chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150269672150269673CT10GENIChomozygous56980615
4150269693150269694TG15GENIChomozygous56980616
4150270255150270256T-7GENIChomozygous58285829
4150270432150270433TA16GENICpossibly homozygous56980618
4150270647150270648CT29GENIChomozygous56980619