chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118439823184398232TA27GENICpossibly homozygous799897881
118439952184399522CA39GENIChomozygous799897882
118439955184399552TC31GENIChomozygous799897883
118439955584399556TC30GENIChomozygous799897884
118439962184399622GT19GENIChomozygous799897885
118439963784399638AT24GENIChomozygous799897886
118439964884399649CT27GENIChomozygous799897887
118439989684399897GC36GENICheterozygous799897888
118439990084399901GC37GENICpossibly homozygous799897889
118441673384416734GT58GENICheterozygous799897890
118441674184416742CA57GENICheterozygous799897891
118441675984416760CT52GENICheterozygous799897892
118441980584419806CT33GENICheterozygous799897893
118442166684421667CT66GENICheterozygous799897894
118442166984421670TA66GENICheterozygous799897895
118442174384421744CT49GENICheterozygous799897896
118444776084447761AT30GENICpossibly homozygous799897897
118444778784447788AT28GENIChomozygous799897898
118444778984447790AG27GENICpossibly homozygous799897899
118444784684447847GT16GENIChomozygous799897900
118444787284447873GA14GENIChomozygous799897901
118444791284447913GA20GENIChomozygous799897902
118444798884447989CT22GENIChomozygous799897903
118444799684447997CT14GENIChomozygous799897904
118445008884450089TG10GENIChomozygous799897905
118445029984450300GT35GENIChomozygous799897906
118445039184450392CG18GENIChomozygous799897907
118446038084460381CT13GENICheterozygous799897908
118446038284460383CT11GENICheterozygous799897909