chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109021144190211442GA14GENIChomozygous68165194
109021235690212357GA9GENIChomozygous68165197
109021430390214306TTG10GENICheterozygous69277024
109021491290214913TA9GENIChomozygous68165200
109021515490215155GA17GENIChomozygous68165203
109021696190216962TC7GENIChomozygous68165206
109021747590217476GT5GENIChomozygous69277030
109021990690219907CA9GENIChomozygous68165210
109021993590219936CG4GENIChomozygous68165213
109022031190220312GA14GENIChomozygous68165225
109022155490221555AC12GENIChomozygous68165228
109022178290221783AG15GENIChomozygous68165231
109022243490222435TC15GENIChomozygous68165234
109022272390222724CT15GENIChomozygous68165237
109022287390222874AG6GENIChomozygous69277038
109022302390223024AG16GENIChomozygous68165240
109022416190224162CT11GENIChomozygous68165246
109022417390224174AG8GENIChomozygous68165249
109022758490227585TC4GENIChomozygous68165259
109022775490227755TG5GENIChomozygous68165262
109022903390229034AG16GENIChomozygous68165265
109022912790229128AG11GENIChomozygous68165268
109021808190218081T9GENIChomozygous69437406
109022287390222873G16GENICheterozygous69437407
109022709690227097A4GENIChomozygous69437409
109023152190231522GC13GENIChomozygous68165271
109023180590231806GC12GENIChomozygous68165274
109023218790232188A9GENICheterozygous69277046
109023304490233045TC27GENIChomozygous68165277
109023463690234637AG22GENIChomozygous68165286
109023468590234686AG14GENIChomozygous68165289
109023634090236341CT7GENIChomozygous68165292