chr12:65900814
|
G | A | 4 | a0001c0001t0037g0141a0001c0001t0039g0127a0001c0001t0087g0086others(1): Show | 4 | HG00735.hp1 HG02300.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-50569G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900814 | ||||||
chr12:65900854
|
G | T | 5 | a0001c0001t0004g0058a0001c0001t0004g0074a0001c0001t0005g0059others(2): Show | 5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-50529G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900854 | ||||||
chr12:65901010
|
G | A | 1 | a0001c0001t0044g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250-50373G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901010 | ||||||
chr12:65901072
|
G | C | 1 | a0001c0001t0010g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250-50311G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901072 | ||||||
chr12:65901232
|
A | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-50151A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901232 | ||||||
chr12:65901316
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.250-50067C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901316 | ||||||
chr12:65901323
|
A | G | 112 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(109): Show | 112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.250-50060A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901323 | ||||||
chr12:65901493
|
C | T | 7 | a0001c0001t0004g0025a0001c0001t0005g0064a0001c0001t0007g0063others(4): Show | 7 | HG02083.hp2 NA18942.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-49890C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901493 | ||||||
chr12:65901790
|
T | C | 112 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(109): Show | 112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.250-49593T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901790 | ||||||
chr12:65901906
|
A | C | 1 | a0001c0001t0013g0107 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250-49477A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901906 | ||||||
chr12:65901992
|
A | G | 1 | a0001c0001t0044g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250-49391A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901992 | ||||||
chr12:65902010
|
C | G | 1 | a0001c0001t0108g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250-49373C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902010 | ||||||
chr12:65902026
|
T | G | 1 | a0001c0001t0108g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250-49357T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902026 | ||||||
chr12:65902056
|
A | G | 1 | a0001c0001t0091g0129 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.250-49327A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902056 | ||||||
chr12:65902067
|
T | G | 4 | a0001c0001t0018g0223a0001c0001t0018g0225a0001c0001t0098g0030others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-49316T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902067 | ||||||
chr12:65902166
|
GT | G | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-49207delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65902166 | |||||
chr12:65902167
|
T | G | 1 | a0001c0001t0032g0121 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.250-49216T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902167 | ||||||
chr12:65902218
|
A | G | 1 | a0001c0001t0125g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.250-49165A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902218 | ||||||
chr12:65902295
|
C | T | 1 | a0001c0001t0009g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-49088C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902295 | ||||||
chr12:65902540
|
T | C | 2 | a0001c0001t0016g0113a0001c0001t0096g0234 | 2 | HG00280.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.250-48843T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902540 | ||||||
chr12:65902958
|
T | A | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-48425T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902958 | ||||||
chr12:65902973
|
G | A | 1 | a0001c0001t0074g0150 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.250-48410G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902973 | ||||||
chr12:65903045
|
G | T | 20 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(17): Show | 20 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-48338G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65903045 | ||||||
chr12:65903316
|
T | C | 1 | a0001c0001t0003g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.250-48067T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65903316 | ||||||
chr12:65903499
|
T | C | 39 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 39 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.250-47884T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65903499 | ||||||
chr12:65903629
|
A | AT | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-47745dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65903629 | |||||
chr12:65904031
|
C | T | 103 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(100): Show | 103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-47352C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904031 | ||||||
chr12:65904175
|
TCATAGAA others(20): Show |
T | 1 | a0001c0001t0018g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-47206_250-4718 others(31): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65904175 | |||||
chr12:65904251
|
C | T | 101 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 101 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.250-47132C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904251 | ||||||
chr12:65904254
|
G | A | 8 | a0001c0001t0003g0208a0001c0001t0003g0213a0001c0001t0003g0214others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-47129G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904254 | ||||||
chr12:65904306
|
C | T | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-47077C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904306 | ||||||
chr12:65904368
|
A | G | 3 | a0001c0001t0054g0177a0001c0001t0057g0233a0001c0001t0102g0218 | 3 | HG02257.hp2 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.250-47015A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904368 | ||||||
chr12:65904388
|
A | G | 1 | a0001c0001t0075g0137 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.250-46995A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904388 | ||||||
chr12:65904399
|
C | T | 112 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(109): Show | 112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.250-46984C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904399 | ||||||
chr12:65904762
|
A | G | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-46621A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904762 | ||||||
chr12:65904908
|
G | A | 6 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-46475G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904908 | ||||||
chr12:65904922
|
A | G | 37 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(34): Show | 37 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.250-46461A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904922 | ||||||
chr12:65904996
|
C | T | 1 | a0001c0001t0036g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.250-46387C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904996 | ||||||
chr12:65904998
|
C | T | 1 | a0001c0001t0018g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.250-46385C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904998 | ||||||
chr12:65905182
|
T | TCA | 8 | a0001c0001t0010g0031a0001c0001t0042g0071a0001c0001t0047g0183others(5): Show | 8 | HG01192.hp2 HG02258.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-46178_250-4617 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65905182 | |||||
chr12:65905182
|
T | TCACA | 38 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(35): Show | 38 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.250-46180_250-4617 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65905182 | |||||
chr12:65905182
|
T | TCACACA | 9 | a0001c0001t0018g0223a0001c0001t0025g0173a0001c0001t0025g0174others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-46182_250-4617 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65905182 | |||||
chr12:65905269
|
T | G | 1 | a0001c0001t0031g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.250-46114T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905269 | ||||||
chr12:65905362
|
C | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-46021C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905362 | ||||||
chr12:65905966
|
AGTCATTA others(8): Show |
A | 103 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(100): Show | 103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-45416_250-4540 others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905966 | ||||||
chr12:65905983
|
C | A | 103 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(100): Show | 103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-45400C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905983 | ||||||
chr12:65906255
|
A | G | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-45128A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65906255 | ||||||
chr12:65906539
|
C | A | 37 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(34): Show | 37 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.250-44844C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65906539 | ||||||
chr12:65906603
|
G | A | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-44780G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65906603 | ||||||
chr12:65907052
|
T | A | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-44331T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907052 | ||||||
chr12:65907163
|
G | A | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-44220G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907163 | ||||||
chr12:65907202
|
C | T | 1 | a0001c0001t0036g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.250-44181C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907202 | ||||||
chr12:65907411
|
C | CA | 39 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0214others(36): Show | 39 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.250-43952dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65907411 | |||||
chr12:65907411
|
CA | C | 10 | a0001c0001t0004g0058a0001c0001t0005g0059a0001c0001t0007g0063others(7): Show | 10 | HG00741.hp1 HG01361.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-43952delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65907411 | |||||
chr12:65907435
|
G | A | 1 | a0001c0001t0015g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.250-43948G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907435 | ||||||
chr12:65907436
|
G | T | 1 | a0001c0001t0015g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.250-43947G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907436 | ||||||
chr12:65907638
|
