chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5107416185107416186CT23GENICpossibly homozygous113955630
5107416266107416267TG21GENICheterozygous113955631
5107416276107416277TC23GENICheterozygous113955632
5107416524107416525CA5GENIChomozygous114132711