chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85097971950979720AG28GENIChomozygous138329685
85098013550980136CT22GENIChomozygous138329686
85098101050981010A22GENIChomozygous138244863
85098153950981540GC18GENIChomozygous138329687
85098166350981664TA30GENIChomozygous138329688
85098186050981861TC20GENIChomozygous138329689
85098326650983267AG13GENIChomozygous138329690
85098386950983870CT10GENIChomozygous138329691
85098441350984414TC13GENIChomozygous138329692
85098925250989253AC25GENIChomozygous138329693
85099147350991474GA15GENIChomozygous138329694
85099226650992267C16GENIChomozygous138244864
85099226750992268CT16GENIChomozygous138329695
85099243950992440CG21GENIChomozygous138329696
85099358050993581TA18GENIChomozygous138329697
85099622150996222CT15GENIChomozygous138329698
85099782450997825AT24GENIChomozygous138329699
85099851950998520GA17GENIChomozygous138329700
85099893150998931TCC15GENIChomozygous138244865
85099966650999667GA21GENIChomozygous138329701
85100103351001033TG11GENIChomozygous138244866
85100107751001077TG11GENIChomozygous138244867
85098198750981987CACACACG19GENICheterozygous142023735