C | T | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-43745C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907638 | ||||||
chr12:65907769
|
C | T | 1 | a0001c0001t0051g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.250-43614C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907769 | ||||||
chr12:65907831
|
A | G | 1 | a0001c0001t0008g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.250-43552A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907831 | ||||||
chr12:65907969
|
T | A | 1 | a0001c0001t0074g0150 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.250-43414T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907969 | ||||||
chr12:65908226
|
C | T | 1 | a0001c0001t0128g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.250-43157C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908226 | ||||||
chr12:65908230
|
C | T | 8 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-43153C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908230 | ||||||
chr12:65908509
|
C | T | 1 | a0001c0001t0070g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.250-42874C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908509 | ||||||
chr12:65908821
|
A | G | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-42562A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908821 | ||||||
chr12:65909085
|
G | T | 19 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(16): Show | 19 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-42298G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909085 | ||||||
chr12:65909288
|
T | G | 1 | a0001c0001t0122g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.250-42095T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909288 | ||||||
chr12:65909396
|
T | A | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-41987T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909396 | ||||||
chr12:65909456
|
T | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-41927T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909456 | ||||||
chr12:65909472
|
T | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-41911T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909472 | ||||||
chr12:65909719
|
T | C | 1 | a0001c0001t0123g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.250-41664T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909719 | ||||||
chr12:65909754
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.250-41629G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909754 | ||||||
chr12:65909900
|
C | T | 1 | a0001c0001t0028g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.250-41483C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909900 | ||||||
chr12:65909955
|
G | A | 102 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(99): Show | 102 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.250-41428G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909955 | ||||||
chr12:65910056
|
G | A | 5 | a0001c0001t0004g0058a0001c0001t0004g0074a0001c0001t0005g0059others(2): Show | 5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-41327G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910056 | ||||||
chr12:65910060
|
G | A | 1 | a0001c0001t0099g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-41323G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910060 | ||||||
chr12:65910070
|
G | C | 1 | a0001c0001t0099g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-41313G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910070 | ||||||
chr12:65910546
|
A | G | 1 | a0001c0001t0019g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.250-40837A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910546 | ||||||
chr12:65910618
|
G | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-40765G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910618 | ||||||
chr12:65910793
|
T | C | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-40590T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910793 | ||||||
chr12:65910864
|
G | A | 7 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0035g0229others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-40519G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910864 | ||||||
chr12:65910972
|
C | G | 9 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0018g0223others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-40411C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910972 | ||||||
chr12:65911454
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.250-39929C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911454 | ||||||
chr12:65911514
|
G | A | 19 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(16): Show | 19 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-39869G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911514 | ||||||
chr12:65911615
|
A | T | 1 | a0001c0001t0005g0059 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.250-39768A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911615 | ||||||
chr12:65911923
|
C | T | 11 | a0001c0001t0009g0001a0001c0001t0017g0194a0001c0001t0037g0201others(8): Show | 11 | HG00609.hp2 HG00621.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-39460C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911923 | ||||||
chr12:65912583
|
T | C | 1 | a0001c0001t0102g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.250-38800T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65912583 | ||||||
chr12:65912602
|
G | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-38781G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65912602 | ||||||
chr12:65912661
|
A | C | 197 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.250-38722A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65912661 | ||||||
chr12:65913089
|
T | C | 19 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(16): Show | 19 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-38294T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913089 | ||||||
chr12:65913090
|
T | G | 3 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0065 | 3 | HG02132.hp1 NA18959.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.250-38293T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913090 | ||||||
chr12:65913311
|
C | T | 1 | a0001c0001t0103g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.250-38072C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913311 | ||||||
chr12:65913321
|
C | T | 1 | a0001c0001t0060g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250-38062C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913321 | ||||||
chr12:65913353
|
G | A | 7 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0035g0229others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-38030G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913353 | ||||||
chr12:65913438
|
G | A | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-37945G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913438 | ||||||
chr12:65913567
|
G | A | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.250-37816G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913567 | ||||||
chr12:65913860
|
C | T | 1 | a0001c0001t0024g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.250-37523C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913860 | ||||||
chr12:65913900
|
A | G | 1 | a0001c0001t0015g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.250-37483A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913900 | ||||||
chr12:65914050
|
A | G | 114 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(111): Show | 114 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.250-37333A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914050 | ||||||
chr12:65914168
|
A | T | 2 | a0001c0001t0006g0204a0001c0001t0049g0191 | 2 | NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.250-37215A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914168 | ||||||
chr12:65914421
|
C | T | 1 | a0001c0001t0127g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.250-36962C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914421 | ||||||
chr12:65914448
|
T | A | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-36935T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914448 | ||||||
chr12:65914522
|
T | C | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-36861T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914522 | ||||||
chr12:65914545
|
A | T | 1 | a0001c0001t0067g0138 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250-36838A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914545 | ||||||
chr12:65914645
|
A | T | 3 | a0001c0001t0016g0123a0001c0001t0028g0231a0001c0001t0111g0227 | 3 | HG00741.hp1 HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-36738A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914645 | ||||||
chr12:65914668
|
G | T | 1 | a0001c0001t0084g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.250-36715G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914668 | ||||||
chr12:65914696
|
C | T | 1 | a0001c0001t0030g0147 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.250-36687C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914696 | ||||||
chr12:65914745
|
G | A | 1 | a0001c0001t0099g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-36638G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914745 | ||||||
chr12:65914864
|
A | G | 114 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(111): Show | 114 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.250-36519A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914864 | ||||||
chr12:65914919
|
C | T | 1 | a0001c0001t0046g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.250-36464C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914919 | ||||||
chr12:65915008
|
C | A | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-36375C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915008 | ||||||
chr12:65915079
|
C | G | 1 | a0001c0001t0096g0234 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.250-36304C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915079 | ||||||
chr12:65915135
|
T | C | 2 | a0001c0001t0020g0100a0001c0001t0050g0145 | 2 | HG00673.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.250-36248T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915135 | ||||||
chr12:65915416
|
G | GT | 20 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(17): Show | 20 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-35966dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65915416 | |||||
chr12:65915424
|
T | C | 1 | a0001c0001t0010g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250-35959T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915424 | ||||||
chr12:65915818
|
A | G | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-35565A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915818 | ||||||
chr12:65915946
|
G | C | 1 | a0001c0001t0131g0222 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-35437G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915946 | ||||||
chr12:65916146
|
A | G | 1 | a0002c0002t0020g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250-35237A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916146 | ||||||
