chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4226955054226955055T-9GENICpossibly homozygous723893711
4226955162226955163GT13GENIChomozygous589193376
4226956356226956357GGT11GENIChomozygous723893712
4226957610226957611TC17GENIChomozygous589193377
4226959300226959301GGTC6GENIChomozygous723893713
4226959593226959594AC4GENICheterozygous589193378
4226961067226961068GA12GENICpossibly homozygous589193379