| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:83979602-83979746 | Rare:87 | ||||
| chr9:83980160-83980361 | Rare:129 | ||||
| chr9:83980552-83980844 | Common:5; Rare:126 | ||||
| chr9:85940818-85941367 | Common:9; Rare:298 | ||||
| chr9:86281960-86282270 | Common:10; Rare:187 | ||||
| chr9:86282456-86282714 | Common:6; Rare:209 | ||||
| chr9:86354315-86354614 | Rare:199 | ||||
| chr9:87497655-87498040 | Common:5; Rare:317 | ||||
| chr9:87725909-87726225 | Common:6; Rare:92 | ||||
| chr9:88388232-88388497 | Common:2; Rare:212 | ||||
| chr9:89310742-89311237 | Common:11; Rare:330 | ||||
| chr9:89318379-89318565 | Common:6; Rare:83 | ||||
| chr9:89318598-89318998 | Common:2; Rare:215 | ||||
| chr9:91355739-91356301 | Common:8; Rare:242; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr9:91361060-91361610 | Common:1; Rare:196 |