| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17229121-17229348 | Common:1; Rare:45 | ||||
| chr10:17643885-17644269 | Common:2; Rare:115 | ||||
| chr10:18651553-18651693 | Common:1; Rare:54 | ||||
| chr10:18659259-18659577 | Common:2; Rare:103 | ||||
| chr10:22316261-22316459 | Rare:87 | ||||
| chr10:22321397-22321600 | Rare:69 | ||||
| chr10:24722584-24722836 | Rare:63 | ||||
| chr10:26216090-26216377 | Common:2; Rare:62 | ||||
| chr10:27100427-27100557 | Common:2; Rare:44; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154301-27154474 | Rare:45 | ||||
| chr10:27242068-27242228 | Common:1; Rare:70 | ||||
| chr10:27504138-27504356 | Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:28532491-28532862 | Common:5; Rare:148 | ||||
| chr10:30059503-30059671 | Common:1; Rare:64 | ||||
| chr10:31031848-31032025 | Common:1; Rare:69 |