| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37736326-37736763 | Common:3; Rare:153 | ||||
| chr8:37736822-37736988 | Rare:35 | ||||
| chr8:37762342-37762708 | Common:2; Rare:129 | ||||
| chr8:37783704-37784104 | Rare:118 | ||||
| chr8:37849830-37850056 | Common:2; Rare:76 | ||||
| chr8:37899481-37899714 | Common:2; Rare:95 | ||||
| chr8:38030236-38030581 | Common:4; Rare:95 | ||||
| chr8:38104850-38105250 | Common:10; Rare:149 | ||||
| chr8:38105259-38105562 | Common:2; Rare:87 | ||||
| chr8:38105692-38105960 | Common:1; Rare:87 | ||||
| chr8:38150580-38150870 | Rare:92; Clinvar (pathogenic):2 | ||||
| chr8:38150890-38151220 | Common:1; Rare:65; Clinvar:2 | ||||
| chr8:38176439-38176886 | Common:6; Rare:126 | ||||
| chr8:38231485-38231813 | Rare:93 | ||||
| chr8:38232189-38232291 | Rare:31 |