| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:87497640-87497975 | Common:1; Rare:144 | ||||
| chr9:87726024-87726396 | Common:4; Rare:96 | ||||
| chr9:87974521-87974627 | Common:1; Rare:24 | ||||
| chr9:88388276-88388514 | Common:1; Rare:109 | ||||
| chr9:89310959-89311286 | Common:3; Rare:127 | ||||
| chr9:89311414-89311522 | Rare:28 | ||||
| chr9:89318370-89318579 | Common:6; Rare:94 | ||||
| chr9:89318666-89318851 | Rare:53 | ||||
| chr9:91361710-91362002 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:92115330-92115509 | Common:1; Rare:57; Clinvar:1 | ||||
| chr9:92293561-92293903 | Common:6; Rare:108 | ||||
| chr9:92325149-92325228 | Common:2; Rare:11 | ||||
| chr9:92325299-92325996 | Common:9; Rare:189 | ||||
| chr9:92670044-92670406 | Common:1; Rare:112 | ||||
| chr9:92764755-92765016 | Common:2; Rare:90; Clinvar (benign):2 |