chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104676917246769173TC48GENIChomozygous116586604
104676931346769314AC62GENIChomozygous116586606
104677020346770204AG58GENIChomozygous116586608
104677092146770922GC59GENIChomozygous116586610
104677171846771719AG36GENIChomozygous116586612
104677217146772172CT44GENIChomozygous116586614
104677309446773095GA48GENIChomozygous116586616
104677326846773269CT55GENIChomozygous116586618
104677346046773461GC39GENIChomozygous116586620
104677649446776495AT50GENIChomozygous116586622
104677744946777450CT33GENIChomozygous116586624
104677824346778244GA49GENIChomozygous116586626
104677913046779131CT22GENIChomozygous116586628
104678004146780042TG28GENIChomozygous116586630
104678208146782082AC55GENIChomozygous116586632
104678263746782638GA47GENIChomozygous116586634
104678328946783290GA32GENICpossibly homozygous116586636
104678354046783541GA45GENIChomozygous116586638