chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161909741119097412GA15GENIChomozygous998601740
161909779819097799CT16GENIChomozygous998601741
161909817519098176GT21GENIChomozygous998601742
161909930319099304TA26GENIChomozygous998601743
161909955919099560AG23GENIChomozygous998601744
161909977219099773TC23GENIChomozygous998601745
161909983319099834TC18GENIChomozygous998601746
161910003619100037AG26GENIChomozygous998601747
161910008019100081CT27GENIChomozygous998601748
161910008119100082AG26GENIChomozygous998601749
161910156819101569GA22GENIChomozygous998601750
161910184519101846TC28GENIChomozygous998601751
161910240919102410AT20GENIChomozygous998601752
161910255019102551TG25GENIChomozygous998601753
161910344019103441CA19GENIChomozygous998601754
161910478119104782TC21GENIChomozygous998601755
161910622119106222GA9GENIChomozygous998601756
161910622619106227GA9GENIChomozygous998601757
161910692819106929GA27GENIChomozygous998601758
161910791819107919CT18GENIChomozygous998601759
161911547419115475TC24GENIChomozygous998601760
161911986819119869TC21GENIChomozygous998601761
161912400419124005GC22GENIChomozygous998601762