chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84971137349711374AG16GENIChomozygous976224809
84971144049711441GA15GENIChomozygous976224810
84971204949712050CG14GENIChomozygous976224811
84971205349712054AC14GENIChomozygous976224812
84971205549712056CA14GENIChomozygous976224813
84971248049712481GT17GENIChomozygous976224814
84971251249712513GA23GENIChomozygous976224815
84971276549712766TC25GENIChomozygous976224816
84971277449712775TC25GENIChomozygous976224817
84971285849712859AG18GENIChomozygous976224818
84971421149714212CT12GENIChomozygous976224819
84971462949714630AC21GENIChomozygous976224820
84971470249714703GA23GENIChomozygous976224821
84971495049714951GA15GENIChomozygous976224822
84971524449715245AG9GENIChomozygous976224823
84971535249715353AG16GENIChomozygous976224824