| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136805802-136806087 | Rare:56 | ||||
| chr9:136807811-136808187 | Common:3; Rare:135 | ||||
| chr9:136835525-136835695 | Common:1; Rare:43 | ||||
| chr9:136848660-136848827 | Common:1; Rare:46 | ||||
| chr9:136849539-136849754 | Common:1; Rare:83 | ||||
| chr9:136886267-136886531 | Common:2; Rare:77 | ||||
| chr9:136944592-136944909 | Common:2; Rare:123 | ||||
| chr9:136996556-136996708 | Common:1; Rare:44 | ||||
| chr9:137012806-137013091 | Common:1; Rare:102 | ||||
| chr9:137053881-137054210 | Common:1; Rare:114 | ||||
| chr9:137086628-137087121 | Common:2; Rare:201; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137114688-137114984 | Common:2; Rare:120 | ||||
| chr9:137175882-137176109 | Common:3; Rare:66 | ||||
| chr9:137188541-137188744 | Common:2; Rare:101 | ||||
| chr9:137188923-137189247 | Rare:116 |