chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5162158099162158100AG28GENIChomozygous807622600
5162158644162158645CT57GENICpossibly homozygous807622601
5162158647162158648AG53GENIChomozygous807622602
5162158648162158649CT55GENICpossibly homozygous807622603
5162158727162158728CT60GENIChomozygous807622604
5162159839162159840GA21GENIChomozygous807622605
5162162214162162215CT59GENIChomozygous807622606
5162162883162162884AG37GENIChomozygous807622607
5162164718162164719TC38GENIChomozygous807622608