chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117455782117455783GA45GENIChomozygous808327858
8117460914117460915GT59GENIChomozygous808327859
8117462354117462355CT55GENIChomozygous808327860
8117463142117463143AG36GENIChomozygous808327861
8117463763117463764CT50GENIChomozygous808327862
8117464369117464370AG18GENIChomozygous808327863
8117464395117464396CG22GENIChomozygous808327864
8117464601117464602TC70GENICpossibly homozygous808327865
8117464876117464877GA39GENIChomozygous808327866
8117466249117466250AC46GENICpossibly homozygous808327867
8117466513117466514TC52GENIChomozygous808327868
8117467475117467476TG32GENICpossibly homozygous808327869
8117467952117467953AG30GENIChomozygous808327870
8117468441117468442GA41GENIChomozygous808327871
8117468564117468565GA41GENIChomozygous808327872
8117468864117468865CG33GENIChomozygous808327873
8117469362117469363TC66GENIChomozygous808327874
8117470014117470015TC52GENIChomozygous808327875
8117470387117470388GA29GENIChomozygous808327876
8117470450117470451GC28GENIChomozygous808327877
8117471283117471284TC52GENIChomozygous808327878
8117471357117471358AT52GENICpossibly homozygous808327879
8117471931117471932TG40GENIChomozygous808327880
8117471948117471949GT32GENICheterozygous808327881
8117471956117471957GT26GENIChomozygous808327882
8117472015117472016TC32GENIChomozygous808327883
8117473215117473216GA44GENIChomozygous808327884
8117473789117473790AG20GENICheterozygous808327885
8117473838117473839GA48GENICheterozygous808327886
8117473873117473874GA61GENICheterozygous808327887
8117473895117473896AC65GENICheterozygous808327888
8117473918117473919AT74GENICheterozygous808327889
8117473986117473987CT110GENICheterozygous808327890
8117474020117474021AG128GENICheterozygous808327891
8117475110117475111CA44GENIChomozygous808327892