chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57611156776111568AC54GENIChomozygous118843578
57611156876111569TA53GENIChomozygous118843579
57611288976112890GA68GENIChomozygous113869363
57611424076114241CG6GENICheterozygous113869365
57611424576114247AG7GENICpossibly homozygous128199846
57611553176115531G50GENIChomozygous128199847
57611553376115534TC50GENIChomozygous118843580
57611553376115533G51GENIChomozygous128199848
57611556576115566GA53GENIChomozygous113869367
57611582376115823AAAT35GENIChomozygous128199849
57611783776117838CT45GENIChomozygous113869369
57611958176119582GA36GENIChomozygous113869373
57612224576122246AC52GENIChomozygous113869375
57612248376122484AT53GENIChomozygous113869377
57612250576122506AG54GENIChomozygous113869379
57612250676122507TC54GENIChomozygous113869381
57612252276122523AT50GENIChomozygous113869383
57612285876122859AG54GENIChomozygous113869385
57612300276123003GA54GENIChomozygous113869387
57612388476123885AG40GENIChomozygous113869389
57612430176124302T41GENIChomozygous128199850
57612526576125266GA50GENIChomozygous113869391
57612538076125381TC34GENIChomozygous113869393
57612576776125768CA38GENIChomozygous113869397
57612686676126872ATAGAC21GENICpossibly homozygous128199851
57612688176126882TC17GENIChomozygous118854213
57612688476126884AT16GENIChomozygous128199852
57612784876127849CT44GENIChomozygous113869401
57612787976127880GT43GENIChomozygous113869403
57612789976127900AG46GENIChomozygous113869405
57612794076127941GA47GENIChomozygous113869407
57612808476128085CT50GENIChomozygous113869409
57612813776128138GA28GENIChomozygous113869411
57612817176128172AG27GENIChomozygous113869413
57612838176128382CT37GENIChomozygous113869415
57612850976128510CT37GENIChomozygous113869417
57612866876128669GA35GENIChomozygous113869419
57612899776128998CT44GENIChomozygous113869421