| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:16870495-16870856 | Common:2; Rare:160 | ||||
| chr9:16870900-16870996 | Common:1; Rare:31 | ||||
| chr9:17134858-17135192 | Common:1; Rare:151 | ||||
| chr9:19049337-19049677 | Common:2; Rare:136 | ||||
| chr9:19102877-19103120 | Common:2; Rare:104 | ||||
| chr9:19127424-19127581 | Common:2; Rare:48 | ||||
| chr9:19127687-19127718 | Rare:12 | ||||
| chr9:19230358-19230833 | Common:8; Rare:206 | ||||
| chr9:19380165-19380373 | Common:5; Rare:104 | ||||
| chr9:20684096-20684282 | Common:3; Rare:75 | ||||
| chr9:21031425-21031699 | Common:3; Rare:113 | ||||
| chr9:21802323-21802687 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994923-21995115 | Common:1; Rare:34 | ||||
| chr9:26892411-26892470 | Rare:27 | ||||
| chr9:26892731-26892865 | Rare:68 |