chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71194709411947095AT19GENICpossibly homozygous53789773
71194747711947478CCAG10GENIChomozygous53789774
71194760911947610GA5GENICheterozygous53789775
71194795411947955CT15GENICpossibly homozygous53789776
71194841811948419TC19GENIChomozygous53789777
71194937211949373AG20GENICpossibly homozygous53789778
71194960911949610AG24GENIChomozygous53789779
71194968511949686CG22GENIChomozygous53789780
71194996211949963AG19GENICheterozygous53789781
71195027911950280AG17GENIChomozygous53789782
71195081611950817CT27GENICpossibly homozygous53789783
71195100711951008AG19GENIChomozygous53789784
71195154111951542TC9GENIChomozygous53789785