| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38176430-38176867 | Common:5; Rare:124 | ||||
| chr8:38996452-38997003 | Common:7; Rare:202 | ||||
| chr8:41577985-41578249 | Rare:82 | ||||
| chr8:42541131-42541173 | Rare:8 | ||||
| chr8:42541559-42541661 | Rare:34 | ||||
| chr8:42541700-42541897 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr8:43056206-43056476 | Rare:104 | ||||
| chr8:47260765-47260975 | Common:3; Rare:94 | ||||
| chr8:47960122-47960267 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr8:47960808-47960983 | Common:1; Rare:68; Clinvar:6 | ||||
| chr8:48008350-48008448 | Common:2; Rare:61 | ||||
| chr8:53843217-53843328 | Rare:25 | ||||
| chr8:55773341-55773497 | Common:3; Rare:51 | ||||
| chr8:56074412-56074602 | Common:3; Rare:94 | ||||
| chr8:59119069-59119245 | Rare:40 |