| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38231488-38231781 | Rare:129 | ||||
| chr8:38269069-38269334 | Rare:174 | ||||
| chr8:38382155-38382365 | Common:1; Rare:116 | ||||
| chr8:38386270-38386529 | Common:2; Rare:92 | ||||
| chr8:38468578-38468735 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr8:38756784-38757027 | Common:3; Rare:73 | ||||
| chr8:38757155-38757392 | Common:4; Rare:94 | ||||
| chr8:38900790-38901310 | Common:4; Rare:193 | ||||
| chr8:38901598-38901847 | Common:6; Rare:73 | ||||
| chr8:38996417-38997059 | Common:14; Rare:457 | ||||
| chr8:40153317-40153555 | Common:2; Rare:96 | ||||
| chr8:41490350-41490711 | Common:3; Rare:167 | ||||
| chr8:41528908-41529310 | Common:8; Rare:193 | ||||
| chr8:41577939-41578318 | Common:1; Rare:117 | ||||
| chr8:41578374-41578525 | Rare:69 |