chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X15426781542679GA9GENIChomozygous140602279
X15444241544424A10GENIChomozygous140574073
X15450341545035C4GENIChomozygous140574074
X15461561546157GA15GENIChomozygous140602280
X15479561547957CT15GENIChomozygous140602281
X15506531550654GA10GENIChomozygous140602282
X15516251551631AGAGGC5GENIChomozygous140574075
X15530871553088CT15GENIChomozygous140602283
X15536811553684CTC10GENICheterozygous141060595
X15575361557537AC12GENIChomozygous140602284
X15587251558726A4GENICheterozygous140574076
X15604741560477CAC12GENIChomozygous140574077
X15613141561314A9GENIChomozygous140574078
X15621221562123TG12GENIChomozygous140602285
X15626261562627AT12GENIChomozygous140602286
X15641991564200AT9GENIChomozygous140602287
X15661151566115AAAAAACA14GENIChomozygous140574079
X15663641566365AG20GENIChomozygous140602288
X15690961569097AG10GENIChomozygous140602289
X15692241569225T13GENIChomozygous140574080
X15710081571009GT8GENIChomozygous403473553
X15710081571009G8GENICheterozygous403473554
X15711191571120CG9GENIChomozygous140602290
X15713861571387GA13GENIChomozygous140602291
X15721471572148TG13GENIChomozygous140602292
X15721471572148T13GENICheterozygous403473555
X15725061572507CT15GENIChomozygous140602293