chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X15426781542679GA9GENIChomozygous140602279
X15444241544424A8GENIChomozygous140574073
X15450341545035C9GENIChomozygous140574074
X15461561546157GA11GENIChomozygous140602280
X15479561547957CT13GENIChomozygous140602281
X15506531550654GA12GENIChomozygous140602282
X15516251551631AGAGGC12GENIChomozygous140574075
X15530871553088CT10GENIChomozygous140602283
X15575361557537AC12GENIChomozygous140602284
X15587251558726A9GENIChomozygous140574076
X15604741560477CAC9GENIChomozygous140574077
X15613141561314A10GENIChomozygous140574078
X15621221562123TG7GENIChomozygous140602285
X15626261562627AT18GENIChomozygous140602286
X15641991564200AT17GENIChomozygous140602287
X15661151566115AAAAAACA16GENIChomozygous140574079
X15663641566365AG15GENIChomozygous140602288
X15690961569097AG16GENIChomozygous140602289
X15692241569225T21GENIChomozygous140574080
X15711191571120CG16GENIChomozygous140602290
X15713861571387GA10GENIChomozygous140602291
X15721471572148TG13GENIChomozygous140602292
X15725061572507CT13GENIChomozygous140602293
X15710091571010GT17GENICheterozygous146328346
X15721471572148T13GENICheterozygous403473555
X15710081571009GT17GENICpossibly homozygous403473553
X15710081571009G17GENICheterozygous403473554