chr12:65916217
|
C | G | 26 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-35166C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916217 | ||||||
chr12:65916218
|
C | T | 26 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0003g0213others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-35165C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916218 | ||||||
chr12:65916292
|
G | A | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-35091G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916292 | ||||||
chr12:65916766
|
A | G | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-34617A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916766 | ||||||
chr12:65916815
|
G | T | 1 | a0001c0001t0119g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.250-34568G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916815 | ||||||
chr12:65916888
|
T | G | 1 | a0001c0001t0046g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.250-34495T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916888 | ||||||
chr12:65917277
|
C | T | 1 | a0001c0001t0025g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.250-34106C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917277 | ||||||
chr12:65917465
|
C | G | 1 | a0001c0001t0042g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.250-33918C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917465 | ||||||
chr12:65917730
|
G | C | 1 | a0001c0001t0008g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.250-33653G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917730 | ||||||
chr12:65917749
|
G | A | 1 | a0001c0001t0011g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.250-33634G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917749 | ||||||
chr12:65918240
|
T | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-33143T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918240 | ||||||
chr12:65918476
|
T | G | 8 | a0001c0001t0006g0004a0001c0001t0018g0223a0001c0001t0098g0030others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-32907T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918476 | ||||||
chr12:65918658
|
G | A | 8 | a0001c0001t0006g0004a0001c0001t0018g0223a0001c0001t0098g0030others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-32725G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918658 | ||||||
chr12:65918665
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.250-32718G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918665 | ||||||
chr12:65918704
|
G | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-32679G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918704 | ||||||
chr12:65918978
|
G | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-32405G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918978 | ||||||
chr12:65919422
|
T | G | 2 | a0001c0001t0027g0157a0001c0001t0031g0151 | 2 | HG02083.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.250-31961T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65919422 | ||||||
chr12:65919730
|
G | A | 1 | a0001c0001t0125g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.250-31653G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65919730 | ||||||
chr12:65920186
|
G | A | 1 | a0001c0001t0074g0150 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.250-31197G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920186 | ||||||
chr12:65920568
|
A | G | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-30815A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920568 | ||||||
chr12:65920640
|
C | T | 2 | a0001c0001t0044g0051a0001c0001t0044g0052 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.250-30743C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920640 | ||||||
chr12:65920685
|
C | T | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-30698C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920685 | ||||||
chr12:65920804
|
C | T | 3 | a0001c0001t0018g0223a0001c0001t0098g0030a0001c0001t0112g0224 | 3 | HG02559.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.250-30579C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920804 | ||||||
chr12:65920879
|
T | A | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-30504T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920879 | ||||||
chr12:65920881
|
G | A | 21 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(18): Show | 21 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-30502G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920881 | ||||||
chr12:65920886
|
G | A | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0108g0180others(2): Show | 5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-30497G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920886 | ||||||
chr12:65920979
|
A | T | 19 | a0001c0001t0003g0213a0001c0001t0003g0214a0001c0001t0008g0080others(16): Show | 19 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.250-30404A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920979 | ||||||
chr12:65921018
|
T | C | 3 | a0001c0001t0046g0169a0001c0001t0105g0168a0001c0001t0106g0167 | 3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.250-30365T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921018 | ||||||
chr12:65921040
|
G | T | 1 | a0001c0001t0018g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.250-30343G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921040 | ||||||
chr12:65921127
|
T | C | 2 | a0001c0001t0016g0123a0001c0001t0028g0231 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-30256T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921127 | ||||||
chr12:65921164
|
T | C | 3 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008 | 3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.250-30219T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921164 | ||||||
chr12:65921507
|
A | G | 9 | a0001c0001t0018g0013a0001c0001t0025g0173a0001c0001t0025g0174others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-29876A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921507 | ||||||
chr12:65921599
|
CCTGA | C | 21 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(18): Show | 21 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-29781_250-2977 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65921599 | |||||
chr12:65921699
|
C | G | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-29684C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921699 | ||||||
chr12:65921996
|
A | G | 1 | a0001c0001t0079g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.250-29387A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921996 | ||||||
chr12:65922118
|
T | C | 101 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0033others(98): Show | 101 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.250-29265T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922118 | ||||||
chr12:65922218
|
C | T | 10 | a0001c0001t0003g0190a0001c0001t0003g0208a0001c0001t0019g0207others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-29165C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922218 | ||||||
chr12:65922263
|
C | G | 3 | a0001c0001t0002g0073a0001c0001t0004g0076a0001c0001t0005g0053 | 3 | HG02451.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-29120C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922263 | ||||||
chr12:65922309
|
G | A | 1 | a0001c0001t0102g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.250-29074G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922309 | ||||||
chr12:65922601
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.250-28782G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922601 | ||||||
chr12:65922704
|
G | A | 193 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(190): Show | 193 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.250-28679G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922704 | ||||||
chr12:65922891
|
G | A | 18 | a0001c0001t0003g0190a0001c0001t0004g0076a0001c0001t0006g0003others(15): Show | 18 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.250-28492G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922891 | ||||||
chr12:65923118
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.250-28265G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923118 | ||||||
chr12:65923133
|
A | C | 2 | a0001c0001t0006g0004a0001c0001t0051g0176 | 2 | HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.250-28250A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923133 | ||||||
chr12:65923359
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.250-28024C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923359 | ||||||
chr12:65923425
|
T | G | 1 | a0001c0001t0053g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.250-27958T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923425 | ||||||
chr12:65923707
|
C | A | 6 | a0001c0001t0019g0207a0001c0001t0019g0209a0001c0001t0019g0211others(3): Show | 6 | HG01069.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-27676C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923707 | ||||||
chr12:65923721
|
T | A | 4 | a0001c0001t0098g0030a0001c0001t0112g0224a0001c0001t0130g0226others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-27662T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923721 | ||||||
chr12:65923757
|
C | A | 9 | a0001c0001t0003g0190a0001c0001t0019g0207a0001c0001t0019g0209others(6): Show | 9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-27626C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923757 | ||||||
chr12:65923795
|
G | A | 44 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(41): Show | 44 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.250-27588G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923795 | ||||||
chr12:65923808
|
G | A | 1 | a0001c0001t0021g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.250-27575G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923808 | ||||||
chr12:65924178
|
C | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-27205C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924178 | ||||||
chr12:65924368
|
C | T | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-27015C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924368 | ||||||
chr12:65924437
|
C | T | 3 | a0001c0001t0061g0079a0001c0001t0065g0081a0001c0001t0090g0078 | 3 | HG01074.hp1 HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.250-26946C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924437 | ||||||
chr12:65924450
|
T | TAC | 4 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-26917_250-2691 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65924450 | |||||
chr12:65924454
|
C | T | 2 | a0001c0001t0056g0116a0001c0001t0133g0087 | 2 | HG02027.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.250-26929C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924454 | ||||||
chr12:65924669
|
G | A | 1 | a0001c0001t0004g0025 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.250-26714G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924669 | ||||||
chr12:65924791
|
