| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97982970-97983370 | Common:1; Rare:157 | ||||
| chr9:97984139-97984294 | Common:1; Rare:72 | ||||
| chr9:97984580-97985030 | Common:4; Rare:197 | ||||
| chr9:98056528-98056780 | Common:1; Rare:86 | ||||
| chr9:98119396-98119639 | Common:1; Rare:36 | ||||
| chr9:98192617-98192884 | Common:6; Rare:72 | ||||
| chr9:98255560-98255910 | Common:3; Rare:110 | ||||
| chr9:98796501-98796704 | Common:1; Rare:71 | ||||
| chr9:98807517-98807677 | Common:2; Rare:46 | ||||
| chr9:99038486-99038650 | Common:2; Rare:59 | ||||
| chr9:99104764-99105188 | Common:2; Rare:136; Clinvar (benign):1 | ||||
| chr9:99221968-99222343 | Common:2; Rare:135 | ||||
| chr9:99821678-99821887 | Rare:66 | ||||
| chr9:99906544-99906815 | Common:1; Rare:109 | ||||
| chr9:100098974-100099325 | Common:2; Rare:98; Clinvar:2 |