chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124893276048932761AG35GENIChomozygous50230121
124893354848933549CT24GENICpossibly homozygous50230123
124893401848934019CG21GENIChomozygous50230125
124893428348934284CA28GENIChomozygous50230127
124893518848935190CT--19GENIChomozygous50230129
124893620548936206TG27GENIChomozygous50230131
124893642548936426CCGCAGGCAG11GENIChomozygous50230133
124893681948936820GGAAA9GENICpossibly homozygous50230135
124893919048939191CT13GENIChomozygous50230137
124893943948939443AAAA----11GENIChomozygous50230139
124893946248939463TG19GENICpossibly homozygous50230140