chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106388773063887731GT21GENIChomozygous116791601
106388876363888764TC31GENIChomozygous116616634
106389273563892736CT32GENIChomozygous116791605
106389432763894328AT26GENIChomozygous116616636
106389589363895894GA20GENIChomozygous116616638
106389630663896307CT20GENICpossibly homozygous116616640
106389862863898629TC23GENIChomozygous116616642
106390081163900812CT27GENIChomozygous116940741
106390665763906658TG35GENIChomozygous116616652
106390665863906659GT35GENIChomozygous116616654
106390666763906668CT34GENIChomozygous116616656
106390699063906991CT21GENIChomozygous116616658
106391248563912486AG18GENIChomozygous116616660