chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X15426781542679GA35GENIChomozygous140602279
X15444241544424A17GENIChomozygous140574073
X15450341545035C32GENIChomozygous140574074
X15461561546157GA33GENIChomozygous140602280
X15479561547957CT25GENIChomozygous140602281
X15506531550654GA25GENIChomozygous140602282
X15516251551631AGAGGC12GENIChomozygous140574075
X15530871553088CT31GENIChomozygous140602283
X15575361557537AC23GENIChomozygous140602284
X15587251558726A19GENICpossibly homozygous140574076
X15604741560477CAC21GENIChomozygous140574077
X15613141561314A29GENIChomozygous140574078
X15621221562123TG13GENIChomozygous140602285
X15626261562627AT39GENIChomozygous140602286
X15641991564200AT26GENIChomozygous140602287
X15661151566115AAAAAACA30GENIChomozygous140574079
X15663641566365AG21GENIChomozygous140602288
X15690961569097AG31GENIChomozygous140602289
X15692241569225T33GENIChomozygous140574080
X15711191571120CG26GENIChomozygous140602290
X15713861571387GA26GENIChomozygous140602291
X15721471572148TG31GENIChomozygous140602292
X15725061572507CT27GENIChomozygous140602293
X15710081571009GT26GENIChomozygous403473553
X15710081571009G26GENICheterozygous403473554
X15721471572148T31GENICheterozygous403473555