Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:95018439-95018616 | Rare:28 | ||||
chr9:95048368-95048660 | Rare:70 | ||||
chr9:95506534-95506672 | Rare:51; Clinvar:7; Clinvar (benign):7 | ||||
chr9:95507374-95507466 | Rare:27 | ||||
chr9:95509131-95509217 | Rare:24 | ||||
chr9:95516939-95517243 | Common:3; Rare:68 | ||||
chr9:95875453-95875703 | Common:1; Rare:82 | ||||
chr9:95875965-95876058 | Common:5; Rare:47; Clinvar (pathogenic):1 | ||||
chr9:96655307-96655408 | Rare:24 | ||||
chr9:96778054-96778154 | Rare:32 | ||||
chr9:97633271-97633830 | Common:6; Rare:170 | ||||
chr9:97666556-97666817 | Common:1; Rare:42 | ||||
chr9:98056576-98056777 | Common:1; Rare:69 | ||||
chr9:98119188-98119322 | Common:1; Rare:33 | ||||
chr9:98255557-98255909 | Common:3; Rare:109 |