chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152459306152459308GT17GENIChomozygous131363804
4152459832152459833TA68GENIChomozygous112888200
4152467575152467576AT71GENIChomozygous113397517
4152467609152467610TC71GENIChomozygous112888201
4152473743152473743G40GENIChomozygous128092377
4152474876152474877GA61GENIChomozygous113397519
4152475082152475083TC56GENIChomozygous112888204
4152479028152479029TA53GENIChomozygous113397521
4152482331152482332AG55GENIChomozygous112888208
4152487560152487560TTCA49GENIChomozygous131363805
4152491270152491270A53GENIChomozygous128092378
4152493552152493553T50GENIChomozygous128092379
4152500394152500395GT70GENIChomozygous113397525
4152503264152503265TC58GENIChomozygous112888214
4152505138152505139AG56GENICpossibly homozygous112888216
4152510554152510555GA52GENIChomozygous112888217
4152512788152512789AG67GENIChomozygous112888219
4152518088152518089AG50GENIChomozygous112888220
4152519838152519839TC54GENIChomozygous112888222
4152525585152525586GT17GENICpossibly homozygous113307758
4152530042152530043AT29GENIChomozygous113397529
4152531372152531372AGCCTAAT51GENIChomozygous128092382
4152535294152535295C15GENIChomozygous131363806
4152535297152535302CCTCC16GENIChomozygous131363807
4152551412152551413T58GENIChomozygous131363808
4152557709152557710CT50GENIChomozygous112888238
4152564008152564009AC48GENIChomozygous112888240
4152564733152564733A29GENIChomozygous131363809
4152566824152566825GT42GENIChomozygous112888241
4152567018152567019GA55GENIChomozygous112888242
4152569390152569391A44GENICpossibly homozygous131363810
4152573186152573187GT26GENIChomozygous112888244
4152573535152573536TG60GENIChomozygous113397533
4152532991152532992GC28GENICheterozygous131646340
4152532995152532996CT26GENICheterozygous131646341
4152532996152532997GA25GENICheterozygous131646342
4152576811152576812TC56GENIChomozygous113397535