chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43835117138351172TG40GENIChomozygous112591760
43835128238351283GA31GENIChomozygous112591762
43835218138352182CT44GENICpossibly homozygous112591764
43835241438352415TC54GENIChomozygous112591766
43835259938352600CT44GENIChomozygous112591768
43835265238352653GA31GENIChomozygous112591770
43835277438352775GT16GENIChomozygous112591772
43835348238353483GC17GENICpossibly homozygous112591774
43835350638353507CT13GENIChomozygous112591776