chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106676531366765314TC12GENIChomozygous51908967
106676533166765332GA16GENIChomozygous51908969
106676932166769322CT8GENIChomozygous51480192
106676981566769816G-9GENIChomozygous51480193
106677238066772384GTGT----2GENICheterozygous52320413
106678643366786435CT--14GENIChomozygous51480208
106678776366787764GA19GENIChomozygous51908985
106678915066789151CT18GENICheterozygous51908987
106679065566790656TC10GENIChomozygous51480210
106679230666792307CT18GENIChomozygous51908989
106679264866792649A-6GENIChomozygous51480212
106679440166794402TTC9GENICheterozygous52320415
106679779466797795TTC8GENIChomozygous51480216
106679884166798842GA22GENICheterozygous51908993
106680074766800748TTGA6GENICheterozygous51908997
106680110466801105TC12GENIChomozygous51908999
106680549366805494AT18GENIChomozygous51480221
106680594766805948TG17GENICpossibly homozygous51480222
106680748966807490CT30GENICpossibly homozygous51909001