chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108877114108877115CT7GENICpossibly homozygous590042055
10108877194108877195CT6GENIChomozygous590042056
10108877595108877596TG11GENIChomozygous590042057
10108877657108877658AG9GENIChomozygous590042058
10108877702108877703AT9GENICheterozygous590042059
10108877811108877819GCTTGCCT--------1GENIChomozygous723355976
10108878644108878645TC7GENIChomozygous590042060