| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46181872-46182506 | Common:3; Rare:108 | ||||
| chr13:46182644-46182802 | Rare:21 | ||||
| chr13:46211757-46212015 | Common:2; Rare:76 | ||||
| chr13:46387194-46387434 | Rare:65 | ||||
| chr13:46390139-46390184 | Rare:7 | ||||
| chr13:46552967-46553428 | Common:4; Rare:141 | ||||
| chr13:46679491-46679814 | Common:1; Rare:66 | ||||
| chr13:46679913-46680148 | Common:1; Rare:33 | ||||
| chr13:46796505-46796758 | Common:2; Rare:67 | ||||
| chr13:46796923-46796975 | Rare:15 | ||||
| chr13:46797040-46797440 | Common:4; Rare:113 | ||||
| chr13:48001198-48001485 | Common:3; Rare:131; Clinvar:5; Clinvar (benign):8 | ||||
| chr13:48037357-48038233 | Common:11; Rare:309; Clinvar:2 | ||||
| chr13:48094986-48095272 | Common:2; Rare:137 | ||||
| chr13:48233052-48233289 | Common:1; Rare:81 |