| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136746183-136746455 | Common:2; Rare:42 | ||||
| chr9:136800129-136800392 | Common:5; Rare:82 | ||||
| chr9:136807768-136808178 | Common:3; Rare:154 | ||||
| chr9:136848660-136848789 | Rare:37 | ||||
| chr9:136849585-136849868 | Common:1; Rare:97 | ||||
| chr9:136849922-136850126 | Common:1; Rare:83 | ||||
| chr9:136886232-136886540 | Common:2; Rare:95 | ||||
| chr9:136944592-136944866 | Common:1; Rare:110 | ||||
| chr9:136949443-136949644 | Rare:43 | ||||
| chr9:136952165-136952705 | Common:2; Rare:136 | ||||
| chr9:136996510-136996676 | Common:1; Rare:52 | ||||
| chr9:136996679-136996842 | Common:1; Rare:42 | ||||
| chr9:137019041-137019250 | Rare:78 | ||||
| chr9:137028154-137028495 | Common:1; Rare:103 | ||||
| chr9:137086658-137087131 | Common:2; Rare:194; Clinvar:5; Clinvar (benign):1 |