chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3177091749177091750TC38GENIChomozygous774869736
3177094314177094315GA16GENIChomozygous774869737
3177095137177095138CA63GENICpossibly homozygous774869738
3177095365177095366CT35GENIChomozygous774869739
3177095501177095502AT30GENIChomozygous774869740