chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7126399655126399656CCA1GENIChomozygous54099646
7126399694126399695TC12GENICpossibly homozygous54099647
7126399866126399867AC5GENIChomozygous54099648
7126399945126399946CT13GENICpossibly homozygous54099649
7126400072126400073AG28GENICpossibly homozygous54099650
7126400117126400118GA21GENICpossibly homozygous54099651
7126400472126400473TC24GENICpossibly homozygous54099652
7126400770126400774CTCT----12GENIChomozygous54099653
7126401402126401403AG12GENICheterozygous54099654
7126401814126401815CT25GENIChomozygous54099655
7126402663126402664GA2GENIChomozygous54099656
7126402667126402668CT2GENIChomozygous54099657
7126402706126402707GA7GENICpossibly homozygous54099658
7126402802126402803GA5GENICheterozygous54099659