chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106605390066053901AAT1GENIChomozygous52382531
106605632166056322TTA5GENICheterozygous51479035
106605703666057037A-2GENICheterozygous52382533
106606284766062848TC22GENICpossibly homozygous51479043
106606541966065420CCTTTT1GENIChomozygous51479049
106606639166066392GC7GENIChomozygous51479050
106606862366068624TG24GENIChomozygous51479055
106606896766068968AAT6GENICheterozygous51479056
106608150866081509CT32GENICpossibly homozygous51907730