chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124893276048932761AG50GENIChomozygous50230121
124893354848933549CT47GENIChomozygous50230123
124893401848934019CG26GENIChomozygous50230125
124893428348934284CA21GENIChomozygous50230127
124893518848935190CT--41GENIChomozygous50230129
124893620548936206TG37GENICpossibly homozygous50230131
124893642148936422CG21GENICheterozygous50343591
124893642548936426CCGCAGGCAG16GENIChomozygous50230133
124893642548936426CG21GENICheterozygous50343593
124893681948936820GGAAA7GENIChomozygous50230135
124893919048939191CT40GENIChomozygous50230137
124893943948939443AAAA----29GENIChomozygous50230139
124893946248939463TG42GENIChomozygous50230140