| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12068710-12069027 | Common:2; Rare:118 | ||||
| chr10:12129457-12129726 | Rare:109 | ||||
| chr10:12195817-12196241 | Rare:115 | ||||
| chr10:13099949-13100279 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13300022-13300164 | Rare:54; Clinvar:1 | ||||
| chr10:13348006-13348312 | Rare:97 | ||||
| chr10:13707177-13707295 | Common:2; Rare:24 | ||||
| chr10:14838029-14838383 | Common:2; Rare:98 | ||||
| chr10:14878607-14878884 | Common:2; Rare:88 | ||||
| chr10:14954017-14954192 | Rare:63 | ||||
| chr10:16817322-16817744 | Common:5; Rare:151 | ||||
| chr10:17228600-17228675 | Common:1; Rare:24 | ||||
| chr10:17228906-17229026 | Common:3; Rare:29 | ||||
| chr10:17643894-17644286 | Common:2; Rare:116 | ||||
| chr10:17809161-17809385 | Rare:30 |