C | G | 2 | a0001c0001t0002g0060a0001c0001t0128g0189 | 2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.250-26592C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924791 | ||||||
chr12:65924929
|
T | C | 2 | a0001c0001t0011g0066a0001c0001t0011g0067 | 2 | NA18970.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.250-26454T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924929 | ||||||
chr12:65925404
|
A | C | 4 | a0001c0001t0018g0223a0001c0001t0045g0050a0001c0001t0045g0055others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-25979A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925404 | ||||||
chr12:65925653
|
A | G | 6 | a0001c0001t0003g0009a0001c0001t0104g0216a0001c0001t0115g0007others(3): Show | 6 | HG01361.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-25730A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925653 | ||||||
chr12:65925719
|
T | C | 4 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0110g0182others(1): Show | 4 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-25664T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925719 | ||||||
chr12:65925755
|
A | G | 1 | a0001c0001t0018g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-25628A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925755 | ||||||
chr12:65925777
|
C | CG | 88 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(85): Show | 88 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.250-25603dupG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65925777 | |||||
chr12:65925905
|
T | C | 1 | a0001c0001t0095g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.250-25478T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925905 | ||||||
chr12:65926094
|
T | A | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-25289T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926094 | ||||||
chr12:65926095
|
A | T | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-25288A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926095 | ||||||
chr12:65926216
|
A | C | 84 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(81): Show | 84 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.250-25167A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926216 | ||||||
chr12:65926510
|
T | A | 1 | a0001c0001t0066g0135 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.250-24873T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926510 | ||||||
chr12:65926680
|
A | G | 4 | a0001c0001t0098g0030a0001c0001t0112g0224a0001c0001t0130g0226others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-24703A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926680 | ||||||
chr12:65926978
|
T | C | 1 | a0001c0001t0005g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250-24405T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926978 | ||||||
chr12:65927041
|
G | A | 9 | a0001c0001t0003g0190a0001c0001t0019g0207a0001c0001t0019g0209others(6): Show | 9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-24342G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927041 | ||||||
chr12:65927093
|
G | A | 84 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(81): Show | 84 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.250-24290G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927093 | ||||||
chr12:65927111
|
A | G | 45 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(42): Show | 45 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.250-24272A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927111 | ||||||
chr12:65927114
|
G | A | 43 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(40): Show | 43 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.250-24269G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927114 | ||||||
chr12:65927145
|
C | T | 1 | a0001c0001t0037g0141 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.250-24238C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927145 | ||||||
chr12:65927564
|
C | G | 84 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(81): Show | 84 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.250-23819C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927564 | ||||||
chr12:65927566
|
C | T | 17 | a0001c0001t0004g0025a0001c0001t0004g0074a0001c0001t0006g0197others(14): Show | 17 | HG00423.hp2 HG01192.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.250-23817C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927566 | ||||||
chr12:65927692
|
T | A | 2 | a0001c0001t0005g0053a0001c0001t0049g0186 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-23691T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927692 | ||||||
chr12:65927712
|
T | C | 88 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(85): Show | 88 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.250-23671T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927712 | ||||||
chr12:65927831
|
C | CTG | 70 | a0001c0001t0004g0025a0001c0001t0004g0038a0001c0001t0004g0058others(67): Show | 70 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.250-23532_250-2353 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | |||||
chr12:65927831
|
C | CTGTG | 15 | a0001c0001t0003g0009a0001c0001t0006g0197a0001c0001t0006g0198others(12): Show | 15 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.250-23534_250-2353 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | |||||
chr12:65927831
|
C | CTGTGTG | 76 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(73): Show | 76 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.250-23536_250-2353 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | |||||
chr12:65927831
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0011g0027a0001c0001t0011g0049 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-23540_250-2353 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | |||||
chr12:65927853
|
A | G | 88 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(85): Show | 88 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.250-23530A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927853 | ||||||
chr12:65927891
|
G | A | 32 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.250-23492G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927891 | ||||||
chr12:65927949
|
GTA | G | 16 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0065others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.250-23418_250-2341 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927949 | |||||
chr12:65927949
|
GTATA | G | 75 | a0001c0001t0004g0025a0001c0001t0004g0038a0001c0001t0004g0058others(72): Show | 75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.250-23420_250-2341 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927949 | |||||
chr12:65927949
|
GTATATA | G | 87 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(84): Show | 87 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.250-23422_250-2341 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927949 | |||||
chr12:65927964
|
T | C | 75 | a0001c0001t0004g0025a0001c0001t0004g0038a0001c0001t0004g0058others(72): Show | 75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.250-23419T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927964 | ||||||
chr12:65928160
|
C | T | 3 | a0001c0001t0045g0050a0001c0001t0045g0055a0001c0001t0080g0048 | 3 | HG02647.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.250-23223C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928160 | ||||||
chr12:65928181
|
C | T | 1 | a0001c0001t0099g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-23202C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928181 | ||||||
chr12:65928275
|
C | T | 2 | a0001c0001t0011g0027a0001c0001t0011g0049 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-23108C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928275 | ||||||
chr12:65928319
|
T | C | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-23064T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928319 | ||||||
chr12:65928542
|
C | A | 83 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(80): Show | 83 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.250-22841C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928542 | ||||||
chr12:65929011
|
C | A | 1 | a0001c0001t0028g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.250-22372C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929011 | ||||||
chr12:65929061
|
G | A | 32 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.250-22322G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929061 | ||||||
chr12:65929304
|
G | T | 1 | a0001c0001t0115g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250-22079G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929304 | ||||||
chr12:65929429
|
C | G | 1 | a0001c0001t0012g0130 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.250-21954C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929429 | ||||||
chr12:65929609
|
A | G | 1 | a0001c0001t0010g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.250-21774A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929609 | ||||||
chr12:65929629
|
A | C | 1 | a0001c0001t0050g0145 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.250-21754A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929629 | ||||||
chr12:65929820
|
T | C | 1 | a0001c0001t0003g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.250-21563T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929820 | ||||||
chr12:65929930
|
G | T | 1 | a0001c0001t0044g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.250-21453G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929930 | ||||||
chr12:65929939
|
C | T | 2 | a0001c0001t0004g0076a0001c0001t0053g0010 | 2 | HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.250-21444C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929939 | ||||||
chr12:65930096
|
T | C | 3 | a0001c0001t0034g0126a0001c0001t0073g0165a0001c0001t0089g0083 | 3 | HG00741.hp2 HG01433.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.250-21287T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930096 | ||||||
chr12:65930107
|
G | A | 1 | a0001c0001t0008g0090 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.250-21276G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930107 | ||||||
chr12:65930187
|
A | G | 2 | a0001c0001t0003g0213a0001c0001t0003g0214 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.250-21196A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930187 | ||||||
chr12:65930327
|
C | T | 2 | a0001c0001t0007g0021a0001c0001t0007g0022 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.250-21056C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930327 | ||||||
chr12:65930387
|
C | T | 2 | a0001c0001t0013g0107a0001c0001t0022g0146 | 2 | HG03831.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.250-20996C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930387 | ||||||
chr12:65930749
|
G | A | 1 | a0001c0001t0028g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.250-20634G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930749 | ||||||
chr12:65930810
|
