chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77126461671264617AC37GENIChomozygous115710128
77126478171264782AG44GENIChomozygous115710129
77126487071264871GA21GENIChomozygous115710130
77126551471265515GA40GENIChomozygous115710132
77126554571265546AG41GENIChomozygous115710133
77126635371266354TC58GENIChomozygous115710134
77126640471266405CT40GENICpossibly homozygous115710135
77126642071266421CT40GENIChomozygous115710136
77126666971266670TC15GENIChomozygous115710137
77126704371267044TC35GENIChomozygous115710138
77126971671269717CA48GENIChomozygous115710139