chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105690987956909880CT13GENICheterozygous51657700
105691182756911828CT19GENICheterozygous52059806
105691406156914062TC10GENIChomozygous51460567
105691502756915028TC12GENIChomozygous51460569
105691574456915745AAT19GENICheterozygous52562472
105691594756915948TTA8GENICheterozygous52562475
105691831556918316AAG11GENIChomozygous51460574
105691871856918719T-10GENICheterozygous52059812
105691929656919297AG10GENIChomozygous51460575
105692135256921353TC9GENIChomozygous52059814
105692487856924879AAC8GENIChomozygous52059820
105692553756925538GA16GENIChomozygous52059822