chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124893276048932761AG18GENICpossibly homozygous50230121
124893354848933549CT19GENICpossibly homozygous50230123
124893518848935190CT--7GENICpossibly homozygous50230129
124893620548936206TG1GENIChomozygous50230131
124893919048939191CT17GENICpossibly homozygous50230137
124893946248939463TG10GENICheterozygous50230140