C | T | 26 | a0001c0001t0002g0060a0001c0001t0005g0014a0001c0001t0005g0015others(23): Show | 26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-20573C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930810 | ||||||
chr12:65931099
|
C | T | 2 | a0001c0001t0015g0149a0001c0001t0087g0086 | 2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.250-20284C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931099 | ||||||
chr12:65931106
|
A | AT | 26 | a0001c0001t0002g0060a0001c0001t0005g0014a0001c0001t0005g0015others(23): Show | 26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-20272dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931106 | |||||
chr12:65931523
|
G | A | 1 | a0001c0001t0061g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250-19860G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931523 | ||||||
chr12:65931528
|
C | G | 2 | a0001c0001t0012g0111a0001c0001t0067g0138 | 2 | NA18952.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.250-19855C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931528 | ||||||
chr12:65931551
|
T | TTG | 16 | a0001c0001t0002g0039a0001c0001t0002g0068a0001c0001t0002g0070others(13): Show | 16 | HG00558.hp2 HG01361.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-19794_250-1979 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
T | TTGTG | 30 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(27): Show | 30 | HG00609.hp1 HG00735.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.250-19796_250-1979 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
T | TTGTGTG | 9 | a0001c0001t0001g0045a0001c0001t0008g0090a0001c0001t0018g0225others(6): Show | 9 | HG01891.hp1 HG02738.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-19798_250-1979 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
T | TTGTGTGT others(1): Show |
26 | a0001c0001t0002g0060a0001c0001t0003g0009a0001c0001t0005g0014others(23): Show | 26 | HG00423.hp1 HG00558.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-19800_250-1979 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0056a0001c0001t0005g0059a0001c0001t0008g0139 | 3 | HG01496.hp1 HG04204.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.250-19802_250-1979 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
TTG | T | 15 | a0001c0001t0006g0004a0001c0001t0009g0124a0001c0001t0014g0112others(12): Show | 15 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.250-19794_250-1979 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
TTGTG | T | 8 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0016g0123others(5): Show | 8 | HG01884.hp2 HG02300.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-19796_250-1979 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
TTGTGTG | T | 74 | a0001c0001t0003g0190a0001c0001t0004g0025a0001c0001t0004g0038others(71): Show | 74 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.250-19798_250-1979 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0009g0085a0001c0001t0086g0217a0001c0001t0104g0216others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-19800_250-1979 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0111g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.250-19802_250-1979 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931551
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0063g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.250-19806_250-1979 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | |||||
chr12:65931730
|
C | T | 1 | a0001c0001t0039g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.250-19653C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931730 | ||||||
chr12:65931909
|
T | C | 33 | a0001c0001t0002g0039a0001c0001t0003g0208a0001c0001t0003g0213others(30): Show | 33 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.250-19474T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931909 | ||||||
chr12:65932063
|
T | C | 75 | a0001c0001t0004g0025a0001c0001t0004g0038a0001c0001t0004g0058others(72): Show | 75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.250-19320T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932063 | ||||||
chr12:65932113
|
G | T | 3 | a0001c0001t0005g0064a0001c0001t0049g0191a0001c0001t0100g0020 | 3 | NA18952.hp1 NA18972.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.250-19270G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932113 | ||||||
chr12:65932224
|
T | C | 1 | a0001c0001t0005g0014 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.250-19159T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932224 | ||||||
chr12:65932359
|
G | A | 57 | a0001c0001t0004g0038a0001c0001t0004g0058a0001c0001t0004g0069others(54): Show | 57 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.250-19024G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932359 | ||||||
chr12:65932479
|
C | T | 1 | a0001c0001t0061g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250-18904C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932479 | ||||||
chr12:65932536
|
T | C | 1 | a0001c0001t0134g0114 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.250-18847T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932536 | ||||||
chr12:65932573
|
T | C | 1 | a0001c0001t0085g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.250-18810T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932573 | ||||||
chr12:65932763
|
A | T | 2 | a0001c0001t0027g0157a0001c0001t0031g0151 | 2 | HG02083.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.250-18620A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932763 | ||||||
chr12:65933154
|
A | G | 4 | a0001c0001t0002g0073a0001c0001t0007g0017a0001c0001t0043g0018others(1): Show | 4 | HG01074.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-18229A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933154 | ||||||
chr12:65933163
|
A | G | 158 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(155): Show | 158 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.250-18220A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933163 | ||||||
chr12:65933248
|
C | T | 26 | a0001c0001t0002g0060a0001c0001t0005g0014a0001c0001t0005g0015others(23): Show | 26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-18135C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933248 | ||||||
chr12:65933367
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250-18016C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933367 | ||||||
chr12:65933403
|
C | T | 2 | a0001c0001t0011g0027a0001c0001t0011g0049 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-17980C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933403 | ||||||
chr12:65933474
|
A | G | 16 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0065others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.250-17909A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933474 | ||||||
chr12:65933801
|
A | T | 4 | a0001c0001t0004g0069a0001c0001t0015g0140a0001c0001t0033g0096others(1): Show | 4 | HG00621.hp2 NA18941.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-17582A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933801 | ||||||
chr12:65933852
|
A | G | 167 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(164): Show | 167 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.250-17531A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933852 | ||||||
chr12:65933875
|
T | C | 3 | a0001c0001t0026g0154a0001c0001t0058g0152a0001c0001t0077g0195 | 3 | HG00621.hp1 HG02165.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.250-17508T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933875 | ||||||
chr12:65934198
|
T | C | 32 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.250-17185T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934198 | ||||||
chr12:65934233
|
A | G | 2 | a0001c0001t0005g0053a0001c0001t0049g0186 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-17150A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934233 | ||||||
chr12:65934247
|
C | T | 83 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(80): Show | 83 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.250-17136C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934247 | ||||||
chr12:65934374
|
T | A | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-17009T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934374 | ||||||
chr12:65934466
|
C | T | 1 | a0001c0001t0134g0114 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.250-16917C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934466 | ||||||
chr12:65934607
|
C | T | 1 | a0001c0001t0018g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-16776C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934607 | ||||||
chr12:65934647
|
T | C | 2 | a0001c0001t0006g0003a0001c0001t0084g0002 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.250-16736T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934647 | ||||||
chr12:65934818
|
A | G | 1 | a0001c0001t0034g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.250-16565A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934818 | ||||||
chr12:65934851
|
C | G | 1 | a0001c0001t0131g0222 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-16532C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934851 | ||||||
chr12:65935086
|
C | T | 12 | a0001c0001t0005g0064a0001c0001t0038g0115a0001c0001t0038g0193others(9): Show | 12 | HG00423.hp1 NA18952.hp1 NA18961.hp1 others(9): Show |
intron_variant | MODIFIER | c.250-16297C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935086 | ||||||
chr12:65935464
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.250-15919G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935464 | ||||||
chr12:65935585
|
A | G | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-15798A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935585 | ||||||
chr12:65935889
|
A | T | 1 | a0001c0001t0004g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250-15494A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935889 | ||||||
chr12:65936212
|
A | AT | 107 | a0001c0001t0002g0039a0001c0001t0002g0060a0001c0001t0002g0061others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.250-15157dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65936212 | |||||
chr12:65936212
|
AT | A | 12 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.250-15157delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65936212 | |||||
chr12:65936421
|
A | C | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-14962A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936421 | ||||||
chr12:65936564
|
T | G | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-14819T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936564 | ||||||
chr12:65936565
|
C | T | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-14818C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936565 | ||||||
chr12:65936938
|
A | T | 1 | a0001c0001t0018g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-14445A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936938 | ||||||
chr12:65937284
|
C | G | 2 | a0001c0001t0011g0027a0001c0001t0011g0049 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-14099C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937284 | ||||||
chr12:65937480
