chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56262038262620383CT17GENICpossibly homozygous55420019
56262116662621167TG18GENIChomozygous55420021
56262120462621205AT17GENIChomozygous55420023
56262143462621435GT23GENIChomozygous55420025
56262160062621601CT15GENIChomozygous55420027