chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1217040705217040706GA25GENIChomozygous109193698
1217048347217048348AG15GENIChomozygous109193702
1217048900217048901TC25GENIChomozygous108992538
1217049404217049405GA16GENIChomozygous108992543
1217049496217049497TA12GENIChomozygous108992544
1217050037217050038GT13GENIChomozygous108992545
1217050783217050784GT22GENIChomozygous109193704
1217051154217051155AG16GENIChomozygous108992547
1217052345217052346AG21GENIChomozygous108992550
1217053571217053572AG27GENIChomozygous108992551
1217054347217054348GT37GENICpossibly homozygous109193708
1217055064217055065CT24GENIChomozygous109193710
1217055400217055401TC31GENIChomozygous109193712
1217055583217055584AT33GENIChomozygous108992554
1217056931217056932CT21GENIChomozygous108992555
1217060120217060121AT13GENIChomozygous108992558
1217061955217061956AG13GENIChomozygous109193714
1217062350217062351CA24GENIChomozygous108992560
1217063110217063111AC23GENIChomozygous108992561
1217065247217065248GA24GENIChomozygous109193717
1217066288217066289TC33GENIChomozygous108992564