chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57611288976112890GA64GENIChomozygous113869363
57611424076114241CG104GENICheterozygous113869365
57611556576115566GA31GENIChomozygous113869367
57611783776117838CT63GENIChomozygous113869369
57611925076119251AG49GENIChomozygous113869371
57611958176119582GA39GENIChomozygous113869373
57612224576122246AC56GENIChomozygous113869375
57612248376122484AT47GENIChomozygous113869377
57612250576122506AG35GENIChomozygous113869379
57612250676122507TC34GENIChomozygous113869381
57612252276122523AT31GENIChomozygous113869383
57612285876122859AG49GENIChomozygous113869385
57612300276123003GA49GENIChomozygous113869387
57612388476123885AG46GENIChomozygous113869389
57612526576125266GA50GENIChomozygous113869391
57612538076125381TC39GENIChomozygous113869393
57612576776125768CA37GENIChomozygous113869397
57612697576126976TG35GENICpossibly homozygous113869399
57612784876127849CT61GENIChomozygous113869401
57612787976127880GT66GENICpossibly homozygous113869403
57612789976127900AG63GENIChomozygous113869405
57612794076127941GA46GENIChomozygous113869407
57612808476128085CT44GENIChomozygous113869409
57612813776128138GA36GENIChomozygous113869411
57612817176128172AG42GENIChomozygous113869413
57612838176128382CT40GENIChomozygous113869415
57612850976128510CT52GENIChomozygous113869417
57612866876128669GA34GENIChomozygous113869419
57612899776128998CT34GENIChomozygous113869421