chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140415502140415503GA31GENIChomozygous115938640
7140418525140418526GA27GENIChomozygous115938641
7140419100140419101TA18GENICpossibly homozygous115938642
7140419396140419397GA22GENIChomozygous115938643
7140420887140420888AG30GENIChomozygous115938644
7140421785140421786TG20GENIChomozygous115938645
7140424781140424782AC27GENIChomozygous115938646
7140424844140424845TA16GENICheterozygous115938647
7140425783140425784CT19GENIChomozygous115938648
7140427082140427083GC26GENIChomozygous115938649
7140427299140427300TC23GENIChomozygous115938650
7140429313140429314GA38GENIChomozygous115938651
7140429661140429662AG18GENIChomozygous115938652
7140429961140429962GT16GENIChomozygous115938653
7140431065140431066AG50GENICheterozygous115938654
7140431627140431628GA28GENIChomozygous115938655
7140432583140432584GC21GENICheterozygous115938656
7140433491140433492CT21GENIChomozygous115938657
7140433766140433767GA15GENICheterozygous115938658
7140436373140436374CT12GENIChomozygous115938659
7140436410140436411TC8GENIChomozygous115938660
7140436676140436677GT17GENIChomozygous115938661