chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57611156776111568AC26GENIChomozygous118843578
57611156876111569TA27GENIChomozygous118843579
57611288976112890GA13GENIChomozygous113869363
57611424076114241CG2GENIChomozygous113869365
57611424576114247AG3GENIChomozygous128199846
57611553176115531G22GENIChomozygous128199847
57611553376115534TC22GENIChomozygous118843580
57611553376115533G22GENIChomozygous128199848
57611556576115566GA24GENIChomozygous113869367
57611582376115823AAAT19GENIChomozygous128199849
57611783776117838CT21GENIChomozygous113869369
57611958176119582GA16GENIChomozygous113869373
57612224576122246AC24GENIChomozygous113869375
57612248376122484AT20GENIChomozygous113869377
57612250576122506AG18GENIChomozygous113869379
57612250676122507TC18GENIChomozygous113869381
57612252276122523AT21GENIChomozygous113869383
57612285876122859AG21GENIChomozygous113869385
57612300276123003GA32GENIChomozygous113869387
57612388476123885AG14GENIChomozygous113869389
57612430176124302T18GENIChomozygous128199850
57612526576125266GA26GENIChomozygous113869391
57612538076125381TC17GENIChomozygous113869393
57612576776125768CA21GENIChomozygous113869397
57612686676126872ATAGAC18GENIChomozygous128199851
57612688176126882TC16GENIChomozygous118854213
57612688476126884AT16GENIChomozygous128199852
57612784876127849CT25GENIChomozygous113869401
57612787976127880GT26GENIChomozygous113869403
57612789976127900AG24GENIChomozygous113869405
57612794076127941GA22GENIChomozygous113869407
57612808476128085CT29GENIChomozygous113869409
57612813776128138GA29GENIChomozygous113869411
57612817176128172AG30GENIChomozygous113869413
57612838176128382CT26GENIChomozygous113869415
57612850976128510CT26GENIChomozygous113869417
57612866876128669GA32GENIChomozygous113869419
57612899776128998CT21GENIChomozygous113869421