chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152455208152455209A14GENICheterozygous133132266
4152459832152459833TA44GENIChomozygous112888200
4152467609152467610TC52GENIChomozygous112888201
4152473743152473743G48GENIChomozygous128092377
4152475082152475083TC62GENIChomozygous112888204
4152482331152482332AG55GENIChomozygous112888208
4152459306152459308GT20GENIChomozygous131363804
4152487560152487560TTCA48GENIChomozygous131363805
4152467575152467576AT58GENIChomozygous113397517
4152474876152474877GA61GENIChomozygous113397519
4152479028152479029TA64GENIChomozygous113397521
4152491270152491270A63GENIChomozygous128092378
4152493552152493553T40GENICpossibly homozygous128092379
4152500394152500395GT66GENIChomozygous113397525
4152503264152503265TC57GENIChomozygous112888214
4152505138152505139AG39GENIChomozygous112888216
4152509397152509397A24GENICheterozygous132396631
4152510554152510555GA52GENIChomozygous112888217
4152512788152512789AG47GENIChomozygous112888219
4152518088152518089AG40GENIChomozygous112888220
4152519838152519839TC44GENIChomozygous112888222
4152530042152530043AT31GENIChomozygous113397529
4152531372152531372AGCCTAAT42GENIChomozygous128092382
4152550958152550959A30GENICheterozygous128092387
4152551412152551413T36GENIChomozygous131363808
4152557709152557710CT57GENIChomozygous112888238
4152564008152564009AC49GENIChomozygous112888240
4152564733152564733A26GENICpossibly homozygous131363809
4152566824152566825GT38GENIChomozygous112888241
4152567018152567019GA45GENIChomozygous112888242
4152569390152569391A38GENICpossibly homozygous131363810
4152573186152573187GT18GENIChomozygous112888244
4152573535152573536TG40GENIChomozygous113397533
4152576811152576812TC42GENIChomozygous113397535
4152534668152534668A29GENICheterozygous130939249
4152525585152525586GT19GENIChomozygous113307758