chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2210899669210899671TG17GENICpossibly homozygous127732814
2210901631210901632CT58GENIChomozygous110223813
2210907545210907546GA55GENIChomozygous110223814
2210911281210911282CT49GENIChomozygous110223815
2210913887210913888TC56GENIChomozygous110223816
2210915102210915103CG38GENIChomozygous110223817
2210921970210921971CT53GENIChomozygous110223818
2210924776210924777AG51GENIChomozygous110223819
2210925196210925197TC38GENICpossibly homozygous110223820
2210925229210925230TC45GENIChomozygous110223821
2210926145210926146GA64GENIChomozygous110223822
2210929343210929344AG34GENIChomozygous110223823