chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105735948957359490CT32GENICpossibly homozygous629055752
105735990457359905CT14GENIChomozygous629055753
105735992357359924AG15GENIChomozygous629055754
105736050457360505AG7GENICheterozygous629055755
105736059757360598GGA23GENICpossibly homozygous744877602
105736090657360907TC22GENIChomozygous629055756
105736103257361033CT23GENICpossibly homozygous629055757
105736110157361102GT20GENICpossibly homozygous629055758
105736188857361889CT12GENICheterozygous629055759
105736188957361890TC12GENICheterozygous629055760
105736209757362099AC--19GENIChomozygous744877603