chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104626097104626098T17GENICheterozygous403296834
10104626097104626098TA17GENICpossibly homozygous403296835
10104626099104626100T21GENICheterozygous403296836
10104626099104626100TA21GENICheterozygous403296837