chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171057900510579006CA33INTERGENIChomozygous64274634
171057900810579009CA32INTERGENICpossibly homozygous64274636
171058453810584539TG18INTERGENIChomozygous64274638
171058459410584595AT20INTERGENIChomozygous64274640
171058464010584641GT31INTERGENIChomozygous64274642
171058465510584656GT35INTERGENIChomozygous64274644
171058469210584693GT34INTERGENIChomozygous64274646
171058472110584722GT31INTERGENIChomozygous64274648
171058475210584753AG27INTERGENIChomozygous64274650
171058481610584817AG26INTERGENIChomozygous64274652
171058495810584959GT37INTERGENIChomozygous64274654
171058496610584967TG34INTERGENIChomozygous64274656
171058499910585000AG28INTERGENIChomozygous64274658
171059954610599547TC30INTERGENICheterozygous64274660