chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122188564421885645CT23GENICheterozygous126169828
122188568621885687CT15GENICheterozygous126169829
122188588821885889CT13GENICheterozygous126169830
122188592521885926GA20GENICheterozygous126169831
122188600621886007CT25GENICheterozygous126169832
122188607421886075CA19GENICheterozygous126169833
122188626821886269CA27GENICheterozygous126169834
122188777121887772TC12GENICheterozygous126169836
122188792121887922GA23GENICheterozygous126169837
122188817321888174GC22GENICheterozygous126169838
122188851321888514GA23GENICheterozygous126169839
122188907021889071AG26GENICheterozygous126169840
122188920921889210AG15GENICheterozygous126169841
122188935021889351AC22GENICheterozygous126169842
122188947321889474GT15GENICheterozygous126210436
122188958321889584CT23GENICheterozygous126169843
122188960421889605CT25GENICheterozygous126169844
122188973221889733CG18GENICheterozygous126169845
122189066821890669CA4GENIChomozygous126220983
122189067021890671TA4GENIChomozygous126220984
122189067121890672GA4GENIChomozygous126210437
122189068621890687GT19GENICheterozygous126169847
122189072321890724GC29GENICheterozygous126169848
122189484221894843AC8GENICheterozygous126169849
122189909121899092CA4GENIChomozygous118364839
122189911621899117AG14GENIChomozygous118324807
122190740521907406TC11GENIChomozygous126169850
122190849621908497GC6GENIChomozygous126169851
122190922721909228AG8GENIChomozygous126169852
122190953921909540CG15GENIChomozygous126169853
122191018621910187GA7GENIChomozygous126169854
122191018721910188TC7GENIChomozygous126169855
122191023121910232GA18GENICheterozygous126169856
122191640221916403CT17GENICheterozygous118260817
122191740121917402CA16GENICheterozygous126210439
122192253921922540CT5GENICheterozygous126169857
122192321921923220GC21GENIChomozygous115279956
122189888221898883CA4GENIChomozygous126262645