| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33166793-33166956 | Rare:58; Clinvar:2 | ||||
| chr9:33290350-33290565 | Common:2; Rare:79 | ||||
| chr9:33473838-33474143 | Common:4; Rare:94 | ||||
| chr9:33750383-33750690 | Common:1; Rare:81 | ||||
| chr9:34048870-34048973 | Rare:41 | ||||
| chr9:34049186-34049263 | Common:1; Rare:19 | ||||
| chr9:34329228-34329598 | Rare:111 | ||||
| chr9:34458518-34458840 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:34612084-34612177 | Rare:28 | ||||
| chr9:34653787-34653959 | Rare:31 | ||||
| chr9:34662636-34662689 | Rare:23 | ||||
| chr9:34665363-34665665 | Rare:96 | ||||
| chr9:35489901-35490108 | Common:1; Rare:57 | ||||
| chr9:35657750-35657816 | Rare:57; Clinvar:9; Clinvar (pathogenic):5 | ||||
| chr9:35657841-35658449 | Common:11; Rare:476; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 |