chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134887368048873681AG30GENIChomozygous66467577
134887725348877254CT20GENIChomozygous66467581
134887781648877817CT14GENIChomozygous66467582
134887859748878598TC20GENIChomozygous66467583
134888090448880905AC25GENIChomozygous66467584
134888241748882418TG28GENIChomozygous66467585
134888243148882432AG30GENICpossibly homozygous66467586
134888243548882436TG30GENIChomozygous66467587
134888251848882519AG23GENIChomozygous66467588
134888252548882526GA22GENIChomozygous66467589
134888283348882834GA24GENIChomozygous66467590
134888294948882950CT14GENIChomozygous66467591
134888322348883224GA21GENIChomozygous66467592
134888359148883592GA15GENIChomozygous66467593
134888398848883989AC23GENIChomozygous66467594
134888403948884040AC27GENIChomozygous66467595
134888180148881802GA3GENICheterozygous65975924
134888410648884107CT14GENIChomozygous66467596
134888410748884108GA15GENIChomozygous66467597
134888445448884455TC18GENIChomozygous66467598
134888470348884704AG17GENIChomozygous66467599
134888493048884931GA18GENIChomozygous66467600
134888497848884979CT21GENIChomozygous66467601
134888499148884992TC20GENIChomozygous66467602
134888564648885647CT17GENIChomozygous66467603