chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
397928299792830AG23GENIChomozygous111443612
397932079793208TC16GENIChomozygous111443613
397932479793248CT14GENIChomozygous111443614
397933039793304TG20GENICpossibly homozygous111443615
397942289794229TG23GENIChomozygous111443616
397942629794263GA29GENIChomozygous111443617
397944439794444AG16GENIChomozygous111443618
397944609794461CT15GENIChomozygous111443619
397947469794747TC19GENIChomozygous111443620
397947569794757TC20GENIChomozygous111443621
397949039794904TC25GENIChomozygous111443622
397950649795065CT23GENIChomozygous111443623
397953779795378TC17GENIChomozygous111443625
397954799795480CT23GENIChomozygous111443627
397954899795490CG24GENIChomozygous111443628
397958289795829CT22GENIChomozygous120076907
397962729796273TC19GENIChomozygous111443630
397962969796297AT25GENIChomozygous111443631
397963839796384GA25GENIChomozygous111443632
397965629796563TG19GENIChomozygous111443633
397966089796609AG19GENIChomozygous111443634
397967419796742GA25GENIChomozygous120076908
397967649796764C23GENIChomozygous127848648
397969129796913GT12GENIChomozygous111443635
397970879797088TC23GENIChomozygous111443636
397972039797204GA12GENIChomozygous111443637
397973399797340CT21GENIChomozygous111443638
397974879797488AG18GENIChomozygous111443639
397975569797559ATC15GENIChomozygous127848649
397981469798147CT22GENIChomozygous111443640
397983489798349AC17GENIChomozygous111443641
397986339798634CG12GENIChomozygous111443642
397987149798715AG18GENIChomozygous111443643
397987779798778CT26GENIChomozygous111443644
397980189798018C8GENIChomozygous135259950