| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40096327-40096350 | Common:1; Rare:3 | ||||
| chr17:40099215-40099457 | Common:2; Rare:68 | ||||
| chr17:40108220-40108361 | Rare:28 | ||||
| chr17:40120711-40120902 | Rare:39 | ||||
| chr17:41503046-41503349 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):5 | ||||
| chr17:41503382-41503689 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:41758465-41758792 | Common:1; Rare:72; Clinvar:8; Clinvar (benign):2 | ||||
| chr17:41769123-41769419 | Common:1; Rare:93; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:42323582-42323667 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chr17:42333725-42334015 | Rare:60; Clinvar:1 | ||||
| chr17:42422625-42422975 | Rare:140; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr17:42575786-42575878 | Rare:15 | ||||
| chr17:42794725-42794746 | Rare:5 | ||||
| chr17:42878185-42878242 | Rare:9 | ||||
| chr17:43002750-43002846 | Common:1; Rare:34 |