| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146160977-146161386 | Common:2; Rare:124; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146251022-146251364 | Common:2; Rare:90 | ||||
| chr3:146544484-146544834 | Common:5; Rare:82 | ||||
| chr3:146544855-146544942 | Rare:25 | ||||
| chr3:148991350-148991636 | Common:5; Rare:123; Clinvar (benign):1 | ||||
| chr3:149129549-149129692 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149166925-149167134 | Rare:41; Clinvar:1 | ||||
| chr3:149377509-149377937 | Common:1; Rare:97 | ||||
| chr3:149657971-149658175 | Rare:44 | ||||
| chr3:149752434-149752596 | Common:2; Rare:54 | ||||
| chr3:149812572-149812740 | Common:1; Rare:46 | ||||
| chr3:149813117-149813260 | Common:1; Rare:50 | ||||
| chr3:150603157-150603435 | Common:2; Rare:115 | ||||
| chr3:150703703-150704025 | Common:3; Rare:163 | ||||
| chr3:152268687-152268978 | Rare:113 |