chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37991825979918260GT30GENIChomozygous111634794
37991973679919737TC12GENIChomozygous111634797
37991985079919851CA14GENIChomozygous111634798
37992094679920947GT21GENIChomozygous111634799
37992164779921648AG19GENIChomozygous111634801
37992244479922445AG10GENIChomozygous111634802
37992158379921584TC12GENIChomozygous112390262
37992357879923579CT6GENIChomozygous112390263
37992612579926126AG12GENIChomozygous111634803
37992679379926794AG9GENICheterozygous111949805
37992798979927990AG5GENIChomozygous111634804
37992806679928067TA22GENIChomozygous111634805
37992860179928602TC5GENICheterozygous111634806
37992903179929032AG11GENIChomozygous111634808
37992938179929382CG18GENIChomozygous111634809
37992958479929585AG7GENIChomozygous111634811
37992958779929588CT10GENIChomozygous111634812
37992993779929938AG17GENIChomozygous111634814
37993064779930648AG15GENIChomozygous111634815
37993222879932229CT11GENIChomozygous111634816
37993253979932540GC16GENIChomozygous111634817
37993469579934696TG6GENIChomozygous111634818
37993490779934908GA9GENIChomozygous111634819
37993586179935862CT11GENIChomozygous111634820
37993586679935867CG13GENIChomozygous111634821
37993606579936066AG12GENIChomozygous111634822
37993659379936594AG16GENIChomozygous111634823
37993673379936734TC18GENIChomozygous111634824
37993690079936901AG17GENIChomozygous111634825
37992680179926802AC7GENIChomozygous119676834
37993499179934992GA10GENIChomozygous120110481
37993041779930418CG11GENICheterozygous125827265