chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117754523117754524GA25GENIChomozygous539309561
7117754598117754604TCCTCC------15GENIChomozygous697480780
7117755771117755772AG39GENIChomozygous539309562
7117757970117757971GA28GENIChomozygous539309563
7117758206117758208AG--17GENIChomozygous697480782
7117758394117758395CT18GENIChomozygous540023110
7117758629117758630TTA16GENICpossibly homozygous697480783
7117758787117758788CT20GENIChomozygous539309564
7117758908117758909CT41GENIChomozygous539309565
7117760179117760180TTGTGC16GENIChomozygous697480784
7117760208117760209GA21GENICpossibly homozygous539309566
7117760974117760975GA40GENICpossibly homozygous539309567