| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20684052-20684283 | Common:4; Rare:91 | ||||
| chr9:21031614-21031786 | Common:1; Rare:51 | ||||
| chr9:21335347-21335488 | Common:3; Rare:54 | ||||
| chr9:21802515-21802685 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21995105-21995136 | Rare:12 | ||||
| chr9:21995351-21995472 | Rare:41 | ||||
| chr9:22008695-22008942 | Rare:117 | ||||
| chr9:22009227-22009437 | Common:1; Rare:72 | ||||
| chr9:23735566-23735671 | Rare:31 | ||||
| chr9:23821606-23821903 | Common:3; Rare:130 | ||||
| chr9:23826249-23826499 | Common:1; Rare:101 | ||||
| chr9:24545618-24545998 | Common:4; Rare:132 | ||||
| chr9:26892331-26892514 | Rare:86 | ||||
| chr9:26892691-26892870 | Rare:86 | ||||
| chr9:26947010-26947032 | Rare:5 |