chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57611156876111569TA28GENIChomozygous118843579
57611288976112890GA35GENIChomozygous113869363
57611553376115534TC19GENIChomozygous118843580
57611783776117838CT24GENIChomozygous113869369
57611925076119251AG26GENIChomozygous113869371
57611958176119582GA14GENIChomozygous113869373
57612224576122246AC33GENIChomozygous113869375
57612248376122484AT20GENIChomozygous113869377
57612250576122506AG20GENIChomozygous113869379
57612250676122507TC21GENIChomozygous113869381
57612252276122523AT25GENIChomozygous113869383
57612285876122859AG16GENIChomozygous113869385
57612300276123003GA20GENIChomozygous113869387
57612388476123885AG24GENIChomozygous113869389
57612526576125266GA24GENIChomozygous113869391
57612538076125381TC19GENIChomozygous113869393
57612576776125768CA17GENIChomozygous113869397
57612784876127849CT19GENIChomozygous113869401
57612787976127880GT19GENIChomozygous113869403
57612789976127900AG18GENIChomozygous113869405
57612794076127941GA17GENIChomozygous113869407
57612808476128085CT27GENIChomozygous113869409
57612813776128138GA22GENIChomozygous113869411
57612817176128172AG18GENIChomozygous113869413
57612838176128382CT18GENIChomozygous113869415
57612850976128510CT15GENIChomozygous113869417
57612866876128669GA12GENIChomozygous113869419
57612899776128998CT16GENIChomozygous113869421