chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148692226686922267GA13GENIChomozygous113607325
148692238186922382CA7GENIChomozygous113607326
148692244386922444AG14GENIChomozygous113607327
148692288486922885CA16GENIChomozygous113607328
148692291786922918TC12GENIChomozygous113607329
148692322386923224GA22GENIChomozygous113607330
148692347586923476CG25GENIChomozygous113607331
148692379286923793CT12GENICheterozygous113607332
148692381286923813AG9GENIChomozygous113607333
148692464686924647GA19GENIChomozygous113607334
148692647586926476CT22GENIChomozygous113607335
148693177886931779GT21GENIChomozygous113607336
148693212486932125CT31GENIChomozygous113607337
148693453486934535CT21GENIChomozygous113607338
148693471586934716TC20GENIChomozygous113607339
148693657986936580AG12GENIChomozygous113607340
148693673286936733GA11GENIChomozygous113607341
148693679686936797TC22GENIChomozygous113607342
148693691586936916AG11GENIChomozygous125971879
148693692486936925AC17GENIChomozygous113607343
148693769686937697CT18GENIChomozygous113607344
148693777986937780GC22GENIChomozygous113607345
148693784686937847GA14GENIChomozygous113607346
148693818586938186GA22GENIChomozygous113607347
148693822586938226TC19GENIChomozygous113607348
148693841586938416AG20GENIChomozygous113607349
148693843986938440GA20GENIChomozygous113607350
148693959786939598CA27GENIChomozygous113607351
148693965786939658CG3GENICheterozygous125971880