chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106363891863638919GGAA13GENICpossibly homozygous51672480
106363891863638919GGA13GENICheterozygous51902877
106364533063645331CT29GENIChomozygous51672482
106364655463646555AG23GENIChomozygous51475153
106364659763646598CA35GENIChomozygous51475154
106364660063646601GA35GENIChomozygous51672484
106364769263647697ACAAA-----7GENIChomozygous51672486