chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106620935966209360CT12GENICheterozygous51907776
106621168966211690AG17GENICheterozygous51907782
106621297666212977GA11GENICheterozygous51907784
106621308266213083CCA11GENICheterozygous51479326
106621453966214540AC12GENICheterozygous51907786
106621490766214908TC16GENICheterozygous51479328
106621516366215164CT18GENICheterozygous51907788
106621813366218134AT18GENICheterozygous51479337
106621813466218135TG18GENICheterozygous51479338
106621869966218700TC37GENICheterozygous51479341
106621944766219448TC13GENICheterozygous51479342