chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85097971950979720AG16GENIChomozygous138329685
85098013550980136CT12GENIChomozygous138329686
85098101050981010A15GENIChomozygous138244863
85098153950981540GC23GENIChomozygous138329687
85098166350981664TA15GENIChomozygous138329688
85098186050981861TC18GENIChomozygous138329689
85098326650983267AG9GENIChomozygous138329690
85098386950983870CT6GENIChomozygous138329691
85098441350984414TC15GENIChomozygous138329692
85098925250989253AC10GENIChomozygous138329693
85099147350991474GA19GENIChomozygous138329694
85099226650992267C17GENIChomozygous138244864
85099226750992268CT17GENIChomozygous138329695
85099243950992440CG19GENIChomozygous138329696
85099358050993581TA19GENIChomozygous138329697
85099622150996222CT10GENIChomozygous138329698
85099782450997825AT22GENIChomozygous138329699
85099851950998520GA13GENIChomozygous138329700
85099893150998931TCC14GENIChomozygous138244865
85099966650999667GA20GENIChomozygous138329701
85100103351001033TG11GENIChomozygous138244866
85100107751001077TG10GENIChomozygous138244867
85099625150996252CT13GENIChomozygous154518244
85099625150996252C13GENICheterozygous403237543
85100259051002591C11GENIChomozygous403237544
85100259051002591CA11GENICheterozygous403237545