chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122702184122702185CT22GENIChomozygous115861157
7122702649122702650AG16GENIChomozygous118322360
7122702664122702665AT14GENIChomozygous115861163
7122702703122702703A6GENIChomozygous128513534
7122702648122702649C16GENIChomozygous128513531
7122702679122702680T10GENIChomozygous128513532
7122702681122702682T10GENIChomozygous128513533
7122702705122702707CA6GENIChomozygous128513535
7122702722122702723G3GENIChomozygous128513536
7122702725122702726A3GENIChomozygous128513537
7122703155122703158GGC6GENIChomozygous128513538
7122703161122703162A6GENIChomozygous128513539
7122703171122703173CG8GENIChomozygous128513540
7122703199122703199A15GENIChomozygous128513541
7122703202122703202AA16GENIChomozygous128513542
7122703230122703231GA25GENIChomozygous115861165
7122703557122703558CT25GENIChomozygous115861170
7122703782122703783TC14GENICheterozygous132120316
7122709097122709097GGGGA12GENIChomozygous128513545
7122709101122709101GC17GENIChomozygous128513546
7122709102122709102CAGTGGTAGAGCGCTTGCCTAGCAAGCA17GENIChomozygous128513547
7122710110122710111C26GENIChomozygous128513548
7122710164122710165AC35GENIChomozygous115861180
7122710213122710213T28GENIChomozygous128513549
7122710220122710221T27GENICpossibly homozygous128513550
7122710278122710279C36GENIChomozygous128513551
7122710335122710336A39GENIChomozygous128513552
7122710377122710378G35GENIChomozygous128513553
7122710861122710864ATT37GENIChomozygous131024279
7122703300122703301CT43GENIChomozygous116226341
7122703411122703413TC29GENIChomozygous131433962
7122703548122703549GC28GENIChomozygous118418471
7122704035122704036GA47GENIChomozygous118418472
7122709612122709613GT40GENICpossibly homozygous118418473
7122703781122703782TC14GENICpossibly homozygous118512451
7122703824122703825GA19GENIChomozygous118533381