chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184055562740555628CT22GENIChomozygous110329405
184055835940558360AG18GENIChomozygous110329407
184055898140558981G10GENIChomozygous129532237
184055904440559044A17GENIChomozygous129532238
184055977840559779CT24GENIChomozygous110329411
184055984740559848TC20GENIChomozygous110329413
184056006040560061GA16GENIChomozygous110329415
184056029840560299TA24GENICpossibly homozygous110329417
184056204240562043TC19GENIChomozygous110329419
184056222740562228TA16GENIChomozygous110329421
184056251040562511AT16GENIChomozygous110329423
184056426240564263GA19GENIChomozygous110329425
184056468340564684AG20GENIChomozygous110329427
184056622140566221ATTG17GENIChomozygous129532239
184056646940566470CT19GENIChomozygous110329429
184056683040566831A16GENIChomozygous129532240
184056812640568127CA8GENIChomozygous110329437
184056648740566488GC18GENIChomozygous110329431
184056718840567189GA12GENIChomozygous110329433
184056768240567683CT16GENIChomozygous110329435
184056083140560832GC17GENICheterozygous129571307
184056083240560833GT17GENICheterozygous129571308
184056908040569080AG11GENIChomozygous129532241
184056966440569664AAGATCGCTGGGCAGGAACACATTAAGTC12GENIChomozygous129532242
184057042640570427GA12GENIChomozygous110329439
184057042940570430GA12GENIChomozygous110329441
184057045140570452CT14GENIChomozygous110329443
184057045440570455CA15GENIChomozygous110329445
184057049540570496CT15GENIChomozygous110329447
184057093940570939TA11GENIChomozygous129532243
184057124040571241TC9GENIChomozygous110329449
184057155040571552TA6GENIChomozygous129532244
184057155440571555GT6GENIChomozygous110329451
184057158940571590C7GENIChomozygous129532245
184057221140572212AG8GENIChomozygous110329453
184057234240572343T5GENIChomozygous129532246
184057251040572511T7GENIChomozygous129532247
184057253540572536AG5GENIChomozygous110329455
184057155940571560CA6GENIChomozygous110684245