chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171269440412694405TA38GENICpossibly homozygous110960812
171269458712694588CT59GENIChomozygous111398453
171269485412694855GA57GENIChomozygous110960814
171269501912695020GA35GENIChomozygous111169162
171269566412695665CG35GENIChomozygous110960816
171269577812695779GA38GENIChomozygous110960818
171269631112696312CA46GENIChomozygous110960820
171269649112696492TC44GENICpossibly homozygous111169164
171269649512696496TC47GENIChomozygous110960822
171269704712697048AG33GENICpossibly homozygous110960824
171269714212697143AG36GENIChomozygous110960826