chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
397928299792830AG57GENIChomozygous111443612
397932079793208TC44GENIChomozygous111443613
397932479793248CT49GENIChomozygous111443614
397933039793304TG63GENIChomozygous111443615
397942289794229TG55GENIChomozygous111443616
397942629794263GA52GENIChomozygous111443617
397944439794444AG45GENIChomozygous111443618
397944609794461CT43GENIChomozygous111443619
397947469794747TC51GENIChomozygous111443620
397947569794757TC46GENIChomozygous111443621
397949039794904TC45GENIChomozygous111443622
397950649795065CT54GENIChomozygous111443623
397950999795100CA51GENIChomozygous111443624
397953779795378TC29GENIChomozygous111443625
397954429795443CT34GENIChomozygous111443626
397954799795480CT37GENIChomozygous111443627
397954899795490CG38GENIChomozygous111443628
397955329795533GA43GENIChomozygous111443629
397962729796273TC49GENIChomozygous111443630
397962969796297AT53GENIChomozygous111443631
397963839796384GA63GENIChomozygous111443632
397965629796563TG45GENIChomozygous111443633
397966089796609AG43GENIChomozygous111443634
397969129796913GT59GENIChomozygous111443635
397970879797088TC48GENIChomozygous111443636
397972039797204GA50GENIChomozygous111443637
397973399797340CT51GENICpossibly homozygous111443638
397974879797488AG41GENIChomozygous111443639
397981469798147CT43GENIChomozygous111443640
397983489798349AC52GENIChomozygous111443641
397986339798634CG47GENIChomozygous111443642
397987149798715AG54GENIChomozygous111443643
397987779798778CT50GENIChomozygous111443644
397935919793592C52GENIChomozygous127848647
397967649796764C65GENIChomozygous127848648
397975569797559ATC33GENIChomozygous127848649