chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174983398249833983CG37GENIChomozygous111059918
174984035849840359CT29GENIChomozygous111059919
174984593249845933CT23GENIChomozygous111059920
174985404649854047GA14GENIChomozygous111059921
174985559949855600TA21GENIChomozygous111059922
174985566649855667AG30GENIChomozygous111059923
174985625449856255TG17GENIChomozygous111059924
174987062549870626GA6GENIChomozygous111059925
174987124749871248GA16GENIChomozygous111059926
174987309949873100CA23GENIChomozygous111059927
174987611849876119CT3GENIChomozygous111246384
174988001749880018GT13GENIChomozygous111059928
174988001949880020GT13GENIChomozygous111059929
174988003049880031TC15GENIChomozygous111059930
174988456349884564TG10GENIChomozygous111059932
174988838849888389GC9GENIChomozygous111059933
174989089849890899CT4GENIChomozygous111059934
174989143949891440GT2GENIChomozygous111204254
174989145849891459GA2GENIChomozygous111204255
174989146149891462GA2GENIChomozygous111246389
174989146349891464AT2GENIChomozygous111246391
174989146449891465CT2GENIChomozygous111246393
174989161449891615GC3GENIChomozygous111059935
174989232549892326AG20GENIChomozygous111059936
174989383949893840CT12GENIChomozygous111059937
174989891349898914CT10GENIChomozygous111059938
174989897749898978TA10GENIChomozygous111059939
174989902849899029AC9GENIChomozygous111204260
174989905749899058GA5GENIChomozygous111204261
174989906049899061GT6GENIChomozygous111204262
174989906149899062TA6GENIChomozygous111204263
174989906249899063CT6GENIChomozygous111204264
174989921649899217GC4GENIChomozygous111204266
174990548849905489TG3GENIChomozygous111059942
174991250449912505TC29GENIChomozygous111059943
174991460249914603AT7GENIChomozygous111059946
174991509949915100AG22GENIChomozygous111059947
174992032349920324GC28GENIChomozygous111059948
174992115849921159GA20GENIChomozygous111059949