| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:33485033-33485211 | Common:2; Rare:61 | ||||
| chr8:38030281-38030580 | Common:3; Rare:86 | ||||
| chr8:38105441-38105540 | Common:1; Rare:32 | ||||
| chr8:38176449-38176863 | Common:5; Rare:112 | ||||
| chr8:38996473-38996789 | Common:2; Rare:98 | ||||
| chr8:42152781-42153074 | Common:1; Rare:76 | ||||
| chr8:42391808-42391917 | Common:1; Rare:38 | ||||
| chr8:42541467-42541661 | Common:2; Rare:50 | ||||
| chr8:42541691-42541999 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:42843277-42843477 | Common:2; Rare:54; Clinvar (benign):3 | ||||
| chr8:42896596-42896978 | Common:1; Rare:162 | ||||
| chr8:47260853-47260981 | Common:3; Rare:53 | ||||
| chr8:47960127-47960267 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr8:47960683-47960974 | Common:2; Rare:111; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:48008354-48008448 | Common:1; Rare:60 |