chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2165602862165602863GC18GENIChomozygous110113166
2165607067165607068GA17GENIChomozygous110113167
2165612897165612898AG23GENIChomozygous110113168
2165613554165613555GA13GENIChomozygous110113169
2165613753165613754GA8GENIChomozygous110113170
2165617548165617549AG6GENIChomozygous110113172
2165617598165617599AC8GENIChomozygous110113173
2165618002165618003GT16GENIChomozygous110113174
2165618713165618714GA9GENIChomozygous110113175
2165618927165618928AG17GENIChomozygous110113176
2165618992165618993AG27GENIChomozygous110113177
2165619315165619316TC12GENIChomozygous110113178
2165619724165619725GA19GENIChomozygous110113179
2165620175165620176CT17GENIChomozygous110113181
2165620590165620591TC19GENIChomozygous110113182
2165620767165620768CT20GENIChomozygous110113183
2165621125165621126TC21GENIChomozygous110113184
2165621220165621221TG21GENIChomozygous110113185
2165621566165621567GA12GENIChomozygous110113186
2165621675165621676AG11GENIChomozygous110113187
2165622035165622036TG14GENIChomozygous110113188
2165624356165624357TC24GENIChomozygous110113189
2165624408165624409AG23GENIChomozygous110113190
2165625059165625060TC15GENIChomozygous110113191
2165625863165625864AT8GENIChomozygous120128290
2165626518165626519AG7GENIChomozygous110113192
2165627110165627111TC12GENIChomozygous110113193