chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X91055909105591CT24GENIChomozygous140609160
X91065179106518CT21GENIChomozygous140609161
X91072489107249GA28GENIChomozygous140609162
X91083439108343T16GENIChomozygous140575607
X91104159110416AG25GENICpossibly homozygous140609163
X91129019112902TC26GENIChomozygous140609164
X91132789113279GA22GENIChomozygous140609165
X91134929113493T30GENIChomozygous140575608
X91137539113754TC20GENIChomozygous140609166