| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95505857-95506249 | Common:3; Rare:259 | ||||
| chr9:95506380-95506900 | Common:8; Rare:310; Clinvar:29; Clinvar (benign):25; Clinvar (pathogenic):2 | ||||
| chr9:95507386-95507758 | Rare:231 | ||||
| chr9:95875420-95875761 | Common:2; Rare:205 | ||||
| chr9:95875953-95876056 | Common:6; Rare:52 | ||||
| chr9:96383606-96383806 | Common:3; Rare:92 | ||||
| chr9:96418306-96418610 | Common:5; Rare:137 | ||||
| chr9:96566670-96567120 | Common:3; Rare:242 | ||||
| chr9:96619790-96620250 | Common:2; Rare:161 | ||||
| chr9:96654690-96655080 | Common:5; Rare:197 | ||||
| chr9:96655251-96655424 | Common:1; Rare:87 | ||||
| chr9:96778010-96778350 | Common:2; Rare:134 | ||||
| chr9:96854264-96854652 | Common:6; Rare:141 | ||||
| chr9:97013571-97013840 | Common:8; Rare:141 | ||||
| chr9:97039120-97039313 | Common:1; Rare:73 |