chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162082586820825869CT29GENICpossibly homozygous111753629
162082904420829045GA27GENIChomozygous111753641
162083148620831487TC16GENIChomozygous111753643
162083206420832065CA37GENIChomozygous111753645
162083902220839023CT19GENIChomozygous111753647
162083925320839254AG23GENIChomozygous111753649
162083941320839414GA31GENIChomozygous111753652
162083980320839804GA25GENIChomozygous111753654
162084010820840109AG23GENIChomozygous111753656
162084364920843650CG18GENIChomozygous111753658
162084539120845392GC16GENIChomozygous111753660