chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99813663898136642AGTC----30GENIChomozygous52066290
99813688798136888TC31GENIChomozygous52066293
99813722098137221CT47GENIChomozygous52066296
99813844098138441G-27GENIChomozygous52066298
99813892498138933CCCCTGCCT---------3GENIChomozygous53210699
99813936998139370CT32GENIChomozygous52066302
99813941298139413A-37GENIChomozygous52066304
99814004098140041AG40GENIChomozygous52066307
99814115298141184CTGTGCTGCCCCAGGTCTGAGCCTTAAGCTGG--------------------------------33GENIChomozygous53084883
99814213098142131CT39GENIChomozygous52066309
99814300598143006TC37GENIChomozygous52066312
99814329698143297TC30GENIChomozygous52066314
99814334098143342AC--30GENIChomozygous52066317
99814358398143584AG66GENIChomozygous52066320
99814398098143981CT29GENIChomozygous52066323
99814436298144363TC38GENIChomozygous52066325
99814481298144813AC51GENIChomozygous52066328
99814481498144815GA47GENIChomozygous52066330
99814486098144861AG49GENIChomozygous52066333
99814512098145121GA53GENIChomozygous52066336
99814513998145140CT50GENIChomozygous52066338
99814527998145280GT53GENIChomozygous52066341
99814566798145668GT27GENIChomozygous52066344
99814651998146520AT52GENIChomozygous52066346
99814663098146631AG38GENIChomozygous52066349
99814733198147340TTCTTTTTT---------17GENICpossibly homozygous52066351
99814744898147449AT32GENIChomozygous52066354
99814856598148566TC39GENIChomozygous52066357
99814915098149151GA51GENIChomozygous52066359
99814930498149305GA34GENIChomozygous52066362
99815079098150791GA46GENIChomozygous52066365
99815228298152283GA32GENICpossibly homozygous52066367
99815268998152690GA30GENIChomozygous52066370
99815270498152705TC36GENIChomozygous52066372
99815304798153048AG33GENIChomozygous52066375
99815330298153303AG53GENIChomozygous52066377
99815465098154651CT54GENIChomozygous52066380
99815477398154774GA51GENIChomozygous52066382
99815479098154791TC49GENIChomozygous52066385
99815486898154869AG51GENIChomozygous52066388
99815491198154912GA51GENIChomozygous52066391
99815549098155491AG50GENIChomozygous52066397
99815552698155527GA53GENICpossibly homozygous52066399
99815590698155907TC28GENIChomozygous52066402
99815607398156074GA45GENIChomozygous52066404
99815620398156204AG49GENIChomozygous52066407
99815628498156285CT29GENIChomozygous52066410
99815641498156415TC40GENIChomozygous52066413
99815653198156532GA35GENICpossibly homozygous52066415
99815658398156584TC36GENIChomozygous52066418
99815680198156802AG23GENIChomozygous52066420
99815693898156939GA26GENIChomozygous52066423
99815717798157178TC32GENIChomozygous52066426
99815778098157781CT28GENIChomozygous52066429
99815915598159156GA33GENIChomozygous52066431
99816039398160409TGTTTGTTTGTTTGTT----------------27GENICpossibly homozygous53210702
99816068298160683GC47GENIChomozygous52066436
99816082098160821TC46GENIChomozygous52066439
99816099098160991GA31GENIChomozygous52066441
99816104798161048CT32GENIChomozygous52066444
99816106898161069CCAG33GENIChomozygous52066447
99816113198161132TTGG30GENIChomozygous52066450
99816134498161345TG44GENIChomozygous52066452
99815780698157807TTAGCACAGCACAGCAC9GENIChomozygous53238605
99816038998160409TGTTTGTTTGTTTGTTTGTT--------------------27GENICheterozygous53238606