chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113486238034862381GA20GENIChomozygous116037397
113486276834862769CT13GENIChomozygous116037399
113486400134864002CA20GENIChomozygous116037401
113487172934871730AG22GENIChomozygous115821077
113487634534876346AC17GENIChomozygous116037403
113487805434878055AG10GENIChomozygous115821086
113488278634882787AG21GENIChomozygous115821092
113488696334886964AG23GENIChomozygous116037405
113489848534898486GT18GENIChomozygous115821104
113490007834900079TC25GENIChomozygous115821106
113490064134900642TA11GENIChomozygous115821108
113490198034901981CT29GENIChomozygous116037407
113490421534904216CT12GENIChomozygous116037409
113491047934910480GA4GENIChomozygous116037413
113491187334911874TC14GENIChomozygous115821114
113491444634914447GA21GENIChomozygous116037415
113491648634916487CT21GENIChomozygous116037417
113492426934924270GA23GENIChomozygous116037419
113492722034927221CT23GENIChomozygous116037421
113492860434928605AC30GENIChomozygous116037423
113492938334929384TC19GENIChomozygous115821122
113493637834936379CT35GENIChomozygous115821130
113494117734941178CA12GENIChomozygous116037427
113494250434942505TG21GENIChomozygous116037429
113494626334946264TC24GENIChomozygous115821148
113494662134946622CT25GENIChomozygous115821150
113494687134946872TA16GENIChomozygous116037431
113495049634950497AG29GENIChomozygous115821156
113495183034951831TG18GENIChomozygous116037433
113495408534954086TC16GENIChomozygous116037435
113495507234955073CT10GENIChomozygous116037437
113495653534956536CT16GENIChomozygous115821166
113495657134956572GT17GENIChomozygous116037439