chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4118168100118168101TC44GENIChomozygous113153558
4118168515118168519AATG33GENIChomozygous132604493
4118168531118168532AG34GENIChomozygous113153559
4118168547118168548CT26GENIChomozygous113153560
4118170445118170446TG43GENICpossibly homozygous112821598
4118170975118170976TC38GENIChomozygous112821600
4118170995118170996TC41GENIChomozygous113153561
4118171053118171054CT35GENIChomozygous113153562
4118171065118171066GT35GENIChomozygous113153563