chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101545247815452479TG17GENIChomozygous116860320
101545252815452529AG16GENIChomozygous116860322
101545258615452587CT24GENIChomozygous116860324
101545277115452772CA12GENIChomozygous116860326
101545461515454616CT10GENIChomozygous116860328
101545476515454766CT10GENIChomozygous116860330
101545481515454816AG9GENIChomozygous116860332
101545552915455530GA33GENIChomozygous116860334
101545580715455808AT27GENIChomozygous116860336
101545619215456193TC16GENIChomozygous116860338
101545635515456356AG30GENIChomozygous116860340
101545645315456454GA13GENIChomozygous116860342
101545766215457663GA30GENIChomozygous116860344
101545856215458563GT27GENIChomozygous116860346
101545974215459743GA18GENIChomozygous116737812