chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145284779145284780GT49GENICpossibly homozygous112870747
4145286112145286113CA44GENIChomozygous112870748
4145286446145286447GA61GENIChomozygous112870749
4145288973145288974CT20GENIChomozygous112870750