chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X15426781542679GA10GENIChomozygous140602279
X15444241544424A11GENIChomozygous140574073
X15450341545035C7GENIChomozygous140574074
X15461561546157GA6GENIChomozygous140602280
X15479561547957CT7GENIChomozygous140602281
X15516251551631AGAGGC4GENIChomozygous140574075
X15536811553684CTC9GENICheterozygous141060595
X15587251558726A8GENICpossibly homozygous140574076
X15604741560477CAC9GENIChomozygous140574077
X15613141561314A5GENIChomozygous140574078
X15621221562123TG10GENIChomozygous140602285
X15506531550654GA13GENIChomozygous140602282
X15530871553088CT14GENIChomozygous140602283
X15575361557537AC7GENIChomozygous140602284
X15626261562627AT10GENIChomozygous140602286
X15641991564200AT15GENIChomozygous140602287
X15661151566115AAAAAACA12GENIChomozygous140574079
X15663641566365AG8GENIChomozygous140602288
X15690961569097AG9GENIChomozygous140602289
X15692241569225T10GENIChomozygous140574080
X15711191571120CG14GENIChomozygous140602290
X15713861571387GA14GENIChomozygous140602291
X15721471572148TG12GENIChomozygous140602292
X15725061572507CT12GENIChomozygous140602293
X15721471572148T12GENICheterozygous403473555
X15710081571009GT10GENIChomozygous403473553
X15710081571009G10GENICheterozygous403473554