| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:30560056-30560258 | Common:1; Rare:45 | ||||
| chr8:30561230-30561494 | Rare:64 | ||||
| chr8:30566188-30566337 | Rare:33 | ||||
| chr8:30567674-30567872 | Common:1; Rare:42 | ||||
| chr8:30568928-30569116 | Rare:40 | ||||
| chr8:30569218-30569579 | Common:2; Rare:84 | ||||
| chr8:30582887-30583118 | Common:3; Rare:37 | ||||
| chr8:30583537-30583874 | Common:4; Rare:61 | ||||
| chr8:30624011-30624234 | Common:1; Rare:53 | ||||
| chr8:33490173-33490337 | Rare:34 | ||||
| chr8:33495346-33495604 | Rare:46 | ||||
| chr8:37744194-37744696 | Common:1; Rare:117; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:37748000-37748148 | Rare:47 | ||||
| chr8:37753275-37753528 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:37903477-37903619 | Rare:14 |