chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3137651649137651650AG27GENIChomozygous73078167
3137651922137651923TC17GENIChomozygous73078169
3137652614137652615TA27GENIChomozygous73078171
3137652917137652918CT27GENIChomozygous73078174
3137653007137653008CA25GENICpossibly homozygous73078176
3137653027137653028CT19GENICpossibly homozygous73078179
3137653052137653053TC18GENIChomozygous73078181
3137653185137653186TC16GENIChomozygous73078183
3137653248137653249AG14GENIChomozygous73078186
3137653550137653551AG28GENIChomozygous72500697
3137653599137653600TG24GENIChomozygous73078188
3137653646137653647CT17GENIChomozygous73078191
3137653763137653764TC21GENIChomozygous73078193
3137653874137653875TA21GENIChomozygous73078195
3137653934137653935GA21GENIChomozygous73078198
3137654337137654338TC25GENIChomozygous72500699
3137654389137654390GA17GENIChomozygous73078200
3137654437137654438GT21GENIChomozygous73078203