| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:10054647-10054851 | Common:1; Rare:111 | ||||
| chr8:10839789-10840116 | Common:3; Rare:109 | ||||
| chr8:11201371-11201582 | Common:3; Rare:70 | ||||
| chr8:11201825-11201973 | Common:1; Rare:48 | ||||
| chr8:11284746-11284896 | Common:3; Rare:73 | ||||
| chr8:11466733-11466944 | Common:2; Rare:81 | ||||
| chr8:11467590-11467776 | Rare:60 | ||||
| chr8:11769569-11769781 | Common:5; Rare:92 | ||||
| chr8:11802356-11802806 | Common:9; Rare:270 | ||||
| chr8:13514728-13515018 | Common:1; Rare:69 | ||||
| chr8:13566735-13566961 | Common:6; Rare:82 | ||||
| chr8:15540182-15540363 | Common:4; Rare:65; Clinvar:8; Clinvar (benign):1 | ||||
| chr8:15561452-15561643 | Common:2; Rare:65 | ||||
| chr8:17027149-17027261 | Common:2; Rare:60 | ||||
| chr8:17246777-17247048 | Common:2; Rare:116 |