chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101494879714948797CCTCTT16GENIChomozygous142197048
101494910314949104TG26GENIChomozygous142219179
101494910614949107G26GENIChomozygous142197049
101494966314949663ATT23GENIChomozygous142197050
101494966614949666GAA24GENIChomozygous142197051
101494966814949671TTC25GENIChomozygous142197052
101494967414949676AA24GENIChomozygous142197053
101494968114949682AC23GENIChomozygous142219180
101494968414949685TC21GENIChomozygous142219181
101495070414950705AC23GENIChomozygous142219182
101495115314951154CT21GENIChomozygous142219183
101495367114953672CT15GENIChomozygous142219184
101495656514956565CT14GENIChomozygous142197054
101495183914951840GT8GENIChomozygous154679353
101495183914951840G8GENICheterozygous403277091
101495640014956401GA19GENIChomozygous142219185
101495787714957878GA13GENIChomozygous142219186