chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1195076468195076469TC11GENIChomozygous108475133
1195081077195081078AG15GENIChomozygous120584498
1195081400195081401TC14GENIChomozygous120584500
1195082985195082986GA5GENIChomozygous120584502
1195083102195083103TG9GENIChomozygous120584504
1195083439195083440TC11GENIChomozygous120584506
1195085845195085846AG8GENIChomozygous108978717
1195086688195086689CA17GENIChomozygous108978720
1195087743195087744TG11GENIChomozygous108978724
1195091300195091301CA17GENIChomozygous108978725
1195091531195091532GA18GENIChomozygous120584508
1195091927195091928TC5GENIChomozygous108978727
1195092124195092125TG14GENIChomozygous108978728
1195093268195093269TA18GENIChomozygous120584510
1195094020195094021AG19GENIChomozygous108978730
1195094943195094944AG21GENIChomozygous108978731
1195096097195096098TC4GENIChomozygous108978735