chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134564186945641870GA39GENIChomozygous145802213
134564195445641955GA30GENIChomozygous142367866
134564202445642025TG27GENIChomozygous139286846
134564230745642308GA15GENIChomozygous154798147
134564255145642552TC28GENIChomozygous142367867
134564274345642744GT50GENICpossibly homozygous139286848
134564320645643207CT39GENIChomozygous142367869
134564332445643325TC39GENIChomozygous139286849
134564336045643361CT41GENICpossibly homozygous145802214
134564539245645393GA29GENIChomozygous139286852
134564642145646422GA41GENIChomozygous139286853
134564722745647228AT49GENIChomozygous139286854
134564854045648541GT57GENIChomozygous145802215
134564214845642149A42GENIChomozygous142343740
134564732945647345TGTGTGTGTGTGTGTA24GENIChomozygous145782518