chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7113896405113896406AC28GENIChomozygous116079383
7113897108113897109GA19GENIChomozygous116079384
7113899251113899252CT19GENIChomozygous116079385
7113899907113899908GA30GENIChomozygous116079386
7113908228113908229GA32GENIChomozygous116079387
7113912043113912044CT27GENIChomozygous116079388
7113912989113912990AG20GENIChomozygous115833195
7113913375113913376GT23GENIChomozygous116079389
7113909587113909588A32GENICpossibly homozygous130562180
7113904795113904795CATTTCAAGAGT30GENIChomozygous128507844
7113903939113903939AGC21GENIChomozygous132866119
7113907587113907588T18GENIChomozygous131433266
7113916061113916062TA28GENIChomozygous116079395
7113922824113922825A25GENIChomozygous128507847
7113924279113924280AG25GENIChomozygous116079396
7113925012113925013G25GENIChomozygous128507850
7113926107113926108GT31GENIChomozygous116079397
7113926108113926109CT31GENIChomozygous116079398
7113930815113930816CT10GENIChomozygous116079399
7113931322113931323AC19GENIChomozygous115833267
7113932216113932217TC16GENIChomozygous115833269
7113932644113932645TG19GENIChomozygous115833271
7113933319113933320AT14GENIChomozygous115833273
7113933463113933464TC21GENIChomozygous115833275
7113935269113935270C27GENIChomozygous128507851
7113936061113936062AG13GENIChomozygous115833277
7113936143113936143TT11GENIChomozygous128507852
7113936173113936174GA10GENIChomozygous116079400
7113936185113936186AC10GENIChomozygous116079401
7113936241113936241C3GENIChomozygous132866121
7113936246113936246C3GENIChomozygous128507853
7113936471113936472AC23GENIChomozygous116079403
7113938020113938020GCGGGTTCC20GENIChomozygous128507855
7113934623113934624CG10GENICheterozygous132990770
7113934630113934634TCTC10GENICheterozygous132984700