chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14186326741863268AG33GENIChomozygous74992151
14186327141863272TC33GENIChomozygous74992152
14186382441863825AG30GENIChomozygous74992153
14186390741863908GC24GENIChomozygous74992154
14186457041864571AG15GENIChomozygous74992155
14186464241864643AG16GENIChomozygous74992156
14186467941864680TG18GENIChomozygous74992157
14186493041864931AT15GENIChomozygous74992158
14186494641864947GA18GENIChomozygous74992159
14186499241864993CT28GENIChomozygous74992160
14186559041865591TA40GENIChomozygous74992161
14186574041865741CT26GENICheterozygous74992162
14186579741865798AC22GENICheterozygous74992163
14186593741865938AG20GENIChomozygous74992164
14186690041866901AT43GENIChomozygous74992165
14186736141867362GC35GENIChomozygous74992166
14186766041867661CG31GENIChomozygous74992167
14186777541867776AG31GENIChomozygous74992168
14186791741867918TG16GENIChomozygous74992169
14186810741868108TC30GENIChomozygous74992170
14186842341868424CA23GENIChomozygous74992171
14186899641868997GA35GENIChomozygous74992172
14186981141869812GC29GENIChomozygous74992173