| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15422544-15422888 | Common:1; Rare:147 | ||||
| chr9:15552832-15552910 | Common:1; Rare:29 | ||||
| chr9:17134909-17135197 | Common:1; Rare:138 | ||||
| chr9:19049291-19049447 | Rare:69 | ||||
| chr9:19102863-19103030 | Common:1; Rare:67 | ||||
| chr9:19127458-19127568 | Common:1; Rare:29 | ||||
| chr9:19380191-19380353 | Common:4; Rare:79 | ||||
| chr9:21031623-21031691 | Common:1; Rare:21 | ||||
| chr9:21802323-21802685 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994344-21994832 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:21995039-21995121 | Common:1; Rare:19 | ||||
| chr9:26892731-26892913 | Common:1; Rare:85 | ||||
| chr9:26947117-26947294 | Rare:64 | ||||
| chr9:26956351-26956472 | Common:2; Rare:42 | ||||
| chr9:32573064-32573190 | Common:2; Rare:50 |