chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113610218336102184GA11GENICheterozygous50731871
113610269736102698TC24GENICpossibly homozygous51400986
113610508636105087AT13GENIChomozygous51400988
113610525336105254TC13GENIChomozygous50731873
113610597436105975GA16GENICheterozygous51400990
113610621136106212AG22GENICpossibly homozygous51001115
113610814636108147AG22GENIChomozygous50731874
113610852236108523CT34GENICpossibly homozygous51400992