chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101502052215020523CT5GENICheterozygous52113038
101502056315020564TC14GENICheterozygous51330849
101502181715021818TC4GENIChomozygous51330853
101502216115022162CG16GENIChomozygous51330854
101502224915022250AG19GENICpossibly homozygous51330855
101502453115024532GA14GENICpossibly homozygous52113040