chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118386883883868839TC22GENICpossibly homozygous51027099
118386930483869305TTCA18GENICpossibly homozygous51295689
118386937783869378TG19GENIChomozygous51418760
118387052683870527AG29GENIChomozygous51027118
118387070183870702TC23GENIChomozygous51027120
118387072383870724AG30GENIChomozygous51596972
118387256883872569AG22GENIChomozygous51027139
118387324283873243TG14GENIChomozygous51596974
118387330483873305AAT14GENIChomozygous51596976
118387331783873318TG20INTERGENIChomozygous51596978