chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108918114889181149TG40GENIChomozygous116675224
108918127389181274CT46GENIChomozygous116902220
108918280089182806GAGGGA41GENIChomozygous131902678
108918523189185239ACACACAA40GENICheterozygous131902679
108918354689183547TC37GENICpossibly homozygous116819612
108918424389184244AG66GENIChomozygous116819614
108918608889186089CG38GENIChomozygous116902222
108918679889186799CT53GENIChomozygous116819616
108918852889188528TG43GENIChomozygous131902680
108918859989188600C28GENIChomozygous128843652
108918895989188960TC57GENIChomozygous116819618
108918951289189513CT46GENIChomozygous116902224
108919393189193932CT39GENIChomozygous116902226
108919459389194594TA41GENIChomozygous116819628
108919509389195093A25GENIChomozygous128843653
108919512889195128T25GENICpossibly homozygous128843654
108919519289195193C14GENIChomozygous131902681
108919520889195209A13GENIChomozygous128843655
108919524889195249C11GENIChomozygous128843656
108919525489195255C12GENIChomozygous128843657
108919569489195695TC44GENIChomozygous116819632
108919683089196831AG45GENIChomozygous116819634
108919513089195131CA22GENIChomozygous117068438