chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7126399655126399656CCA40GENIChomozygous54099646
7126399694126399695TC60GENIChomozygous54099647
7126399866126399867AC59GENIChomozygous54099648
7126399945126399946CT60GENIChomozygous54099649
7126400072126400073AG58GENICpossibly homozygous54099650
7126400117126400118GA43GENICpossibly homozygous54099651
7126400472126400473TC63GENIChomozygous54099652
7126400770126400774CTCT----45GENIChomozygous54099653
7126401402126401403AG61GENIChomozygous54099654
7126401814126401815CT69GENICpossibly homozygous54099655
7126402663126402664GA36GENIChomozygous54099656
7126402667126402668CT35GENIChomozygous54099657
7126402706126402707GA38GENIChomozygous54099658
7126402802126402803GA42GENIChomozygous54099659