| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:2331189-2331398 | Rare:43 | ||||
| chr2:3282586-3282690 | Rare:27 | ||||
| chr2:3377774-3377953 | Rare:52 | ||||
| chr2:3379600-3379808 | Common:2; Rare:82 | ||||
| chr2:3519492-3519587 | Common:2; Rare:38 | ||||
| chr2:3558252-3558571 | Common:6; Rare:122 | ||||
| chr2:3575069-3575358 | Common:3; Rare:82; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:6866480-6866654 | Common:1; Rare:32 | ||||
| chr2:6932960-6933104 | Common:1; Rare:32 | ||||
| chr2:8837327-8837648 | Common:3; Rare:84 | ||||
| chr2:9003955-9004084 | Rare:54 | ||||
| chr2:9423371-9423728 | Rare:108 | ||||
| chr2:9473650-9473840 | Rare:53 | ||||
| chr2:9474491-9474642 | Common:6; Rare:71 | ||||
| chr2:9555609-9555926 | Common:2; Rare:104 |