| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33798985-33799245 | Rare:79 | ||||
| chr3:36993056-36993586 | Common:2; Rare:187; Clinvar:34; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr3:36993663-36993830 | Rare:68; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:37176255-37176381 | Rare:38 | ||||
| chr3:37243146-37243365 | Common:1; Rare:59 | ||||
| chr3:37998996-37999346 | Common:5; Rare:109 | ||||
| chr3:38138607-38138701 | Common:2; Rare:40; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:38165443-38165510 | Rare:18 | ||||
| chr3:38165770-38165883 | Rare:44 | ||||
| chr3:38346714-38346881 | Rare:52 | ||||
| chr3:38496045-38496373 | Common:2; Rare:100 | ||||
| chr3:38496697-38496960 | Rare:55 | ||||
| chr3:39051943-39052073 | Common:1; Rare:50 | ||||
| chr3:39107558-39107680 | Common:2; Rare:40 | ||||
| chr3:39153554-39153843 | Common:5; Rare:91 |