chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98217197582171976GA51GENICpossibly homozygous52268907
98217217782172178TC48GENIChomozygous52268909
98217244882172449AG61GENIChomozygous52268911
98217247882172479TG65GENIChomozygous52268913
98217286882172872AAAC----38GENIChomozygous52268915
98217402582174027CA--3GENIChomozygous52027745
98217547282175473AC65GENIChomozygous52268917
98217557782175578TC73GENICpossibly homozygous52268919
98217601882176019AG56GENIChomozygous52268921