chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1116153822116153823AG12GENIChomozygous108191067
1116153924116153925CT10GENIChomozygous108191068
1116154294116154295TG6GENIChomozygous108191070
1116156399116156400GT14GENIChomozygous108191071
1116156475116156476GA9GENIChomozygous108191072
1116156538116156539TC13GENIChomozygous108191073
1116157010116157011AT19GENIChomozygous108191074
1116157086116157087CT24GENICpossibly homozygous108191075
1116157434116157435AT24GENIChomozygous108191076
1116157542116157543CT19GENIChomozygous108191077
1116158701116158702GA19GENIChomozygous108191078