chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101288604101288605TG14GENIChomozygous116983364
10101290387101290388G16GENIChomozygous128853916
10101290392101290392C15GENIChomozygous128853917
10101290584101290585CA9GENICpossibly homozygous131712661
10101291337101291338GT19GENIChomozygous116983366
10101292609101292617AGAAAGAG13GENIChomozygous134374310
10101292743101292743AT14GENIChomozygous131097671
10101293093101293094T16GENIChomozygous132694551
10101293612101293613TC9GENIChomozygous116957901