chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109988140109988141AG19GENIChomozygous116909796
10109988792109988793GC10GENIChomozygous116909797
10109990105109990106CT21GENIChomozygous116909798
10109991161109991162TC13GENIChomozygous116909799
10109991222109991223TC19GENICpossibly homozygous116909800
10109993188109993189GC8GENIChomozygous116719413
10109997813109997814AG21GENIChomozygous116909801
10109999322109999323CT21GENIChomozygous116909802
10110004845110004846G17GENIChomozygous128861027
10109989365109989366AG17GENIChomozygous116961984
10109992748109992749CT21GENIChomozygous118071214