chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188512790188512791GA22GENICpossibly homozygous110169316
2188513887188513888CG32GENIChomozygous120129835
2188513888188513889GC32GENIChomozygous120129836
2188517715188517716CT22GENIChomozygous110169321
2188517754188517755AT25GENIChomozygous110169323
2188518455188518456GA25GENIChomozygous110169325
2188519138188519139CG45GENICpossibly homozygous110169327
2188520309188520310AG29GENIChomozygous110169331