chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174984035849840359CT17GENIChomozygous111059919
174984593249845933CT16GENIChomozygous111059920
174985404649854047GA15GENIChomozygous111059921
174985559949855600TA12GENIChomozygous111059922
174985566649855667AG29GENIChomozygous111059923
174985625449856255TG19GENIChomozygous111059924
174987062549870626GA9GENIChomozygous111059925
174987124749871248GA17GENIChomozygous111059926
174987309949873100CA18GENIChomozygous111059927
174988003049880031TC11GENIChomozygous111059930
174988159549881596CA6GENIChomozygous111059931
174988838849888389GC16GENIChomozygous111059933
174989089849890899CT17GENIChomozygous111059934
174987617449876175AT14GENICheterozygous125555834
174987618749876188TA10GENICheterozygous125555835
174988018549880186GT15GENIChomozygous125510534
174989232549892326AG28GENIChomozygous111059936
174989383949893840CT11GENIChomozygous111059937
174990469649904697TC18GENIChomozygous111059941
174991250449912505TC19GENIChomozygous111059943
174991267249912673AG17GENIChomozygous111059944
174991267349912674TC17GENICheterozygous111059945
174991509949915100AG7GENIChomozygous111059947
174992032349920324GC18GENIChomozygous111059948
174992115849921159GA24GENIChomozygous111059949