| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23682902-23683065 | Common:1; Rare:51 | ||||
| chr8:24956610-24956742 | Common:2; Rare:31 | ||||
| chr8:25458217-25458608 | Common:2; Rare:108 | ||||
| chr8:25458783-25459378 | Common:5; Rare:188 | ||||
| chr8:26045359-26045579 | Common:2; Rare:82 | ||||
| chr8:26298456-26298600 | Rare:37 | ||||
| chr8:26382865-26383264 | Common:3; Rare:165 | ||||
| chr8:26383281-26383671 | Common:2; Rare:97 | ||||
| chr8:26513874-26514051 | Common:1; Rare:33 | ||||
| chr8:26854655-26854819 | Rare:23 | ||||
| chr8:27311206-27311683 | Common:10; Rare:161 | ||||
| chr8:27610474-27610747 | Common:1; Rare:88 | ||||
| chr8:27772517-27772703 | Common:5; Rare:65 | ||||
| chr8:27774381-27774599 | Common:2; Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:27837713-27838153 | Common:3; Rare:114 |