chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4214460606214460607GC26GENIChomozygous57079780
4214460809214460810GA18GENIChomozygous57079781
4214461097214461098GC20GENICheterozygous57637488
4214461224214461225AG21GENIChomozygous57079783
4214461448214461449CT20GENIChomozygous57637490
4214461451214461452AT19GENICpossibly homozygous57637492
4214461455214461456GC16GENIChomozygous57637494
4214461472214461473TC16GENIChomozygous57079786
4214461381214461382CT20GENICpossibly homozygous57365550