chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47165241471652415GC66GENIChomozygous112706714
47165265571652656CT48GENIChomozygous112706716
47165285071652851CT61GENIChomozygous112706718
47165356871653568G39GENIChomozygous128047732
47165476671654767GC46GENIChomozygous112706720
47165588671655887CT57GENIChomozygous112706722
47165605371656054GA25GENIChomozygous112706724
47165683771656838TC57GENIChomozygous112706726
47165761771657618AT57GENIChomozygous112706728
47165899271658993CA46GENIChomozygous112706730
47166010771660108AT45GENICpossibly homozygous112706732
47166044671660447AG52GENICpossibly homozygous112706734
47166365771663658TC53GENIChomozygous112706736
47166379671663797AG52GENIChomozygous112706738
47166530071665301GT56GENICpossibly homozygous112706740
47166573971665752ACCCCAATTGTAT57GENIChomozygous128047734
47166601871666019CT51GENIChomozygous112706742
47166736471667365TC63GENIChomozygous112706744
47166888971668907GTTATATACGTTTCCCTG52GENIChomozygous128047735
47166971271669713AG51GENIChomozygous112706746