chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171642984516429846GA22GENICheterozygous110970168
171643002516430026TC21GENIChomozygous110970170
171643005216430053AT12GENIChomozygous110970172
171643046816430469AG17GENIChomozygous110970174
171643148816431489GT23GENIChomozygous110970176
171643182616431827GT6GENIChomozygous110970178
171643275016432751TC15GENIChomozygous110970180
171643284416432845AG19GENIChomozygous110970182
171643302816433029TG14GENIChomozygous110970184
171643313016433131GA17GENIChomozygous110970186
171643326216433263GA15GENIChomozygous110970188
171643332716433328CG11GENIChomozygous110970190
171643253116432532CA6GENIChomozygous111173257
171643340716433408AT10GENIChomozygous111173259
171643511616435117GA6GENIChomozygous111173263
171643585116435852GA6GENIChomozygous111173265
171643618316436184TG13GENIChomozygous110970194
171643715416437155GA13GENIChomozygous110970196
171643718216437183GA16GENIChomozygous110970198
171643750916437510AG8GENIChomozygous110970200
171643802316438024CT9GENIChomozygous110970202
171643895816438959GA18GENIChomozygous110970204
171643980816439809CT5GENIChomozygous125543454
171644015516440156AT8GENIChomozygous111173267
171644062616440627TG25GENIChomozygous110970206
171644071916440720TG13GENIChomozygous110970208
171644152616441527CG26GENIChomozygous110970210
171644262916442630GT20GENIChomozygous110970212