chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171405401514054016AT38GENICpossibly homozygous110965653
171405452714054528AG43GENIChomozygous110965655
171405452814054529GA43GENIChomozygous110965657
171405522714055228GA23GENIChomozygous110965659
171405548714055488AT27GENIChomozygous110965661
171405557214055573AG25GENIChomozygous110965663
171405564314055644AG32GENIChomozygous110965665
171405579914055800CA29GENICpossibly homozygous110965667
171405637414056375CT17GENICpossibly homozygous110965669
171405760614057607CT22GENIChomozygous110965671
171405788314057884TG24GENIChomozygous110965673
171405802814058029AT18GENICpossibly homozygous110965675
171405804014058041CT19GENICpossibly homozygous110965677
171405818414058185GA33GENIChomozygous110965679