chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109446741194467412AG28GENICpossibly homozygous116906916
109446810694468107TC37GENICpossibly homozygous116954927
109446837094468371GA62GENIChomozygous116954929
109447025394470254CT54GENIChomozygous116954931
109447154194471542AG39GENIChomozygous116685300
109447268094472681AG48GENIChomozygous116685306
109447307594473076CA52GENIChomozygous116954933
109447341894473419GA49GENIChomozygous116954935
109447726794477268CA32GENIChomozygous116954937