chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91712103817121039TC22INTERGENIChomozygous51775530
91712106017121061GGA15INTERGENIChomozygous51775532
91712122217121223TC29INTERGENIChomozygous51775534
91712154517121546AG20INTERGENIChomozygous51775536
91712169517121696CT32INTERGENIChomozygous51775538
91712173217121733GA38INTERGENIChomozygous51775540
91712183217121834AA--29INTERGENIChomozygous51775542
91712278517122786GA35INTERGENIChomozygous51775544
91712446517124466AC22INTERGENICpossibly homozygous51775546
91712451917124520CCCTCCCTCTCT2INTERGENIChomozygous52900439
91712456217124563CCTG6INTERGENICheterozygous52900441
91712456317124565TG--6INTERGENICheterozygous52900443