chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112080993112080994AG30GENICheterozygous57991148
3112083412112083413TG12GENICheterozygous57991151
3112083477112083478AG22GENICpossibly homozygous57991154
3112083581112083582AG20GENIChomozygous57603011
3112083766112083767AT20GENIChomozygous57991157
3112084701112084702CT15GENIChomozygous57991160
3112085179112085180CT14GENICpossibly homozygous57991162
3112085364112085365AG27GENIChomozygous57991165