| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143445169-143445387 | Rare:36 | ||||
| chr3:146542344-146542530 | Rare:27 | ||||
| chr3:149145444-149145653 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:152205418-152205652 | Common:2; Rare:23 | ||||
| chr3:153164015-153164079 | Common:1; Rare:14 | ||||
| chr3:153164496-153164530 | Rare:4 | ||||
| chr3:156816979-156817330 | Rare:105 | ||||
| chr3:157156496-157156772 | Common:2; Rare:52 | ||||
| chr3:157174861-157175147 | Common:3; Rare:126 | ||||
| chr3:160515219-160515481 | Common:1; Rare:52 | ||||
| chr3:169952127-169952325 | Common:2; Rare:30 | ||||
| chr3:169971324-169971635 | Common:5; Rare:52 | ||||
| chr3:172130584-172130765 | Common:1; Rare:30 | ||||
| chr3:172131554-172131598 | Rare:9 | ||||
| chr3:185922671-185922775 | Rare:22 |