chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8119215657119215658AG26GENIChomozygous116889208
8119215666119215667AG27GENIChomozygous116889210
8119216514119216515GA26GENICpossibly homozygous117062594
8119217337119217338GA26GENICpossibly homozygous117062598
8119217505119217506AG22GENIChomozygous116676764
8119218816119218817TG12GENIChomozygous116676772
8119219022119219023AG26GENIChomozygous116676778
8119219136119219137AC35GENIChomozygous117062600
8119219142119219143TC33GENIChomozygous116676780
8119219263119219264GA23GENIChomozygous117062602
8119219559119219560GC15GENIChomozygous117062604
8119219759119219760TC27GENICpossibly homozygous117062606
8119220703119220704CT17GENIChomozygous116676802