| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38467983-38468127 | Rare:41; Clinvar (benign):1 | ||||
| chr8:38757155-38757407 | Common:2; Rare:58 | ||||
| chr8:38786984-38787272 | Rare:109 | ||||
| chr8:38996231-38996336 | Common:1; Rare:54 | ||||
| chr8:38996441-38996892 | Common:5; Rare:151 | ||||
| chr8:38996896-38997156 | Common:3; Rare:116; Clinvar (benign):1 | ||||
| chr8:38997400-38997546 | Common:1; Rare:40 | ||||
| chr8:40153446-40154336 | Common:5; Rare:235 | ||||
| chr8:42051976-42052266 | Common:1; Rare:84 | ||||
| chr8:42271248-42271447 | Common:1; Rare:70 | ||||
| chr8:42319029-42319218 | Rare:23 | ||||
| chr8:42391795-42391925 | Common:1; Rare:43 | ||||
| chr8:42534454-42534718 | Common:4; Rare:41 | ||||
| chr8:42541131-42541249 | Common:1; Rare:25 | ||||
| chr8:42541494-42541869 | Common:3; Rare:126; Clinvar (benign):1 |