| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:18651537-18651732 | Common:1; Rare:79 | ||||
| chr10:18659247-18659573 | Common:2; Rare:105 | ||||
| chr10:21526412-21526568 | Common:1; Rare:49 | ||||
| chr10:21533996-21534341 | Common:3; Rare:136 | ||||
| chr10:24209015-24209184 | Rare:50 | ||||
| chr10:25016454-25016608 | Common:3; Rare:47 | ||||
| chr10:27154314-27154452 | Rare:37 | ||||
| chr10:27155194-27155390 | Common:4; Rare:69; Clinvar:3; Clinvar (benign):4 | ||||
| chr10:27240478-27240677 | Common:2; Rare:60 | ||||
| chr10:27242095-27242219 | Common:1; Rare:48 | ||||
| chr10:27504138-27504356 | Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:28532515-28532862 | Common:4; Rare:144 | ||||
| chr10:28532924-28533179 | Common:1; Rare:98 | ||||
| chr10:29522554-29522756 | Rare:57 | ||||
| chr10:29634911-29635061 | Rare:30 |