| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27100427-27100549 | Common:1; Rare:43; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154176-27154495 | Rare:89 | ||||
| chr10:27155161-27155448 | Common:7; Rare:120; Clinvar:5; Clinvar (benign):7 | ||||
| chr10:27240372-27240601 | Rare:70 | ||||
| chr10:27240711-27240910 | Rare:52 | ||||
| chr10:27241864-27242241 | Common:2; Rare:133 | ||||
| chr10:27414344-27414505 | Common:1; Rare:41 | ||||
| chr10:27504116-27504367 | Rare:132; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:27743510-27743578 | Rare:17 | ||||
| chr10:27981833-27981987 | Common:4; Rare:30 | ||||
| chr10:28282091-28282206 | Common:1; Rare:21 | ||||
| chr10:28532316-28532896 | Common:5; Rare:207 | ||||
| chr10:28533021-28533209 | Rare:77 | ||||
| chr10:28533610-28533929 | Common:4; Rare:145 | ||||
| chr10:28677245-28677526 | Common:5; Rare:130 |