| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38105795-38105929 | Rare:40 | ||||
| chr8:38176430-38176881 | Common:5; Rare:129 | ||||
| chr8:38231490-38231781 | Rare:84 | ||||
| chr8:38728008-38728192 | Common:2; Rare:37 | ||||
| chr8:38757229-38757328 | Common:1; Rare:18 | ||||
| chr8:38996469-38996789 | Common:2; Rare:99 | ||||
| chr8:42501125-42501411 | Common:1; Rare:66 | ||||
| chr8:42541102-42541173 | Rare:16 | ||||
| chr8:42541565-42541661 | Rare:32 | ||||
| chr8:42541678-42541892 | Common:1; Rare:72; Clinvar (benign):1 | ||||
| chr8:42843047-42843087 | Rare:10; Clinvar:2 | ||||
| chr8:42843277-42843498 | Common:2; Rare:59; Clinvar (benign):3 | ||||
| chr8:42896573-42897043 | Common:1; Rare:188 | ||||
| chr8:47260736-47260981 | Common:3; Rare:109 | ||||
| chr8:47778762-47778965 | Rare:37; Clinvar:1 |