chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145414554145414555CT10GENIChomozygous112870863
4145414901145414902CA17GENIChomozygous112870864
4145423225145423226AG22GENIChomozygous112870866
4145424668145424669AG21GENICpossibly homozygous112870868
4145424883145424884TA14GENIChomozygous112870869
4145425213145425214TC18GENIChomozygous112870870
4145425443145425444AG10GENIChomozygous112870871