chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123756400437564005CA31GENIChomozygous958962073
123756478437564785TC36GENIChomozygous958962074
123756704537567046TC26GENIChomozygous958962075
123756727637567277AC36GENIChomozygous958962076
123756739737567398TC26GENIChomozygous958962077
123756789837567899CT29GENIChomozygous958962078
123756793937567940AC30GENIChomozygous958962079
123756948137569482CG22GENIChomozygous958962080
123756973237569733GA18GENIChomozygous958962081
123757086937570870GA23GENIChomozygous958962082
123757167337571674AG32GENIChomozygous958962083
123757232737572328GA23GENIChomozygous958962084
123757460937574610CA5GENIChomozygous958962085
123757461037574611TG5GENIChomozygous958962086
123757461937574620AG5GENIChomozygous958962087
123757463337574634CG6GENIChomozygous958962088
123757853837578539GA19GENIChomozygous958962089
123757871537578716CA24GENIChomozygous958962090
123757948237579483TC11GENIChomozygous958962091
123757991637579917GT16GENIChomozygous958962092
123757991737579918AG16GENIChomozygous958962093
123757995837579959CT22GENIChomozygous958962094