chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57611288976112890GA19GENIChomozygous113869363
57611556576115566GA25GENIChomozygous113869367
57611783776117838CT22GENIChomozygous113869369
57611925076119251AG26GENICpossibly homozygous113869371
57611958176119582GA13GENIChomozygous113869373
57612224576122246AC15GENIChomozygous113869375
57612248376122484AT19GENIChomozygous113869377
57612252276122523AT16GENIChomozygous113869383
57612285876122859AG21GENIChomozygous113869385
57612300276123003GA11GENIChomozygous113869387
57612388476123885AG18GENIChomozygous113869389
57612526576125266GA8GENIChomozygous113869391
57612538076125381TC14GENIChomozygous113869393
57612576776125768CA12GENIChomozygous113869397
57612784876127849CT26GENIChomozygous113869401
57612787976127880GT23GENIChomozygous113869403
57612789976127900AG17GENIChomozygous113869405
57612794076127941GA15GENIChomozygous113869407
57612808476128085CT21GENIChomozygous113869409
57612813776128138GA16GENIChomozygous113869411
57612817176128172AG21GENIChomozygous113869413
57612826876128269GC5GENIChomozygous126196420
57612838176128382CT15GENIChomozygous113869415
57612850976128510CT12GENIChomozygous113869417
57612866876128669GA21GENIChomozygous113869419
57612899776128998CT8GENIChomozygous113869421
57612672376126724TA6GENICheterozygous126276248