chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99423873494238735TC25GENIChomozygous967447629
99423878194238782TC23GENIChomozygous967447630
99423891794238918GA17GENIChomozygous967447631
99423896394238964AG22GENIChomozygous967447632
99423900194239002CT22GENIChomozygous967447633
99423913494239135GA30GENIChomozygous967447634
99423918894239189TC32GENIChomozygous967447635
99423932694239327GA33GENIChomozygous967447636
99424098994240990CT15GENIChomozygous967447637
99424207294242073GC26GENIChomozygous967447638
99424233294242333AG15GENIChomozygous967447639
99424236494242365AC18GENIChomozygous967447640
99424429794244298GC31GENIChomozygous967447641
99424750794247508GA20GENIChomozygous967447642
99424763094247631AC13GENIChomozygous967447643
99424796994247970AG26GENIChomozygous967447644
99424805794248058AT27GENICpossibly homozygous967447645
99424848494248485CG25GENIChomozygous967447646
99424942394249424TC18GENIChomozygous967447647
99425083194250832CT16GENIChomozygous967447648
99425212494252125AG17GENIChomozygous967447649