chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123809583538095836AC15GENICpossibly homozygous950698598
123810441738104418AT10GENIChomozygous950698599
123811057838110579AG11GENIChomozygous950698600
123811271138112712GA29GENICpossibly homozygous950698601