chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195050149050501491CT15GENICpossibly homozygous46492182
195050157350501574AT14GENICpossibly homozygous46492184
195050315750503158GC10GENIChomozygous46154314
195050334450503345TC16GENIChomozygous46154317
195050405550504056GA11GENICpossibly homozygous46492186
195050559450505595CT17GENIChomozygous46492188
195050562050505621GGT7GENIChomozygous46154324
195050562550505626GGT6GENIChomozygous46154325
195050597350505974CT14GENICpossibly homozygous46154328
195050623850506239CT19GENICpossibly homozygous46492190
195050675150506752GA16GENIChomozygous46154331
195050807650508077AG15GENICpossibly homozygous46492192