chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152459306152459308GT7GENIChomozygous131363804
4152459832152459833TA27GENIChomozygous112888200
4152467609152467610TC14GENIChomozygous112888201
4152473743152473743G21GENIChomozygous128092377
4152475082152475083TC21GENIChomozygous112888204
4152482331152482332AG22GENIChomozygous112888208
4152483554152483554A13GENICheterozygous134685001
4152487560152487560TTCA21GENIChomozygous131363805
4152491270152491270A20GENIChomozygous128092378
4152493552152493553T26GENIChomozygous128092379
4152503264152503265TC19GENIChomozygous112888214
4152505138152505139AG24GENIChomozygous112888216
4152467575152467576AT16GENIChomozygous113397517
4152474876152474877GA15GENIChomozygous113397519
4152479028152479029TA17GENIChomozygous113397521
4152500394152500395GT17GENIChomozygous113397525
4152510554152510555GA27GENIChomozygous112888217
4152512788152512789AG15GENIChomozygous112888219
4152518088152518089AG22GENIChomozygous112888220
4152519838152519839TC22GENIChomozygous112888222
4152530042152530043AT8GENIChomozygous113397529
4152531372152531372AGCCTAAT19GENIChomozygous128092382
4152535294152535295C20GENIChomozygous131363806
4152535297152535302CCTCC22GENIChomozygous131363807
4152550958152550959A24GENICheterozygous128092387
4152551412152551413T30GENIChomozygous131363808
4152557709152557710CT18GENIChomozygous112888238
4152564008152564009AC14GENIChomozygous112888240
4152564733152564733A14GENIChomozygous131363809
4152566824152566825GT15GENIChomozygous112888241
4152567018152567019GA17GENIChomozygous112888242
4152569390152569391A15GENICheterozygous131363810
4152573186152573187GT16GENIChomozygous112888244
4152573535152573536TG24GENIChomozygous113397533
4152576811152576812TC24GENIChomozygous113397535
4152525585152525586GT6GENIChomozygous113307758