chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101805547518055476GA17GENIChomozygous68331182
101805638518056386TC26GENIChomozygous68331184
101805643718056438AC27GENIChomozygous68331186
101805777118057772TC36GENIChomozygous67763985
101805814518058146CT30GENICpossibly homozygous68331188
101805858618058587CT30GENIChomozygous68331190
101805867218058673AG13GENIChomozygous67763997
101805907818059079AC18GENIChomozygous68331192
101805955918059560TC19GENIChomozygous67764019
101806114718061148GA35GENICpossibly homozygous68331194
101806223018062231AG70GENIChomozygous68331196