chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71093970210939703TC12GENIChomozygous115567660
71094018910940190AG6GENIChomozygous115567662
71094043310940434CA13GENIChomozygous115567664
71094056110940562CA18GENICpossibly homozygous115567666
71094105410941055AG9GENIChomozygous115567668
71094107910941080CT10GENIChomozygous115567670
71094148010941481GA6GENIChomozygous115567672
71094159810941599CG8GENICpossibly homozygous115567674
71094196710941968TC8GENIChomozygous115567678