chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122275083422750835AG32GENIChomozygous115282686
122275298822752989TC30GENIChomozygous115282688
122275313022753131TG33GENIChomozygous115282690
122275353822753539AG20GENIChomozygous115282692
122275357622753577GA22GENIChomozygous115282694
122275465622754657TC38GENIChomozygous115282696
122275468022754681CA30GENIChomozygous115282698
122275512322755124CT16GENIChomozygous115282702
122275520822755209CG29GENIChomozygous115282704
122275547722755478GT19GENICpossibly homozygous115510201
122275585722755858TC44GENIChomozygous115282706
122275589322755894GA33GENIChomozygous115282708
122276171722761718AG26GENIChomozygous115282715
122276305922763060CT37GENIChomozygous115282717
122276318822763189AG36GENIChomozygous115282719
122276385022763851TC32GENIChomozygous115282721
122276392522763926TC23GENIChomozygous115282723
122276401622764017CG31GENIChomozygous115282725
122276419322764194AC24GENIChomozygous115282727
122276420122764202CT23GENIChomozygous115282729
122275984222759843AT22GENIChomozygous115367052