chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101410079101410080TC20GENIChomozygous108900383
1101410337101410338GT15GENICpossibly homozygous108900385
1101412017101412018TC23GENIChomozygous108900386
1101413255101413256CT22GENIChomozygous108900388
1101413333101413334AG13GENIChomozygous108900390