chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2211878105211878106CT21GENIChomozygous59378885
2211878602211878603AG8GENIChomozygous59378887
2211878667211878668CT16GENIChomozygous59378889
2211878903211878904CT16GENICpossibly homozygous59378891
2211879193211879194CT1GENIChomozygous59378893
2211879435211879436GC6GENICheterozygous59378897
2211879459211879460A-15GENICpossibly homozygous59378899
2211879511211879512TC10GENICheterozygous59378901