chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101410002101410003GT40GENIChomozygous109046578
1101410079101410080TC50GENIChomozygous108900383
1101410337101410338GT48GENIChomozygous108900385
1101410358101410358AA29GENICheterozygous132530330
1101410364101410366AA28GENIChomozygous132530331
1101410376101410379TTC25GENICheterozygous132933099
1101410456101410457T50GENIChomozygous132530332
1101412017101412018TC66GENICpossibly homozygous108900386
1101413255101413256CT65GENIChomozygous108900388
1101413333101413334AG40GENIChomozygous108900390