chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143649841143649842GA12GENIChomozygous595537870
5143650275143650276CT10GENICpossibly homozygous595537871
5143650874143650875T-1GENIChomozygous727091878
5143652921143652922CCT1GENIChomozygous727091879
5143653991143653992AG10GENICheterozygous597400788
5143654022143654023CT2GENIChomozygous595537872
5143654168143654169AG8GENIChomozygous595537873
5143654180143654181CG5GENIChomozygous595537874
5143654658143654659AG17GENICpossibly homozygous595537875
5143656319143656320TC25GENIChomozygous595537876
5143657836143657837G-15GENICheterozygous727091880
5143663904143663905AG13GENIChomozygous595537877
5143664036143664037A-7GENIChomozygous727091881
5143664037143664038AT7GENIChomozygous597400789
5143664536143664537AG10GENICheterozygous595537878