|
G | A | 1 | a0001c0001t0016g0113 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.250-13903G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937480 | ||||||
chr12:65937585
|
G | C | 83 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(80): Show | 83 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.250-13798G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937585 | ||||||
chr12:65937883
|
C | T | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-13500C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937883 | ||||||
chr12:65937908
|
C | T | 1 | a0001c0001t0013g0107 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250-13475C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937908 | ||||||
chr12:65937912
|
G | A | 1 | a0001c0001t0103g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.250-13471G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937912 | ||||||
chr12:65938939
|
C | G | 2 | a0001c0001t0024g0110a0001c0001t0036g0077 | 2 | HG01978.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.250-12444C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65938939 | ||||||
chr12:65939029
|
G | A | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-12354G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939029 | ||||||
chr12:65939166
|
C | T | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-12217C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939166 | ||||||
chr12:65939375
|
A | T | 1 | a0001c0001t0010g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.250-12008A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939375 | ||||||
chr12:65939419
|
G | A | 1 | a0001c0001t0004g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.250-11964G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939419 | ||||||
chr12:65939673
|
G | A | 1 | a0001c0001t0129g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250-11710G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939673 | ||||||
chr12:65939725
|
T | C | 4 | a0001c0001t0098g0030a0001c0001t0112g0224a0001c0001t0130g0226others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-11658T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939725 | ||||||
chr12:65939847
|
G | A | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-11536G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939847 | ||||||
chr12:65939884
|
G | C | 5 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0065others(2): Show | 5 | HG02132.hp1 NA18951.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-11499G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939884 | ||||||
chr12:65939995
|
T | G | 26 | a0001c0001t0002g0060a0001c0001t0005g0014a0001c0001t0005g0015others(23): Show | 26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-11388T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939995 | ||||||
chr12:65940113
|
G | GA | 11 | a0001c0001t0018g0013a0001c0001t0021g0170a0001c0001t0021g0171others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-11261dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65940113 | |||||
chr12:65940246
|
T | C | 5 | a0001c0001t0025g0173a0001c0001t0025g0174a0001c0001t0055g0221others(2): Show | 5 | HG01243.hp1 HG02717.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-11137T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65940246 | ||||||
chr12:65940964
|
C | T | 2 | a0001c0001t0016g0113a0001c0001t0096g0234 | 2 | HG00280.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.250-10419C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65940964 | ||||||
chr12:65941428
|
C | T | 1 | a0001c0001t0052g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.250-9955C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65941428 | ||||||
chr12:65941923
|
T | C | 11 | a0001c0001t0018g0013a0001c0001t0021g0170a0001c0001t0021g0171others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-9460T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65941923 | ||||||
chr12:65941958
|
A | T | 9 | a0001c0001t0003g0190a0001c0001t0019g0207a0001c0001t0019g0209others(6): Show | 9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-9425A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65941958 | ||||||
chr12:65942322
|
T | C | 1 | a0001c0001t0071g0092 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.250-9061T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65942322 | ||||||
chr12:65942912
|
C | T | 32 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.250-8471C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65942912 | ||||||
chr12:65942986
|
G | A | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-8397G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65942986 | ||||||
chr12:65943232
|
T | G | 1 | a0001c0001t0042g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.250-8151T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943232 | ||||||
chr12:65943246
|
A | G | 1 | a0001c0001t0087g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.250-8137A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943246 | ||||||
chr12:65943413
|
A | G | 1 | a0001c0001t0128g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.250-7970A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943413 | ||||||
chr12:65943436
|
A | T | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-7947A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943436 | ||||||
chr12:65943462
|
G | C | 3 | a0001c0001t0027g0157a0001c0001t0031g0151a0002c0002t0020g0099 | 3 | HG02027.hp1 HG02083.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.250-7921G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943462 | ||||||
chr12:65943864
|
G | A | 1 | a0001c0001t0070g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.250-7519G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943864 | ||||||
chr12:65943902
|
C | T | 1 | a0001c0001t0038g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250-7481C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943902 | ||||||
chr12:65944422
|
G | T | 78 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(75): Show | 78 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.250-6961G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944422 | ||||||
chr12:65944651
|
A | AC | 83 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(80): Show | 83 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.250-6730dupC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65944651 | |||||
chr12:65944698
|
CA | C | 2 | a0001c0001t0013g0153a0001c0001t0013g0156 | 2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.250-6684delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944698 | ||||||
chr12:65944710
|
C | T | 1 | a0001c0001t0109g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-6673C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944710 | ||||||
chr12:65944802
|
C | T | 2 | a0001c0001t0046g0169a0001c0001t0105g0168 | 2 | HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.250-6581C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944802 | ||||||
chr12:65944898
|
T | TTGCCCAT others(10): Show |
5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-6484_250-6468d others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65944898 | |||||
chr12:65945126
|
G | A | 1 | a0001c0001t0045g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.250-6257G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65945126 | ||||||
chr12:65945235
|
TA | T | 9 | a0001c0001t0007g0021a0001c0001t0007g0022a0001c0001t0021g0170others(6): Show | 9 | HG00733.hp1 HG01070.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-6134delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65945235 | |||||
chr12:65945354
|
C | A | 5 | a0001c0001t0018g0223a0001c0001t0045g0050a0001c0001t0045g0055others(2): Show | 5 | HG02647.hp1 HG03041.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-6029C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65945354 | ||||||
chr12:65946087
|
G | A | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-5296G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946087 | ||||||
chr12:65946228
|
A | G | 1 | a0001c0001t0003g0208 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.250-5155A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946228 | ||||||
chr12:65946506
|
T | A | 26 | a0001c0001t0002g0060a0001c0001t0005g0014a0001c0001t0005g0015others(23): Show | 26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-4877T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946506 | ||||||
chr12:65946588
|
G | C | 1 | a0001c0001t0078g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-4795G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946588 | ||||||
chr12:65946923
|
A | C | 82 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(79): Show | 82 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.250-4460A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946923 | ||||||
chr12:65946993
|
T | C | 11 | a0001c0001t0018g0013a0001c0001t0021g0170a0001c0001t0021g0171others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-4390T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946993 | ||||||
chr12:65947124
|
T | C | 1 | a0001c0001t0038g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250-4259T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947124 | ||||||
chr12:65947144
|
G | A | 1 | a0001c0001t0076g0205 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.250-4239G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947144 | ||||||
chr12:65947209
|
T | G | 1 | a0001c0001t0063g0164 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.250-4174T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947209 | ||||||
chr12:65947255
|
G | A | 10 | a0001c0001t0003g0190a0001c0001t0019g0207a0001c0001t0019g0209others(7): Show | 10 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-4128G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947255 | ||||||
chr12:65947269
|
G | A | 2 | a0001c0001t0048g0199a0001c0001t0048g0215 | 2 | NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.250-4114G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947269 | ||||||
chr12:65947542
|
T | C | 1 | a0001c0001t0086g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-3841T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947542 | ||||||
chr12:65947546
|
A | T | 1 | a0001c0001t0013g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.250-3837A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947546 | ||||||
chr12:65947729
|
A | G | 1 | a0001c0001t0078g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-3654A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947729 | ||||||
chr12:65947804
|
G | A | 1 | a0001c0001t0010g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.250-3579G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947804 | ||||||
chr12:65947822
|
G | A | 4 | a0001c0001t0098g0030a0001c0001t0112g0224a0001c0001t0130g0226others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-3561G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947822 | ||||||
chr12:65947944
|
