chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85097971950979720AG58GENIChomozygous138329685
85098013550980136CT73GENIChomozygous138329686
85098101050981010A55GENICpossibly homozygous138244863
85098153950981540GC58GENIChomozygous138329687
85098166350981664TA58GENIChomozygous138329688
85098186050981861TC47GENIChomozygous138329689
85098326650983267AG52GENIChomozygous138329690
85098386950983870CT21GENIChomozygous138329691
85098441350984414TC38GENIChomozygous138329692
85098925250989253AC52GENIChomozygous138329693
85099147350991474GA61GENIChomozygous138329694
85099226650992267C67GENIChomozygous138244864
85099226750992268CT69GENIChomozygous138329695
85099243950992440CG58GENIChomozygous138329696
85099358050993581TA51GENIChomozygous138329697
85099622150996222CT23GENIChomozygous138329698
85099782450997825AT59GENIChomozygous138329699
85099851950998520GA54GENIChomozygous138329700
85099893150998931TCC52GENICpossibly homozygous138244865
85099966650999667GA51GENIChomozygous138329701
85100103351001033TG35GENIChomozygous138244866
85100107751001077TG32GENIChomozygous138244867
85100259051002591CA35GENICheterozygous403237545
85099625150996252CT39GENICpossibly homozygous154518244
85099625150996252C39GENICheterozygous403237543
85100259051002591C35GENICpossibly homozygous403237544