chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1176188507176188508TG20GENIChomozygous971670552
1176188574176188575CA16GENIChomozygous971670553
1176188845176188846CT25GENIChomozygous971670554
1176188972176188973GA19GENICpossibly homozygous971670555
1176192382176192383TC12GENIChomozygous971670556
1176193196176193197AC15GENIChomozygous971670557
1176193840176193841GA15GENIChomozygous971670558