chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14186326741863268AG30GENIChomozygous74992151
14186327141863272TC31GENIChomozygous74992152
14186382441863825AG19GENIChomozygous74992153
14186390741863908GC22GENIChomozygous74992154
14186457041864571AG16GENIChomozygous74992155
14186464241864643AG12GENIChomozygous74992156
14186467941864680TG17GENIChomozygous74992157
14186493041864931AT24GENIChomozygous74992158
14186494641864947GA24GENIChomozygous74992159
14186499241864993CT17GENIChomozygous74992160
14186559041865591TA22GENIChomozygous74992161
14186574041865741CT15GENICpossibly homozygous74992162
14186579741865798AC14GENICheterozygous74992163
14186593741865938AG15GENIChomozygous74992164
14186690041866901AT15GENIChomozygous74992165
14186575041865751CA10GENICheterozygous76678181
14186736141867362GC23GENIChomozygous74992166
14186766041867661CG23GENIChomozygous74992167
14186777541867776AG28GENIChomozygous74992168
14186791741867918TG16GENIChomozygous74992169
14186810741868108TC18GENIChomozygous74992170
14186842341868424CA18GENIChomozygous74992171
14186899641868997GA18GENIChomozygous74992172
14186981141869812GC21GENIChomozygous74992173