chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91712103817121039TC26INTERGENIChomozygous51775530
91712106017121061GGA36INTERGENIChomozygous51775532
91712122217121223TC18INTERGENIChomozygous51775534
91712154517121546AG26INTERGENIChomozygous51775536
91712169517121696CT22INTERGENIChomozygous51775538
91712173217121733GA21INTERGENICpossibly homozygous51775540
91712183217121834AA--17INTERGENIChomozygous51775542
91712278517122786GA35INTERGENIChomozygous51775544
91712446517124466AC5INTERGENIChomozygous51775546
91712451917124520CCCTCCCTCTCT4INTERGENIChomozygous52900439
91712456217124563CCTG2INTERGENICheterozygous52900441