chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106388773063887731GT15GENIChomozygous116791601
106388876363888764TC32GENIChomozygous116616634
106389273563892736CT24GENIChomozygous116791605
106389432763894328AT13GENIChomozygous116616636
106389589363895894GA28GENIChomozygous116616638
106389862863898629TC19GENIChomozygous116616642
106390665863906659GT23GENIChomozygous116616654
106390666763906668CT20GENIChomozygous116616656
106390699063906991CT8GENIChomozygous116616658
106391248563912486AG25GENIChomozygous116616660
106390081163900812CT27GENICpossibly homozygous116940741