chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4159626317159626318AT29GENICpossibly homozygous119588391
4159626847159626848AG29GENIChomozygous119588392
4159628078159628079CG21GENIChomozygous119588393
4159628333159628334GA31GENIChomozygous119588394