| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38269161-38269341 | Rare:65 | ||||
| chr8:38901243-38901343 | Rare:22 | ||||
| chr8:38996453-38997078 | Common:7; Rare:236 | ||||
| chr8:40153352-40153640 | Common:2; Rare:89 | ||||
| chr8:41664933-41665289 | Common:2; Rare:102 | ||||
| chr8:41665377-41665487 | Common:1; Rare:18 | ||||
| chr8:42540972-42541189 | Common:1; Rare:57 | ||||
| chr8:42541494-42541752 | Common:2; Rare:79 | ||||
| chr8:42541875-42542052 | Rare:45; Clinvar:3 | ||||
| chr8:42896586-42897028 | Common:1; Rare:179 | ||||
| chr8:43056228-43056476 | Rare:94 | ||||
| chr8:47260824-47260975 | Common:3; Rare:61 | ||||
| chr8:47960097-47960247 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960811-47960964 | Common:1; Rare:58; Clinvar:5 | ||||
| chr8:51898950-51899670 | Common:11; Rare:255 |