chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108691389286913893CA111GENICheterozygous51529079
108691391586913916CG107GENICheterozygous51529080
108691391886913919CA113GENICheterozygous51529081
108691392686913927TC119GENICheterozygous51529082
108691393986913940GT120GENICheterozygous51529083
108691394786913948CCA118GENICheterozygous51529084
108692737286927373CT57GENICheterozygous51529122
108692804586928046GT19GENICheterozygous51529123
108692888686928887CT53GENICheterozygous51529125
108692891286928913TC46GENICheterozygous51529126
108692979886929799GC26GENICheterozygous51529128
108693013286930133AG25GENICheterozygous51529129