A | G | 1 | a0001c0001t0048g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.250-3439A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947944 | ||||||
chr12:65948093
|
C | T | 16 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0059others(13): Show | 16 | HG00423.hp1 HG04204.hp1 NA18952.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-3290C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948093 | ||||||
chr12:65948333
|
A | T | 1 | a0001c0001t0013g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.250-3050A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948333 | ||||||
chr12:65948337
|
G | A | 16 | a0001c0001t0003g0190a0001c0001t0019g0207a0001c0001t0019g0209others(13): Show | 16 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-3046G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948337 | ||||||
chr12:65948447
|
G | A | 2 | a0001c0001t0055g0221a0001c0001t0101g0043 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.250-2936G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948447 | ||||||
chr12:65948481
|
T | G | 1 | a0001c0001t0056g0116 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.250-2902T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948481 | ||||||
chr12:65948824
|
G | A | 1 | a0001c0001t0073g0165 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.250-2559G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948824 | ||||||
chr12:65949088
|
C | T | 17 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0059others(14): Show | 17 | HG00423.hp1 HG03017.hp2 HG04204.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-2295C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65949088 | ||||||
chr12:65949452
|
G | T | 1 | a0001c0001t0012g0131 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.250-1931G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65949452 | ||||||
chr12:65949620
|
G | C | 167 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(164): Show | 167 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.250-1763G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65949620 | ||||||
chr12:65950030
|
C | T | 166 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(163): Show | 166 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.250-1353C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950030 | ||||||
chr12:65950070
|
C | T | 2 | a0001c0001t0005g0053a0001c0001t0049g0186 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-1313C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950070 | ||||||
chr12:65950114
|
C | A | 3 | a0001c0001t0014g0112a0001c0001t0014g0142a0001c0001t0085g0143 | 3 | HG01167.hp2 HG01261.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.250-1269C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950114 | ||||||
chr12:65950926
|
A | G | 6 | a0001c0001t0019g0207a0001c0001t0019g0209a0001c0001t0019g0211others(3): Show | 6 | HG01069.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-457A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950926 | ||||||
chr12:65951262
|
T | C | 1 | a0001c0001t0026g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.250-121T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65951262 | ||||||
chr12:65951424
|
T | C | 1 | a0001c0001t0120g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.282+9T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65951424 | ||||||
chr12:65951605
|
C | G | 1 | a0001c0001t0042g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.282+190C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65951605 | ||||||
chr12:65952313
|
C | A | 1 | a0001c0001t0034g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.282+898C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952313 | ||||||
chr12:65952341
|
A | G | 84 | a0001c0001t0004g0025a0001c0001t0004g0038a0001c0001t0004g0058others(81): Show | 84 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.282+926A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952341 | ||||||
chr12:65952427
|
T | C | 2 | a0001c0001t0021g0170a0001c0001t0021g0171 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.282+1012T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952427 | ||||||
chr12:65952589
|
TA | T | 5 | a0001c0001t0098g0030a0001c0001t0109g0012a0001c0001t0112g0224others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+1182delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65952589 | |||||
chr12:65952844
|
T | C | 154 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(151): Show | 154 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.282+1429T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952844 | ||||||
chr12:65952934
|
T | C | 16 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+1519T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952934 | ||||||
chr12:65953080
|
A | G | 1 | a0001c0001t0129g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.282+1665A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953080 | ||||||
chr12:65953149
|
C | A | 1 | a0001c0001t0018g0225 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.282+1734C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953149 | ||||||
chr12:65953239
|
T | C | 1 | a0001c0001t0018g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.282+1824T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953239 | ||||||
chr12:65953257
|
T | C | 1 | a0001c0001t0060g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.282+1842T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953257 | ||||||
chr12:65953270
|
G | A | 1 | a0001c0001t0047g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.282+1855G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953270 | ||||||
chr12:65953384
|
T | G | 7 | a0001c0001t0017g0194a0001c0001t0024g0110a0001c0001t0036g0077others(4): Show | 7 | HG00609.hp2 HG00735.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1969T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953384 | ||||||
chr12:65953422
|
C | T | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+2007C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953422 | ||||||
chr12:65953458
|
G | A | 2 | a0001c0001t0011g0027a0001c0001t0011g0049 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.282+2043G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953458 | ||||||
chr12:65953588
|
G | T | 165 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(162): Show | 165 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.282+2173G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953588 | ||||||
chr12:65953593
|
T | C | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+2178T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953593 | ||||||
chr12:65953657
|
C | G | 10 | a0001c0001t0009g0104a0001c0001t0017g0102a0001c0001t0017g0105others(7): Show | 10 | HG01361.hp1 HG01496.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.282+2242C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953657 | ||||||
chr12:65953914
|
T | C | 2 | a0001c0001t0011g0027a0001c0001t0011g0049 | 2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.282+2499T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953914 | ||||||
chr12:65954090
|
A | C | 83 | a0001c0001t0004g0025a0001c0001t0004g0038a0001c0001t0004g0058others(80): Show | 83 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.282+2675A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954090 | ||||||
chr12:65954157
|
C | G | 1 | a0001c0001t0056g0116 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.282+2742C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954157 | ||||||
chr12:65954354
|
T | A | 32 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.282+2939T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954354 | ||||||
chr12:65954600
|
C | A | 5 | a0001c0001t0098g0030a0001c0001t0109g0012a0001c0001t0112g0224others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+3185C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954600 | ||||||
chr12:65954889
|
T | C | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+3474T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954889 | ||||||
chr12:65954943
|
A | G | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+3528A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954943 | ||||||
chr12:65955010
|
A | G | 44 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0035others(41): Show | 44 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.282+3595A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955010 | ||||||
chr12:65955022
|
T | C | 1 | a0001c0001t0039g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.282+3607T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955022 | ||||||
chr12:65955041
|
C | T | 1 | a0001c0001t0108g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.282+3626C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955041 | ||||||
chr12:65955046
|
C | T | 4 | a0001c0001t0002g0073a0001c0001t0007g0017a0001c0001t0043g0018others(1): Show | 4 | HG01074.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+3631C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955046 | ||||||
chr12:65955251
|
A | G | 1 | a0001c0001t0008g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.282+3836A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955251 | ||||||
chr12:65955306
|
TA | T | 3 | a0001c0001t0005g0059a0001c0001t0047g0185a0001c0001t0083g0088 | 3 | NA18991.hp2 NA19030.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.282+3898delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65955306 | |||||
chr12:65955315
|
A | C | 1 | a0001c0001t0093g0095 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.282+3900A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955315 | ||||||
chr12:65955655
|
A | G | 1 | a0001c0001t0077g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.282+4240A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955655 | ||||||
chr12:65955679
|
A | G | 1 | a0001c0001t0116g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.282+4264A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955679 | ||||||
chr12:65955726
|
G | A | 1 | a0001c0001t0129g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.282+4311G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955726 | ||||||
chr12:65956012
|
G | A | 4 | a0001c0001t0023g0132a0001c0001t0037g0201a0001c0001t0056g0116others(1): Show | 4 | HG02027.hp2 NA18943.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+4597G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956012 | ||||||
chr12:65956032
|
A | G | 32 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.282+4617A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956032 | ||||||
chr12:65956063
|
TCACTCTA others(1): Show |
T | 26 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0035others(23): Show | 26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+4654_282+4661d others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65956063 | |||||
chr12:65956146
|
C | T | 4 | a0001c0001t0098g0030a0001c0001t0112g0224a0001c0001t0130g0226others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4731C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956146 | ||||||
chr12:65956320
|
