chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157109368157109369CT53GENIChomozygous112905444
4157110290157110291AC33GENIChomozygous112905446
4157111333157111334GA58GENIChomozygous112905448
4157112730157112731CT44GENICpossibly homozygous112905450
4157114712157114713TC37GENIChomozygous112905452
4157117193157117194GA45GENIChomozygous112905454
4157117444157117445GA39GENIChomozygous112905456
4157117576157117577CT48GENICheterozygous112905458
4157120434157120435TG49GENIChomozygous112905460
4157120481157120482AG40GENIChomozygous112905462
4157120498157120499TG36GENIChomozygous112905464
4157120820157120821AT50GENIChomozygous112905466
4157121231157121232AG19GENIChomozygous112905468
4157121600157121601CT36GENIChomozygous112905470
4157121775157121776GT43GENIChomozygous112905472