chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141626900016269001TC22GENICpossibly homozygous113357775
141626909816269099GA30GENIChomozygous113357777
141627080816270809CA25GENIChomozygous113808682
141627182816271829GA26GENICpossibly homozygous113808684
141627358016273581TC30GENIChomozygous113357793
141627385616273857TC19GENIChomozygous113808686
141627426516274266CT24GENIChomozygous113357795
141627451016274511GA29GENIChomozygous113808688
141627598916275990TC14GENIChomozygous113357805
141627603416276035CT13GENIChomozygous113576648