C | T | 3 | a0001c0001t0003g0009a0001c0001t0115g0007a0001c0001t0119g0008 | 3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.282+4905C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956320 | ||||||
chr12:65956691
|
C | T | 5 | a0001c0001t0098g0030a0001c0001t0109g0012a0001c0001t0112g0224others(2): Show | 5 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+5276C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956691 | ||||||
chr12:65956744
|
G | T | 1 | a0001c0001t0056g0116 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.282+5329G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956744 | ||||||
chr12:65956850
|
G | A | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+5435G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956850 | ||||||
chr12:65956938
|
G | A | 1 | a0001c0001t0111g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.282+5523G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956938 | ||||||
chr12:65957337
|
G | A | 26 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0035others(23): Show | 26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-5908G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957337 | ||||||
chr12:65957361
|
C | T | 6 | a0001c0001t0006g0228a0001c0001t0026g0097a0001c0001t0026g0154others(3): Show | 6 | HG00621.hp1 HG02165.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-5884C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957361 | ||||||
chr12:65957515
|
T | C | 1 | a0001c0001t0130g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283-5730T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957515 | ||||||
chr12:65957609
|
C | T | 5 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-5636C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957609 | ||||||
chr12:65957688
|
C | G | 2 | a0001c0001t0021g0170a0001c0001t0021g0171 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.283-5557C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957688 | ||||||
chr12:65957725
|
C | T | 2 | a0001c0001t0044g0051a0001c0001t0044g0052 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.283-5520C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957725 | ||||||
chr12:65957763
|
A | G | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-5482A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957763 | ||||||
chr12:65957932
|
A | G | 1 | a0001c0001t0111g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.283-5313A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957932 | ||||||
chr12:65958000
|
C | CT | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-5245_283-5244i others(3): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958000 | ||||||
chr12:65958038
|
T | C | 44 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0035others(41): Show | 44 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.283-5207T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958038 | ||||||
chr12:65958046
|
T | C | 176 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(173): Show | 176 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.283-5199T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958046 | ||||||
chr12:65958371
|
G | A | 18 | a0001c0001t0004g0025a0001c0001t0004g0074a0001c0001t0006g0197others(15): Show | 18 | HG00423.hp2 HG01192.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-4874G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958371 | ||||||
chr12:65958406
|
A | G | 1 | a0001c0001t0008g0090 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.283-4839A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958406 | ||||||
chr12:65958792
|
C | T | 31 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0035others(28): Show | 31 | HG00423.hp1 HG01884.hp2 HG02559.hp2 others(28): Show |
intron_variant | MODIFIER | c.283-4453C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958792 | ||||||
chr12:65958914
|
G | A | 1 | a0001c0001t0004g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283-4331G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958914 | ||||||
chr12:65958981
|
G | C | 9 | a0001c0001t0004g0069a0001c0001t0006g0204a0001c0001t0010g0057others(6): Show | 9 | HG00621.hp2 HG00673.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-4264G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958981 | ||||||
chr12:65959496
|
C | T | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-3749C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959496 | ||||||
chr12:65959507
|
T | C | 1 | a0001c0001t0079g0117 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.283-3738T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959507 | ||||||
chr12:65959893
|
T | C | 1 | a0001c0001t0024g0155 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.283-3352T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959893 | ||||||
chr12:65959959
|
G | A | 1 | a0001c0001t0060g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.283-3286G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959959 | ||||||
chr12:65960075
|
G | C | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-3170G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960075 | ||||||
chr12:65960111
|
G | A | 114 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(111): Show | 114 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.283-3134G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960111 | ||||||
chr12:65960131
|
C | T | 1 | a0001c0001t0062g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.283-3114C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960131 | ||||||
chr12:65960220
|
T | C | 1 | a0001c0001t0012g0130 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283-3025T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960220 | ||||||
chr12:65960278
|
G | A | 4 | a0001c0001t0098g0030a0001c0001t0112g0224a0001c0001t0130g0226others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-2967G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960278 | ||||||
chr12:65960375
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283-2870A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960375 | ||||||
chr12:65960442
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | NA18948.hp2 NA18957.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.283-2803T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960442 | ||||||
chr12:65960632
|
T | A | 2 | a0001c0001t0005g0053a0001c0001t0049g0186 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.283-2613T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960632 | ||||||
chr12:65960845
|
T | A | 1 | a0001c0001t0047g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-2400T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960845 | ||||||
chr12:65961118
|
C | T | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-2127C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961118 | ||||||
chr12:65961131
|
G | A | 136 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(133): Show | 136 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.283-2114G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961131 | ||||||
chr12:65961168
|
C | T | 30 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0035others(27): Show | 30 | HG00423.hp1 HG01884.hp2 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.283-2077C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961168 | ||||||
chr12:65961169
|
G | A | 9 | a0001c0001t0003g0190a0001c0001t0019g0207a0001c0001t0019g0209others(6): Show | 9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-2076G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961169 | ||||||
chr12:65961206
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283-2039C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961206 | ||||||
chr12:65961238
|
C | A | 4 | a0001c0001t0002g0073a0001c0001t0007g0017a0001c0001t0043g0018others(1): Show | 4 | HG01074.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2007C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961238 | ||||||
chr12:65961511
|
G | A | 1 | a0001c0001t0064g0016 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.283-1734G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961511 | ||||||
chr12:65961547
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.283-1698C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961547 | ||||||
chr12:65961567
|
A | G | 13 | a0001c0001t0011g0027a0001c0001t0011g0049a0001c0001t0018g0013others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-1678A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961567 | ||||||
chr12:65961738
|
A | AGT | 4 | a0001c0001t0009g0085a0001c0001t0098g0030a0001c0001t0112g0224others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-1488_283-1487d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65961738 | |||||
chr12:65961738
|
AGT | A | 31 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0032others(28): Show | 31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.283-1488_283-1487d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65961738 | |||||
chr12:65961738
|
AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0047g0183a0001c0001t0047g0185a0001c0001t0086g0217others(4): Show | 7 | HG01361.hp2 HG02258.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1494_283-1487d others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65961738 | |||||
chr12:65962235
|
T | C | 1 | a0001c0001t0005g0059 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.283-1010T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962235 | ||||||
chr12:65962320
|
G | A | 75 | a0001c0001t0004g0025a0001c0001t0004g0038a0001c0001t0004g0058others(72): Show | 75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.283-925G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962320 | ||||||
chr12:65962352
|
A | G | 8 | a0001c0001t0018g0013a0001c0001t0025g0173a0001c0001t0025g0174others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-893A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962352 | ||||||
chr12:65962428
|
T | G | 1 | a0001c0001t0104g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-817T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962428 | ||||||
chr12:65962807
|
G | A | 4 | a0001c0001t0098g0030a0001c0001t0112g0224a0001c0001t0130g0226others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-438G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962807 | ||||||
chr12:65962859
|
A | AT | 8 | a0001c0001t0018g0013a0001c0001t0025g0173a0001c0001t0025g0174others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-381dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65962859 | |||||
chr12:65963033
|
A | G | 1 | a0001c0001t0053g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.283-212A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65963033 | ||||||
chr12:65963102
|
A | G | 1 | a0001c0001t0036g0098 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.283-143A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65963102 | ||||||
chr12:65963220
|
T | C | 11 | a0001c0001t0018g0013a0001c0001t0021g0170a0001c0001t0021g0171others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-25T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65963220 |