chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101417537414175375AC21GENIChomozygous116736790
101417564114175642AG20GENIChomozygous116736791
101417591314175914AG18GENIChomozygous116736793
101417717714177178TC2GENIChomozygous116915861
101417751314177514CA21GENIChomozygous116736794
101417776514177766CT18GENIChomozygous116736795
101417976414179765CT28GENIChomozygous116736796
101417976614179767TC28GENIChomozygous116736797
101418033314180334TC23GENIChomozygous116736799
101418085614180857AG26GENIChomozygous116736800
101418104914181050CT24GENIChomozygous116736801
101418408914184090TG32GENIChomozygous116736806
101418200314182004CT20GENIChomozygous116736803
101418373714183738GT21GENIChomozygous116736804
101418405814184059TC24GENIChomozygous116736805
101418410114184102TA36GENIChomozygous116736807
101418527814185279CT16GENIChomozygous116915863
101419188814191889CT26GENIChomozygous116736809
101419218414192185AG10GENIChomozygous116736810
101419242814192429AC31GENIChomozygous116736811
101419261614192617TC29GENIChomozygous116736812
101419379814193799GT21GENIChomozygous116915865
101419380014193801TG23GENIChomozygous116915867
101419420714194208CT24GENIChomozygous116915869
101419695014196951AG14GENIChomozygous116736815
101419773114197732AG14GENIChomozygous116915871
101419785014197851TC24GENIChomozygous116736816
101419793014197931TC20GENIChomozygous116736817
101419878714198788TA16GENIChomozygous116736818
101420247714202478CT27GENIChomozygous116736820
101420298514202986TC29GENIChomozygous116736821
101420302814203029GA30GENIChomozygous116736822
101420316514203166AG25GENIChomozygous116736823
101420435314204354GT34GENIChomozygous116736824
101420489914204900GA16GENIChomozygous116915873
101420563614205637GT21GENIChomozygous116736827
101420597714205978AC21GENIChomozygous116915875