chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122275083422750835AG15GENIChomozygous115282686
122275298822752989TC20GENIChomozygous115282688
122275313022753131TG14GENICpossibly homozygous115282690
122275353822753539AG16GENIChomozygous115282692
122275357622753577GA28GENIChomozygous115282694
122275465622754657TC22GENIChomozygous115282696
122275468022754681CA15GENIChomozygous115282698
122275479622754797TC5GENIChomozygous115282700
122275512322755124CT25GENIChomozygous115282702
122275520822755209CG23GENIChomozygous115282704
122275585722755858TC35GENIChomozygous115282706
122275589322755894GA33GENIChomozygous115282708
122275705522757056GC13GENICheterozygous115282710
122275984222759843AT34GENIChomozygous115367052
122276171722761718AG27GENIChomozygous115282715
122276305922763060CT27GENIChomozygous115282717
122276318822763189AG27GENIChomozygous115282719
122276385022763851TC33GENIChomozygous115282721
122276392522763926TC27GENIChomozygous115282723
122276401622764017CG33GENIChomozygous115282725
122276419322764194AC15GENIChomozygous115282727
122276420122764202CT14GENIChomozygous115282729