chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123663857636638577CT21GENIChomozygous115318671
123663899336638994CA30GENIChomozygous115318673
123663912936639130T19GENICpossibly homozygous128985372
123663942136639421A25GENIChomozygous128985373
123663948836639489T30GENIChomozygous128985374
123663952036639521GA27GENIChomozygous115318675
123663963136639633AA24GENIChomozygous128985375
123664019636640196GG25GENIChomozygous128985376
123664019736640198GT25GENIChomozygous115318677
123664020536640205T24GENIChomozygous128985377
123664255036642551TG34GENIChomozygous115440025
123663961136639612AG26GENIChomozygous115380203