chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155278336252783363GT26GENICpossibly homozygous787059586
155278346852783469TG20GENIChomozygous787059587
155278348252783483TG16GENIChomozygous787059588
155278525052785251CT26GENICheterozygous787059589