chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115389384115389385TC44GENIChomozygous112815428
4115389598115389599TC53GENIChomozygous112815430
4115389864115389865GA60GENIChomozygous119406489
4115390112115390113TC63GENIChomozygous119406490
4115391716115391717CT40GENIChomozygous119406491
4115394660115394661TC49GENIChomozygous112815434
4115395610115395611TA53GENIChomozygous112815436
4115394354115394355GT29GENICpossibly homozygous119625061
4115391970115391970TGATGT50GENIChomozygous128070897
4115394627115394628A43GENIChomozygous128070898
4115395971115395971T23GENIChomozygous128070899
4115396016115396017CA28GENIChomozygous112815438
4115396105115396106TC41GENIChomozygous112815440
4115396201115396202TG47GENIChomozygous112815442
4115397555115397556TA65GENICpossibly homozygous119406492
4115397877115397880GTA53GENIChomozygous128070900
4115399827115399828GT49GENICpossibly homozygous119406493
4115400915115400916GA60GENIChomozygous119406494
4115401003115401004CG59GENIChomozygous119406495
4115401097115401098CT68GENIChomozygous112815452
4115401165115401166AT55GENIChomozygous119406496
4115401233115401233GGAGTCG58GENIChomozygous128070902
4115401690115401691GC24GENIChomozygous119625065
4115402266115402266AT22GENICheterozygous134993294
4115402267115402268GT24GENIChomozygous119527304
4115404444115404445TC46GENIChomozygous112815456
4115405586115405587CT64GENIChomozygous119406497
4115405686115405687AG51GENIChomozygous119406498
4115406817115406818TC75GENIChomozygous112815460
4115407232115407232TTTTTGT38GENIChomozygous128070904
4115409358115409358G47GENIChomozygous128070905
4115409359115409359CTCTAGAACAC48GENIChomozygous128070906
4115410238115410239TC48GENIChomozygous112815462
4115407974115407974ACCC50GENIChomozygous131359904
4115404071115404072G55GENIChomozygous131359903