chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109904042109904042G15GENIChomozygous128860841
10109904073109904073G15GENIChomozygous128860842
10109904099109904100G12GENIChomozygous128860843
10109904106109904106G13GENIChomozygous128860844
10109904119109904119G14GENIChomozygous128860845
10109904184109904185C17GENIChomozygous128860846
10109904235109904235C15GENIChomozygous128860847
10109904237109904238A15GENIChomozygous128860848
10109904244109904244C15GENIChomozygous128860849
10109904251109904251CC14GENIChomozygous128860850
10109904290109904291A12GENIChomozygous128860851
10109905640109905641AG14GENIChomozygous116719306
10109904104109904105GC13GENIChomozygous116843120