chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2211878105211878106CT18GENIChomozygous59378885
2211878602211878603AG18GENICpossibly homozygous59378887
2211878667211878668CT32GENIChomozygous59378889
2211878903211878904CT16GENIChomozygous59378891
2211879193211879194CT8GENICheterozygous59378893
2211879435211879436GC7GENIChomozygous59378897
2211879459211879460A-18GENIChomozygous59378899
2211879511211879512TC13GENICheterozygous59378901