chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154250124142501242TC15GENIChomozygous119034195
154250136142501362AG9GENIChomozygous129315449
154250179742501798AG7GENIChomozygous129315452
154250451742504518TC48GENIChomozygous112493698
154250767242507673AG40GENIChomozygous112493712
154251056142510562TC49GENIChomozygous112673126
154251139942511400TA52GENIChomozygous112673128
154251202942512030TC44GENIChomozygous112493725
154251249842512499AC46GENIChomozygous112493729
154251473342514734AT33GENIChomozygous112673130
154251562542515626TA53GENIChomozygous112493737
154251569742515698AG52GENIChomozygous112493739
154251730642517307GC40GENIChomozygous112493741
154251795942517960A51GENICpossibly homozygous129250632
154251327942513280A37GENICpossibly homozygous129250626