chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91521012115210122AG19GENIChomozygous117267449
91521216915212170GA16GENIChomozygous117267450
91521254315212544AT15GENIChomozygous117267451
91521654415216545GA14GENIChomozygous117267452
91521792115217922GT27GENICpossibly homozygous117267453
91522219315222194GA23GENIChomozygous117267454
91522431515224316CA32GENIChomozygous117267455
91522468015224681AG19GENIChomozygous117792121
91522468115224682GT19GENIChomozygous117792123
91522686215226863TC15GENIChomozygous117267456
91523341915233420AG31GENIChomozygous117267458
91523664715236648CA10GENIChomozygous117460773
91523742115237422GA19GENIChomozygous117267459
91523772615237727GT15GENIChomozygous117267460
91523796315237964CA15GENIChomozygous117267461
91524010915240110AG23GENIChomozygous117267462
91524011215240113AC23GENIChomozygous117267463
91524046215240463AG11GENIChomozygous117267464
91524177015241771GA21GENIChomozygous117267465
91524373815243739TC20GENIChomozygous117267466
91524397815243979TA16GENIChomozygous117460781
91524407615244077CT23GENIChomozygous117267467
91524634515246346TA19GENIChomozygous117267468
91524865915248660TC22GENIChomozygous117267469
91524918615249187TA22GENIChomozygous117267470
91524930715249308CT17GENIChomozygous117267471
91525058415250585CT20GENIChomozygous117267472
91525369515253696AT25GENIChomozygous117267473
91525528515255286CG25GENIChomozygous117267474
91525706515257066GA21GENIChomozygous117267481
91525995915259960GA21GENIChomozygous117267482
91526185415261855CT16GENIChomozygous117267483
91526296515262966GC11GENIChomozygous117460796
91526316215263163AG19GENIChomozygous117267484