chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115022972750229728TTTTTTC10GENIChomozygous51004567
115022974450229745GT12GENIChomozygous51357364
115023111850231119CT22GENIChomozygous51357368
115023163950231640TC12GENIChomozygous51004570
115023179650231797AG12GENIChomozygous51004571
115023231050232311AG22GENIChomozygous51357372
115023348750233488TA24GENIChomozygous51357374
115023388850233889A-23GENICpossibly homozygous51288550
115023423750234238CT14GENIChomozygous51357378