chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123809583538095836AC12GENIChomozygous958962892
123809689938096900TG4GENIChomozygous958962893
123810111338101114GA15GENIChomozygous958962894
123810112338101124GT10GENIChomozygous958962895
123810317538103176AC26GENICpossibly homozygous958962896
123810334438103345AC11GENIChomozygous958962897
123810441738104418AT12GENIChomozygous958962898
123810489138104892GC21GENIChomozygous958962899
123810613938106140CT25GENIChomozygous958962900
123810640838106409GA23GENIChomozygous958962901
123810672638106727AG28GENIChomozygous958962902
123811057838110579AG18GENIChomozygous958962903
123811099638110997GA29GENIChomozygous958962904
123811451638114517AT12GENIChomozygous958962905