chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132690341926903420GA24GENIChomozygous890417870
132690455026904551TG12GENIChomozygous890417871
132690487426904875TC20GENIChomozygous890417872
132690502526905026TC14GENIChomozygous890417873
132690512426905125CT6GENICheterozygous890417874
132690579726905798AG13GENICheterozygous890417875
132690619126906192GC6GENICheterozygous890417876
132690621526906216CA4GENICheterozygous890417877
132690646326906464AC16GENIChomozygous890417878
132690772226907723CT15GENIChomozygous890417879
132690799526907996CT14GENIChomozygous890417880
132690806426908065TC8GENIChomozygous890417881
132690829026908291GA8GENIChomozygous890417882
132690871226908713TC12GENIChomozygous890417883
132690888826908889CG23GENIChomozygous890417884
132690930926909310CT32GENIChomozygous890417885
132690957626909577CA3GENICheterozygous890417886
132691026926910270GC12GENIChomozygous890417887
132691093226910933GT8GENIChomozygous890417888
132691109026911091GA17GENIChomozygous890417889
132691133226911333GA9GENIChomozygous890417890
132691164826911649CT20GENIChomozygous890417891
132691245026912451TG16GENIChomozygous890417892
132691366226913663GA24GENIChomozygous890417893
132691717726917178CT8GENIChomozygous890417894
132691867226918673CT21GENIChomozygous890417895
132692003926920040AG19GENIChomozygous890417896
132692122326921224CT15GENIChomozygous890417897
132692176126921762TC11GENIChomozygous890417898
132692232326922324GA16GENIChomozygous890417899
132692238526922386AT14GENIChomozygous890417900
132692256126922562TC10GENIChomozygous890417901
132692257626922577CA8GENIChomozygous890417902
132692271526922716AC16GENIChomozygous890417903
132692276726922768AG20GENIChomozygous890417904