chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1104023897104023898CT15GENIChomozygous108904422
1104024861104024862CT17GENIChomozygous120888336
1104024905104024906AC19GENIChomozygous108904423
1104025849104025850GA32GENICpossibly homozygous108904424
1104025939104025940AG26GENIChomozygous120888337
1104032336104032337AG5GENIChomozygous120888338
1104032610104032611GA41GENIChomozygous120888339
1104032979104032980CA18GENIChomozygous108904428
1104034839104034840CT23GENIChomozygous120888340
1104035791104035792AG26GENIChomozygous120888341
1104038036104038037AG21GENIChomozygous108904432
1104038038104038039CT21GENIChomozygous120888342
1104038119104038120AC15GENIChomozygous108904433
1104038472104038473AG46GENIChomozygous108904434
1104039103104039104TC42GENIChomozygous120888343
1104040657104040658GA28GENIChomozygous120888344
1104042430104042431AG27GENIChomozygous120888345
1104042772104042773AT25GENIChomozygous120888346
1104043867104043868AT10GENIChomozygous120888347
1104044230104044231TC11GENIChomozygous120888348
1104044651104044652TC34GENIChomozygous120888349
1104047205104047206CA45GENIChomozygous120888350
1104048589104048590CT24GENIChomozygous108904447