| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:27258380-27258568 | Rare:31 | ||||
| chr8:27311316-27311702 | Common:7; Rare:106 | ||||
| chr8:27490942-27491259 | Common:4; Rare:107 | ||||
| chr8:27611589-27611989 | Common:3; Rare:124 | ||||
| chr8:27614687-27614954 | Rare:88 | ||||
| chr8:27772577-27772775 | Common:6; Rare:62 | ||||
| chr8:27774296-27774586 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:27837762-27837943 | Rare:59 | ||||
| chr8:28092717-28092838 | Common:1; Rare:41 | ||||
| chr8:28092944-28093238 | Common:2; Rare:100 | ||||
| chr8:28093365-28093495 | Rare:26 | ||||
| chr8:28386274-28386674 | Common:16; Rare:159 | ||||
| chr8:28401990-28402530 | Common:9; Rare:149 | ||||
| chr8:28402678-28402805 | Rare:26 | ||||
| chr8:28490174-28490486 | Common:1; Rare:69 |