chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176691508766915088CT28GENIChomozygous47170107
176691543266915433TC28GENICpossibly homozygous47170108
176691555466915555AG33GENIChomozygous47170109
176691566666915667A-35GENIChomozygous47170110
176691634566916346TC29GENIChomozygous47170111
176691663866916639TC49GENIChomozygous47170112
176691667466916675CG52GENIChomozygous47170113
176691689466916895CT36GENICpossibly homozygous47170114