chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117086836117086837TC26GENIChomozygous116670874
8117089339117089340TC21GENIChomozygous116670878
8117089635117089636CT33GENIChomozygous116670880
8117089738117089739AG36GENIChomozygous117149344
8117090615117090616CG34GENIChomozygous116670884
8117091949117091950CT39GENIChomozygous116670888
8117092067117092068TC23GENIChomozygous116670890
8117092507117092508CA16GENIChomozygous117149345
8117094276117094277TC18GENIChomozygous116670896
8117094417117094418TG28GENIChomozygous116670898
8117094905117094906TC30GENIChomozygous116670900
8117097502117097503CA31GENIChomozygous116670902
8117098325117098326GA35GENIChomozygous117149346
8117098910117098911AG37GENIChomozygous116670906
8117100426117100427TC22GENIChomozygous116670908
8117102971117102972CT30GENIChomozygous116670910
8117103040117103041AG17GENIChomozygous116670912
8117103195117103196GA18GENIChomozygous116670914
8117109433117109434CT19GENIChomozygous116670922
8117110422117110423CA32GENIChomozygous116670924
8117110798117110799AG19GENIChomozygous117059114
8117110799117110800GC19GENIChomozygous116886916
8117112150117112151GA37GENIChomozygous117149349
8117115178117115179GA28GENIChomozygous116670942
8117115650117115651CA40GENICheterozygous116670954
8117115682117115683TG42GENICheterozygous116670956
8117115701117115702TA45GENICheterozygous116670958
8117115703117115704TG46GENICheterozygous116670960
8117115760117115761GA37GENICheterozygous116670962