| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42542135-42542302 | Common:2; Rare:45; Clinvar (benign):1 | ||||
| chr8:42896596-42897122 | Common:1; Rare:203 | ||||
| chr8:43056132-43056476 | Common:1; Rare:124 | ||||
| chr8:43140297-43140592 | Common:3; Rare:113; Clinvar:10 | ||||
| chr8:47260781-47260981 | Common:3; Rare:87 | ||||
| chr8:47960112-47960267 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr8:47960811-47960974 | Common:1; Rare:65; Clinvar:6 | ||||
| chr8:51898955-51899331 | Common:7; Rare:165 | ||||
| chr8:51899574-51899726 | Rare:37 | ||||
| chr8:52714316-52714597 | Common:1; Rare:115 | ||||
| chr8:54022246-54022510 | Common:1; Rare:84 | ||||
| chr8:55773306-55773552 | Common:3; Rare:86 | ||||
| chr8:56074358-56074717 | Common:6; Rare:148 | ||||
| chr8:58659616-58659777 | Rare:53 | ||||
| chr8:60516843-60517253 | Common:1; Rare:125 |