chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108877114108877115CT16GENICheterozygous579411100
10108877194108877195CT17GENICpossibly homozygous579411101
10108877595108877596TG23GENIChomozygous579411102
10108877657108877658AG20GENICpossibly homozygous579411103
10108877702108877703AT20GENICpossibly homozygous579411104
10108877811108877819GCTTGCCT--------1GENIChomozygous717012951
10108878644108878645TC9GENIChomozygous579411105