chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113579659113579660CT17GENIChomozygous117631173
9113579830113579831GC21GENICheterozygous117427220
9113580060113580061GA16GENIChomozygous117631175
9113580355113580356AC16GENICheterozygous117427227
9113580369113580370AC17GENICheterozygous123232926
9113585514113585515GA15GENIChomozygous117631183
9113585908113585909TC12GENIChomozygous117631185
9113585964113585965CA12GENIChomozygous117631187
9113581328113581329C29GENIChomozygous128746397
9113580413113580414TG18GENICheterozygous117831324
9113580430113580431AT19GENICheterozygous117831326
9113588660113588661AT30GENIChomozygous117631189
9113588989113588990GT21GENIChomozygous117631191
9113588994113588995GC22GENIChomozygous117631193
9113591817113591818CT14GENIChomozygous117645427
9113592821113592822TC8GENIChomozygous117427237
9113594294113594295GA24GENIChomozygous117631195
9113594383113594384TC20GENIChomozygous117645430
9113596836113596837TC17GENIChomozygous117645432
9113594928113594943TGCTTTTCTTCTTTG22GENIChomozygous131456378
9113597006113597007A7GENICheterozygous131456379