| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12129472-12129719 | Rare:104 | ||||
| chr10:12195817-12196238 | Rare:112 | ||||
| chr10:13099949-13100273 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13300055-13300090 | Rare:13; Clinvar:1 | ||||
| chr10:13348008-13348351 | Rare:112 | ||||
| chr10:14838029-14838341 | Common:2; Rare:81 | ||||
| chr10:14878637-14878884 | Common:2; Rare:73 | ||||
| chr10:14954023-14954195 | Rare:61 | ||||
| chr10:15097331-15097401 | Common:1; Rare:31 | ||||
| chr10:15860440-15860530 | Rare:24 | ||||
| chr10:16817328-16817744 | Common:5; Rare:149 | ||||
| chr10:17229114-17229310 | Common:1; Rare:37 | ||||
| chr10:17643898-17644279 | Common:2; Rare:113 | ||||
| chr10:18651548-18651748 | Common:1; Rare:85 | ||||
| chr10:18659254-18659419 | Common:2; Rare:53 |