chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122200948622009487CT249GENICheterozygous50113631
122201594922015950TC162GENICheterozygous51063913
122201596222015963AC145GENICheterozygous51063918
122201598922015990CA74GENICheterozygous51092556
122201599922016000CA65GENICheterozygous51092558
122201600022016001TG65GENICheterozygous51092560
122201776422017765AG86GENICheterozygous51141661
122201780222017803TC113GENICheterozygous51063964
122201780822017809CT124GENICheterozygous50113735
122201780922017810AG130GENICheterozygous50113737
122201794722017948AG239GENICheterozygous50369904
122201795722017958GA229GENICheterozygous50113741
122201795822017959CT228GENICheterozygous50287178
122201812622018127GA249GENICheterozygous51063967
122201815322018154GC250GENICheterozygous50113745
122201816022018161AG250GENICheterozygous50113747
122201818022018181TA250GENICheterozygous50113749
122201831722018318T-75GENICheterozygous50113755
122201832822018329CG43GENICheterozygous50113757
122201834622018347AC20GENICheterozygous50113759
122201849022018491GA15GENICheterozygous51092580
122201849422018495CT15GENICheterozygous51147859
122201850322018504CA13GENICheterozygous51147860
122201851022018511CT11GENICheterozygous51147861
122201851322018514GA11GENICheterozygous50113769