| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20658171-20658634 | Common:9; Rare:211 | ||||
| chr9:20658800-20658909 | Rare:24 | ||||
| chr9:20684099-20684283 | Common:3; Rare:74 | ||||
| chr9:20726249-20726501 | Common:1; Rare:53 | ||||
| chr9:21335339-21335526 | Common:3; Rare:68 | ||||
| chr9:23826189-23826499 | Common:1; Rare:126 | ||||
| chr9:26892738-26892927 | Common:1; Rare:89 | ||||
| chr9:26947107-26947571 | Common:2; Rare:155 | ||||
| chr9:27529724-27530014 | Common:5; Rare:74 | ||||
| chr9:27572929-27573010 | Rare:19 | ||||
| chr9:27573411-27573555 | Common:6; Rare:87 | ||||
| chr9:27573709-27573980 | Common:2; Rare:89; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32552557-32552669 | Common:1; Rare:20; Clinvar:2 | ||||
| chr9:32573005-32573271 | Common:4; Rare:95 | ||||
| chr9:33001529-33001775 | Common:3; Rare:120; Clinvar (benign):4 |