| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122353210-122353520 | Rare:63 | ||||
| chr3:122432428-122433189 | Common:1; Rare:177 | ||||
| chr3:122467101-122467400 | Common:5; Rare:107 | ||||
| chr3:122651195-122652586 | Common:23; Rare:442 | ||||
| chr3:122733030-122733260 | Common:7; Rare:51 | ||||
| chr3:123053090-123053520 | Common:2; Rare:82 | ||||
| chr3:123068428-123068748 | Common:2; Rare:65 | ||||
| chr3:123447937-123448337 | Common:2; Rare:210; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:123475208-123475901 | Common:10; Rare:244 | ||||
| chr3:123586083-123586367 | Rare:46 | ||||
| chr3:123597602-123597863 | Rare:46 | ||||
| chr3:123602432-123602759 | Common:2; Rare:80 | ||||
| chr3:123605089-123605489 | Common:6; Rare:83 | ||||
| chr3:123619090-123619562 | Common:2; Rare:83 | ||||
| chr3:123621800-123622280 | Common:12; Rare:240 |