| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001450-143001631 | Common:2; Rare:65 | ||||
| chr3:143971754-143971825 | Common:1; Rare:32 | ||||
| chr3:149129549-149129676 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:150408095-150408320 | Common:2; Rare:78 | ||||
| chr3:150603168-150603347 | Common:2; Rare:69 | ||||
| chr3:151316803-151316945 | Common:1; Rare:26 | ||||
| chr3:152268585-152269147 | Common:2; Rare:206 | ||||
| chr3:152269280-152269332 | Rare:16 | ||||
| chr3:152269477-152269759 | Common:2; Rare:91 | ||||
| chr3:154121264-154121451 | Common:2; Rare:80 | ||||
| chr3:154324413-154324666 | Rare:85 | ||||
| chr3:155079823-155080206 | Common:1; Rare:88 | ||||
| chr3:155080228-155080403 | Common:1; Rare:46 | ||||
| chr3:156674377-156674624 | Common:3; Rare:69 | ||||
| chr3:157160072-157160334 | Rare:107 |