| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23706529-23706704 | Rare:47; Clinvar (benign):1 | ||||
| chr8:23706710-23707158 | Common:3; Rare:86 | ||||
| chr8:23854754-23854829 | Rare:19 | ||||
| chr8:25459144-25459291 | Common:2; Rare:59 | ||||
| chr8:26382916-26383133 | Common:3; Rare:95 | ||||
| chr8:26383224-26383429 | Rare:69 | ||||
| chr8:26513874-26514163 | Common:1; Rare:62 | ||||
| chr8:27311236-27311521 | Common:7; Rare:105 | ||||
| chr8:27614683-27614947 | Rare:88 | ||||
| chr8:27772544-27772747 | Common:7; Rare:73 | ||||
| chr8:27837729-27837929 | Common:1; Rare:60 | ||||
| chr8:28092814-28093219 | Common:4; Rare:118 | ||||
| chr8:28386408-28386517 | Common:8; Rare:29 | ||||
| chr8:28490207-28490448 | Common:1; Rare:49 | ||||
| chr8:28494107-28494334 | Common:5; Rare:76 |