chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135771298135771299TC33GENICpossibly homozygous56939176
4135772963135772970TGAAGGC-------11GENIChomozygous56939179
4135773034135773035GC8GENIChomozygous56939180
4135773572135773573CCT30GENICpossibly homozygous58659050
4135775241135775243TT--14GENICheterozygous58444218
4135777145135777146GA43GENIChomozygous59635753
4135783100135783101CG20GENIChomozygous56939209