chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103965546139655462CT21GENIChomozygous52143364
103965647039656471GC22GENIChomozygous51858004
103966416039664161TG18GENIChomozygous51858049
103966431539664316TC17GENICpossibly homozygous51423906
103966635739666358T-6GENICheterozygous51423908
103966984939669850AG21GENICpossibly homozygous52143368
103967319839673199GA11GENICheterozygous51423915
103967654639676547CT25GENICpossibly homozygous51423922
103967820239678204AA--2GENIChomozygous51423923
103967837039678371TC12GENICpossibly homozygous51858134
103967864439678645T-6GENICheterozygous52044436
103967903439679035GGGA6GENIChomozygous51858152
103967903839679039CT8GENIChomozygous51858155
103967903939679040TTG8GENIChomozygous51858158
103967988939679890AT11GENICheterozygous52143370
103968284439682845CT17GENIChomozygous52143372
103968406039684061AG23GENICpossibly homozygous52143374
103968692739686928C-16GENIChomozygous52143376
103968786339687864T-9GENICheterozygous51985193
103968860539688606TC28GENICpossibly homozygous52143380
103969125839691259GA25GENIChomozygous52143382
103969142039691421CT9GENICpossibly homozygous51423929
103969238639692387T-8GENIChomozygous52143384
103969320939693212TGC---9GENICheterozygous51423931
103969330639693307C-4GENICheterozygous51423933
103969330839693309T-4GENICheterozygous51423934
103969331439693315A-3GENIChomozygous51423935
103969336739693368T-8GENIChomozygous51423936
103969338639693387C-8GENIChomozygous51423937
103969490539694906TG22GENIChomozygous52143386
103969707439697075TC20GENIChomozygous51423939
103969786839697869TC16GENICpossibly homozygous51858231
103970460139704602GA20GENIChomozygous52143394
103970508639705087GA22GENICpossibly homozygous51858252
103970598339705984TC26GENIChomozygous52143396
103970884239708843C-9GENICpossibly homozygous51423943
103970905939709060T-9GENICheterozygous51858279
103970990039709901AG20GENICheterozygous52143398
103971569439715695A-1GENIChomozygous51423949
103971651539716516C-1GENIChomozygous51423950