chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5129919037129919038AG17GENIChomozygous55714709
5129920989129920990AAGG5GENICheterozygous56354196
5129921034129921035AG2GENIChomozygous55714719
5129924107129924108GA31GENICpossibly homozygous55714723
5129924837129924840ATC---8GENIChomozygous55714725
5129925351129925352GA14GENICpossibly homozygous55714727
5129926932129926933TC13GENIChomozygous55714733
5129925463129925464CT30GENICpossibly homozygous55714729
5129925890129925891G-21GENIChomozygous55714731