chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97179701771797018AG9GENIChomozygous117738812
97179701971797020TG9GENIChomozygous117738814
97179745471797455CT14GENIChomozygous117876550
97179795371797954AG5GENICheterozygous126627801