| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152205410-152205569 | Common:1; Rare:17 | ||||
| chr3:152338405-152338551 | Rare:28 | ||||
| chr3:152349876-152350120 | Common:1; Rare:45 | ||||
| chr3:153162837-153162994 | Rare:27 | ||||
| chr3:154972040-154972249 | Rare:27 | ||||
| chr3:156816968-156817090 | Rare:48 | ||||
| chr3:157174866-157175322 | Common:3; Rare:195 | ||||
| chr3:169764853-169765181 | Common:1; Rare:124; Clinvar:17; Clinvar (pathogenic):6 | ||||
| chr3:172514966-172515264 | Common:1; Rare:59 | ||||
| chr3:179180426-179180565 | Common:1; Rare:13 | ||||
| chr3:179229059-179229402 | Rare:53; Clinvar (benign):1 | ||||
| chr3:179410826-179410889 | Rare:15 | ||||
| chr3:180615191-180615317 | Common:1; Rare:19 | ||||
| chr3:182912524-182912602 | Rare:18 | ||||
| chr3:183107949-183108152 | Common:2; Rare:38 |