| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:134421414-134421701 | Common:1; Rare:68 | ||||
| chr9:134811386-134811598 | Rare:66; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:136400139-136400328 | Common:2; Rare:64 | ||||
| chr9:136646541-136646684 | Common:2; Rare:34 | ||||
| chr9:136647150-136647262 | Common:1; Rare:21 | ||||
| chr9:136659382-136659445 | Common:1; Rare:17 | ||||
| chr9:136671685-136672048 | Common:1; Rare:114 | ||||
| chr9:136842297-136842498 | Common:1; Rare:55 | ||||
| chr9:136847844-136848069 | Rare:50 | ||||
| chr9:136854229-136854573 | Rare:119 | ||||
| chr9:136862933-136863223 | Common:2; Rare:82 | ||||
| chr9:136941555-136941813 | Common:1; Rare:131 | ||||
| chr9:136950074-136950185 | Rare:38 | ||||
| chr9:137032011-137032141 | Common:1; Rare:36 | ||||
| chr9:137223385-137223689 | Common:3; Rare:105 |