chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204592832145928322GC19GENIChomozygous109440545
204595487745954878CT60GENICheterozygous119823392
204595497145954972CT62GENICheterozygous119823393
204595740545957406GT39GENICheterozygous119798056
204595740845957409GA40GENICheterozygous119798058
204595753345957534GA31GENICheterozygous119798062
204596713245967133CG19GENIChomozygous109212023
204596713845967139CA19GENIChomozygous109212027
204596714245967143CG19GENIChomozygous109212029
204596714545967146CG19GENIChomozygous109212031
204596714845967149CG19GENIChomozygous109212033
204596727145967272TA24GENICpossibly homozygous109212035
204597066245970663TA32GENIChomozygous109212037
204597354945973550TA28GENIChomozygous109212043
204597364645973647AC30GENIChomozygous109212045
204597367345973674GC34GENIChomozygous109212047
204597824145978242TG30GENIChomozygous109212051
204597843645978437CG44GENIChomozygous119798070
204597852245978523TA19GENIChomozygous119798072
204597856245978563AC24GENIChomozygous119798074
204597878345978784AG19GENIChomozygous119798076
204599287445992875GC11GENIChomozygous119798096
204599287845992879TC10GENIChomozygous119798098
204599288745992888TC14GENIChomozygous119798100
204599289045992891TC14GENIChomozygous119798102
204600474646004747CG20GENICheterozygous119798104
204600519046005191GT45GENICheterozygous119798108
204597062745970628GA29GENIChomozygous109276379
204597815845978159TA47GENIChomozygous109460386
204601689046016891TC19GENICheterozygous119878084
204601729046017291GA59GENICheterozygous119798110
204601786546017866GT6GENIChomozygous119798112
204603741846037419AG4GENIChomozygous119798114
204604026946040270CT42GENICheterozygous119798116
204604027746040278TC42GENICheterozygous119798118
204604028546040286TC44GENICheterozygous119798120
204604032946040330CT60GENICheterozygous119873187
204604037346040374CT64GENICheterozygous119823480