chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109904042109904042G9GENIChomozygous128860841
10109904073109904073G13GENIChomozygous128860842
10109904099109904100G10GENIChomozygous128860843
10109904106109904106G10GENIChomozygous128860844
10109904119109904119G9GENIChomozygous128860845
10109904184109904185C7GENIChomozygous128860846
10109904235109904235C8GENIChomozygous128860847
10109904237109904238A8GENIChomozygous128860848
10109904244109904244C8GENIChomozygous128860849
10109904251109904251CC9GENIChomozygous128860850
10109904290109904291A13GENIChomozygous128860851
10109904104109904105GC10GENIChomozygous116843120