chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16415146364151463C76GENIChomozygous131777042
16415205664152057CA64GENIChomozygous109093870
16415239964152400AG62GENIChomozygous109093872
16415331564153316AG71GENIChomozygous109093874
16415331864153319GT70GENIChomozygous109093876
16415390264153903TC78GENIChomozygous109093878
16415539864155398TGTT58GENIChomozygous131777043
16415590764155908CT71GENIChomozygous109093880
16415683064156831AT74GENIChomozygous109093882
16415715064157151GA67GENIChomozygous109093884
16415804064158041GA71GENIChomozygous109093886
16415837664158377TC73GENIChomozygous109093888
16415864464158645CT73GENIChomozygous109093890
16415888964158890CG63GENIChomozygous109093892
16415895164158952GC60GENIChomozygous109093894
16415916164159162AT54GENIChomozygous109093896
16415980464159805CA61GENIChomozygous109093898
16416010564160106CT56GENIChomozygous109093900
16416023064160231TC65GENIChomozygous109093902
16416134164161342TC68GENIChomozygous109093904