chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73661136636611367TC19GENIChomozygous997375108
73661188936611890CA24GENIChomozygous997375109
73661191036611911AG25GENIChomozygous997375110
73661386536613866CT18GENIChomozygous997375111
73661486636614867TC33GENIChomozygous997375112
73661944836619449AG27GENIChomozygous997375113
73662064036620641GA25GENIChomozygous997375114
73662140836621409AG19GENIChomozygous997375115
73662236036622361GC31GENIChomozygous997375116
73662527536625276TG28GENICpossibly homozygous997375117
73662637036626371GT30GENIChomozygous997375118
73662746036627461TA28GENIChomozygous997375119
73662757536627576GC27GENIChomozygous997375120
73663311936633120GA25GENIChomozygous997375121
73663340936633410CT30GENIChomozygous997375122
73663383236633833TC17GENIChomozygous997375123
73663566936635670GA23GENIChomozygous997375124
73663734636637347TG36GENIChomozygous997375125
73663818436638185CT30GENIChomozygous997375126
73663871236638713AG24GENIChomozygous997375127