| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102528872-102529132 | Common:2; Rare:60 | ||||
| chr8:104725490-104725812 | Common:2; Rare:55 | ||||
| chr8:116856197-116856431 | Rare:62; Clinvar:1 | ||||
| chr8:144700549-144700686 | Common:1; Rare:34 | ||||
| chr8:145002835-145002968 | Common:1; Rare:39 | ||||
| chr9:8858537-8858666 | Rare:35 | ||||
| chr9:9441787-9442060 | Common:4; Rare:66 | ||||
| chr9:14993193-14993330 | Common:2; Rare:46 | ||||
| chr9:15468961-15469185 | Common:2; Rare:63 | ||||
| chr9:19789029-19789127 | Common:3; Rare:34 | ||||
| chr9:32550824-32551144 | Common:1; Rare:127; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35749984-35750089 | Rare:20 | ||||
| chr9:39464487-39464685 | Rare:47 | ||||
| chr9:39809851-39810002 | Common:1; Rare:6 | ||||
| chr9:40991944-40992356 | Common:7; Rare:33 |