chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2165602862165602863GC72GENICpossibly homozygous110113166
2165607067165607068GA78GENICpossibly homozygous110113167
2165612897165612898AG98GENICheterozygous110113168
2165613554165613555GA57GENIChomozygous110113169
2165613753165613754GA71GENIChomozygous110113170
2165617221165617222AG57GENICheterozygous110113171
2165617548165617549AG95GENIChomozygous110113172
2165617598165617599AC72GENICpossibly homozygous110113173
2165618002165618003GT90GENIChomozygous110113174
2165618713165618714GA63GENIChomozygous110113175
2165618927165618928AG77GENIChomozygous110113176
2165618992165618993AG73GENICpossibly homozygous110113177
2165619315165619316TC67GENIChomozygous110113178
2165619724165619725GA60GENIChomozygous110113179
2165619893165619894GA60GENIChomozygous110113180
2165620175165620176CT67GENIChomozygous110113181
2165620590165620591TC50GENIChomozygous110113182
2165620767165620768CT55GENIChomozygous110113183
2165621125165621126TC59GENIChomozygous110113184
2165621220165621221TG77GENIChomozygous110113185
2165621566165621567GA74GENIChomozygous110113186
2165621675165621676AG93GENIChomozygous110113187
2165622035165622036TG73GENIChomozygous110113188
2165624356165624357TC83GENICpossibly homozygous110113189
2165624408165624409AG73GENIChomozygous110113190
2165625059165625060TC48GENICpossibly homozygous110113191
2165626518165626519AG70GENIChomozygous110113192
2165627110165627111TC62GENIChomozygous110113193
2165627172165627173CG62GENIChomozygous110113194
2165628868165628869TC10GENIChomozygous110113195