chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3152400125152400126GA55GENIChomozygous136840835
3152401296152401297C73GENIChomozygous136595976
3152404271152404272TC68GENIChomozygous136840836
3152404858152404858C63GENIChomozygous136595977
3152404942152404943AC59GENIChomozygous136840837
3152405709152405710TC50GENIChomozygous136840838
3152407994152407995TC62GENIChomozygous136840839
3152408094152408095CT48GENIChomozygous136840840
3152408215152408216TC50GENIChomozygous136840841
3152408728152408729GA51GENIChomozygous136840842
3152408896152408897AG41GENIChomozygous136840843
3152409181152409193CACCAAGACAGT53GENIChomozygous136595978
3152409819152409823GAAG50GENIChomozygous136595979
3152410541152410542TC60GENIChomozygous136840844
3152410879152410880AG55GENIChomozygous136840845
3152410964152410965GA42GENIChomozygous136840846
3152412577152412577C51GENIChomozygous136595980
3152412900152412901A68GENIChomozygous136595981
3152413093152413094AT59GENICpossibly homozygous136840847
3152414788152414789TC58GENIChomozygous136840848
3152416309152416310TA38GENIChomozygous136840849
3152416313152416314TA39GENIChomozygous136840850
3152417778152417779CT52GENIChomozygous136840851
3152417833152417834GA62GENIChomozygous136840852
3152417868152417869GA52GENIChomozygous136840853
3152418902152418903CT53GENIChomozygous136840854
3152419632152419633CT62GENIChomozygous136840855
3152420169152420170TA22GENIChomozygous136840856
3152420171152420172TA22GENIChomozygous136840857
3152420173152420174TA23GENIChomozygous136840858
3152420175152420176TA8GENICheterozygous136840859
3152422830152422831TA68GENIChomozygous136840860
3152416224152416228TCCT13GENIChomozygous146071037
3152408509152408510C18GENICheterozygous403082562
3152408509152408510CT18GENIChomozygous403082563
3152420169152420170T22GENICheterozygous403082564