| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541923-42542093 | Common:1; Rare:44; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42843029-42843116 | Rare:26; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr8:42843248-42843527 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896596-42897037 | Common:1; Rare:179 | ||||
| chr8:43056153-43056470 | Common:1; Rare:120 | ||||
| chr8:47960068-47960252 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:47960683-47961000 | Common:2; Rare:121; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:48008339-48008454 | Common:2; Rare:73 | ||||
| chr8:53843207-53843358 | Rare:37 | ||||
| chr8:54022261-54022511 | Common:1; Rare:79 | ||||
| chr8:54135154-54135284 | Common:2; Rare:44 | ||||
| chr8:55773289-55773497 | Common:3; Rare:66 | ||||
| chr8:56074357-56074652 | Common:4; Rare:128 | ||||
| chr8:58659629-58659816 | Common:2; Rare:61 | ||||
| chr8:59119196-59119270 | Rare:21 |