chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X15426781542679GA17GENIChomozygous140602279
X15444241544424A10GENIChomozygous140574073
X15450341545035C13GENIChomozygous140574074
X15461561546157GA28GENIChomozygous140602280
X15479561547957CT20GENIChomozygous140602281
X15506531550654GA14GENIChomozygous140602282
X15516251551631AGAGGC19GENIChomozygous140574075
X15530871553088CT19GENIChomozygous140602283
X15575361557537AC24GENIChomozygous140602284
X15587251558726A26GENICheterozygous140574076
X15604741560477CAC28GENIChomozygous140574077
X15613141561314A24GENIChomozygous140574078
X15621221562123TG10GENIChomozygous140602285
X15626261562627AT16GENIChomozygous140602286
X15641991564200AT11GENIChomozygous140602287
X15661151566115AAAAAACA23GENIChomozygous140574079
X15692241569225T20GENIChomozygous140574080
X15713861571387GA18GENIChomozygous140602291
X15663641566365AG20GENIChomozygous140602288
X15690961569097AG19GENIChomozygous140602289
X15711191571120CG17GENIChomozygous140602290
X15721471572148TG30GENIChomozygous140602292
X15725061572507CT33GENIChomozygous140602293