chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
397928299792830AG25GENIChomozygous111443612
397932079793208TC22GENIChomozygous111443613
397932479793248CT21GENIChomozygous111443614
397933039793304TG25GENIChomozygous111443615
397935919793592C16GENIChomozygous127848647
397942289794229TG18GENIChomozygous111443616
397942629794263GA19GENIChomozygous111443617
397944439794444AG19GENIChomozygous111443618
397944609794461CT22GENIChomozygous111443619
397947469794747TC17GENIChomozygous111443620
397947569794757TC17GENIChomozygous111443621
397949039794904TC17GENIChomozygous111443622
397950649795065CT28GENIChomozygous111443623
397950999795100CA27GENIChomozygous111443624
397953779795378TC14GENIChomozygous111443625
397954429795443CT11GENIChomozygous111443626
397954799795480CT13GENIChomozygous111443627
397954899795490CG13GENIChomozygous111443628
397955329795533GA19GENIChomozygous111443629
397962729796273TC21GENIChomozygous111443630
397962969796297AT23GENICpossibly homozygous111443631
397963839796384GA19GENIChomozygous111443632
397965629796563TG18GENIChomozygous111443633
397966089796609AG14GENIChomozygous111443634
397967649796764C17GENIChomozygous127848648
397969129796913GT24GENIChomozygous111443635
397970879797088TC21GENIChomozygous111443636
397972039797204GA18GENIChomozygous111443637
397973399797340CT21GENIChomozygous111443638
397974879797488AG23GENIChomozygous111443639
397975569797559ATC16GENIChomozygous127848649
397987149798715AG16GENIChomozygous111443643
397981469798147CT24GENIChomozygous111443640
397983489798349AC21GENIChomozygous111443641
397986339798634CG16GENIChomozygous111443642
397987779798778CT20GENIChomozygous111443644