| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:7818364-7818526 | Common:1; Rare:39 | ||||
| chr10:12068753-12069018 | Common:2; Rare:101 | ||||
| chr10:12195814-12196241 | Rare:115 | ||||
| chr10:13099949-13100234 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:13300043-13300166 | Rare:46; Clinvar:1 | ||||
| chr10:14838023-14838393 | Common:2; Rare:106 | ||||
| chr10:14878606-14878882 | Common:2; Rare:88 | ||||
| chr10:14954062-14954194 | Rare:36 | ||||
| chr10:15097317-15097378 | Common:1; Rare:26 | ||||
| chr10:15860499-15860586 | Rare:22 | ||||
| chr10:16436784-16437021 | Common:2; Rare:52 | ||||
| chr10:17229119-17229310 | Common:1; Rare:36 | ||||
| chr10:17643894-17644241 | Common:2; Rare:103 | ||||
| chr10:18651543-18651787 | Common:1; Rare:98 | ||||
| chr10:18659101-18659405 | Common:3; Rare:91 |