chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112080993112080994AG45GENIChomozygous57991148
3112083412112083413TG32GENIChomozygous57991151
3112083477112083478AG33GENIChomozygous57991154
3112083581112083582AG71GENIChomozygous57603011
3112083766112083767AT41GENIChomozygous57991157
3112084701112084702CT46GENIChomozygous57991160
3112085179112085180CT49GENICpossibly homozygous57991162
3112085364112085365AG59GENICpossibly homozygous57991165
3112086077112086080AAC---39GENIChomozygous57991171
3112086078112086080AC--39GENIChomozygous57991174