chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124893276048932761AG23GENICpossibly homozygous50230121
124893354848933549CT21GENIChomozygous50230123
124893401848934019CG1GENIChomozygous50230125
124893518848935190CT--15GENIChomozygous50230129
124893642548936426CCGCAGGCAG3GENIChomozygous50230133
124893919048939191CT24GENICpossibly homozygous50230137
124893946248939463TG6GENIChomozygous50230140
124893875548938756T-3GENICheterozygous50513668