chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109708973109708973A45GENICpossibly homozygous134229391
10109710916109710917CT49GENIChomozygous117136843
10109711454109711455AG35GENIChomozygous116719021
10109713667109713668CT58GENIChomozygous117136844
10109716003109716004AC63GENIChomozygous117136845
10109713410109713411CT52GENIChomozygous117145313