chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31871151618711517GA25GENIChomozygous136648680
31871153418711535GA25GENIChomozygous136648681
31871374318713744TC24GENIChomozygous136648682
31871491018714911AG18GENIChomozygous136648683
31871870818718709GA16GENIChomozygous136648684
31872052818720529T20GENICpossibly homozygous403570727
31872052818720529TA20GENICheterozygous403570728
31872052918720530T20GENICpossibly homozygous403570729
31872052918720530TA20GENICheterozygous403570730
31872053018720531T20GENICpossibly homozygous403570731
31872053018720531TA20GENICheterozygous403570732
31872194418721945CT20GENIChomozygous136648685
31872252318722524GA16GENIChomozygous136648686
31872368118723682CT13GENIChomozygous136648687
31872394318723944CT17GENIChomozygous136648688
31872509118725092TC15GENIChomozygous136648689
31872558118725582GA15GENIChomozygous136648690
31872560118725602GT16GENIChomozygous136648691
31872563618725637TG14GENIChomozygous136648692
31872575218725753CA18GENIChomozygous136648693
31872601018726011TC11GENIChomozygous136648694
31872635718726358TG17GENIChomozygous136648695