| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:27311273-27311567 | Common:6; Rare:100 | ||||
| chr8:28701333-28701613 | Common:3; Rare:100 | ||||
| chr8:30095249-30095507 | Common:2; Rare:80 | ||||
| chr8:30156243-30156386 | Rare:40 | ||||
| chr8:33484981-33485193 | Common:5; Rare:71 | ||||
| chr8:38030338-38030581 | Common:3; Rare:73 | ||||
| chr8:38105396-38105550 | Common:2; Rare:48 | ||||
| chr8:38176448-38176857 | Common:5; Rare:108 | ||||
| chr8:38269167-38269247 | Rare:31 | ||||
| chr8:38996520-38996781 | Common:2; Rare:69 | ||||
| chr8:42391697-42391920 | Common:3; Rare:79 | ||||
| chr8:42541013-42541170 | Rare:41 | ||||
| chr8:42541565-42541661 | Rare:32 | ||||
| chr8:42541700-42541920 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr8:42896697-42897027 | Common:1; Rare:129 |