chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87664071776640718TC8GENIChomozygous53128056
87664332376643324TA11GENIChomozygous53128057
87664516276645163GC19GENIChomozygous53128059
87664539176645392TC19GENICpossibly homozygous53128060
87664560776645608TC12GENIChomozygous53128061
87664638876646389AAT8GENIChomozygous52677306
87664655976646560GT10GENIChomozygous53128063
87664659476646595TTAC7GENIChomozygous53128064
87665061476650615GA16GENIChomozygous53128065
87665080476650805GA15GENICpossibly homozygous53128066
87665222076652221CT23GENICpossibly homozygous53128067
87665244276652443TA19GENICheterozygous53128068
87665279176652792GA19GENIChomozygous53128069