| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38386357-38386565 | Rare:50 | ||||
| chr8:38787000-38787244 | Rare:92 | ||||
| chr8:38901052-38901247 | Common:2; Rare:43 | ||||
| chr8:38993598-38993818 | Common:1; Rare:53 | ||||
| chr8:38996261-38996336 | Common:1; Rare:43 | ||||
| chr8:38996455-38997156 | Common:8; Rare:261; Clinvar (benign):1 | ||||
| chr8:40153292-40153861 | Common:3; Rare:177 | ||||
| chr8:41308993-41309147 | Common:2; Rare:57 | ||||
| chr8:41577967-41578269 | Rare:99 | ||||
| chr8:42207467-42207843 | Common:3; Rare:89 | ||||
| chr8:42541070-42541198 | Common:1; Rare:32 | ||||
| chr8:42541486-42541846 | Common:2; Rare:117 | ||||
| chr8:42541852-42542002 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:42843045-42843373 | Common:2; Rare:93; Clinvar:6; Clinvar (benign):4 | ||||
| chr8:42896289-42896471 | Common:2; Rare:90 |