| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38073151-38073495 | Common:1; Rare:92 | ||||
| chr2:38073987-38074566 | Common:1; Rare:336; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr2:38075373-38076102 | Common:6; Rare:336; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:38076046-38076369 | Common:3; Rare:181 | ||||
| chr2:38076411-38076588 | Common:5; Rare:58 | ||||
| chr2:38376072-38376781 | Common:6; Rare:392 | ||||
| chr2:38376717-38376922 | Common:2; Rare:130 | ||||
| chr2:38377181-38377649 | Common:8; Rare:428 | ||||
| chr2:38601999-38602628 | Common:17; Rare:391 | ||||
| chr2:38602540-38602790 | Common:1; Rare:81 | ||||
| chr2:38602790-38603254 | Common:13; Rare:475 | ||||
| chr2:38666540-38666910 | Common:2; Rare:72 | ||||
| chr2:38751101-38751612 | Common:14; Rare:592 | ||||
| chr2:38778010-38778479 | Common:1; Rare:149 | ||||
| chr2:38875808-38876068 | Common:6; Rare:229 |