chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101410663914106640AG51GENICpossibly homozygous116736717
101410717614107177AG42GENIChomozygous116736718
101410766014107661AT51GENICpossibly homozygous116736719
101410770814107709AG50GENIChomozygous116736720
101410906514109066AC22GENICpossibly homozygous116859645
101411127714111278GA57GENICpossibly homozygous116736721
101411134414111345CG64GENIChomozygous116736722
101410918814109189AG50GENICpossibly homozygous116994680