chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139080991990809920AT18GENIChomozygous976918665
139081012190810122CG25GENIChomozygous976918666
139081061090810611CT15GENIChomozygous976918667
139081259890812599GC5GENICheterozygous976918668
139081347090813471AG3GENIChomozygous976918669
139081481790814818AG18GENIChomozygous976918670
139081655090816551AG9GENIChomozygous976918671
139081820890818209GA8GENIChomozygous976918672
139082126790821268GA16GENIChomozygous976918673
139082452590824526AT10GENICpossibly homozygous976918674
139082457890824579GT13GENIChomozygous976918675
139082527390825274AG10GENIChomozygous976918676
139082550690825507GA10GENIChomozygous976918677
139082556690825567CT10GENIChomozygous976918678
139082602590826026TC18GENIChomozygous976918679
139082639890826399GT9GENIChomozygous976918680
139082665990826660AG12GENIChomozygous976918681
139082741990827420GA15GENIChomozygous976918682
139082852890828529AG24GENIChomozygous976918683
139082906690829067AG15GENIChomozygous976918684
139083060590830606TC18GENIChomozygous976918685