chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57611156776111568AC53GENIChomozygous118843578
57611156876111569TA54GENIChomozygous118843579
57611288976112890GA53GENIChomozygous113869363
57611424076114241CG24GENICheterozygous113869365
57611553376115534TC66GENIChomozygous118843580
57611553376115533G67GENIChomozygous128199848
57611424576114247AG23GENICheterozygous128199846
57611553176115531G67GENIChomozygous128199847
57611556576115566GA54GENIChomozygous113869367
57611582376115823AAAT35GENICpossibly homozygous128199849
57611783776117838CT45GENIChomozygous113869369
57611958176119582GA29GENIChomozygous113869373
57612224576122246AC66GENICpossibly homozygous113869375
57612248376122484AT49GENIChomozygous113869377
57612250576122506AG57GENIChomozygous113869379
57612250676122507TC57GENIChomozygous113869381
57612252276122523AT58GENIChomozygous113869383
57612285876122859AG47GENIChomozygous113869385
57612300276123003GA52GENIChomozygous113869387
57612388476123885AG41GENIChomozygous113869389
57612430176124302T35GENIChomozygous128199850
57612526576125266GA41GENIChomozygous113869391
57612538076125381TC41GENIChomozygous113869393
57612576776125768CA39GENIChomozygous113869397
57612686676126872ATAGAC40GENIChomozygous128199851
57612688176126882TC42GENIChomozygous118854213
57612688476126884AT40GENIChomozygous128199852
57612784876127849CT30GENIChomozygous113869401
57612787976127880GT35GENIChomozygous113869403
57612789976127900AG43GENIChomozygous113869405
57612794076127941GA39GENIChomozygous113869407
57612808476128085CT52GENIChomozygous113869409
57612813776128138GA45GENIChomozygous113869411
57612817176128172AG47GENIChomozygous113869413
57612838176128382CT44GENIChomozygous113869415
57612850976128510CT60GENIChomozygous113869417
57612866876128669GA44GENIChomozygous113869419
57612899776128998CT54GENIChomozygous113869421