| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4739542-4739650 | Rare:27 | ||||
| chr17:4771778-4771931 | Common:1; Rare:46 | ||||
| chr17:4807007-4807218 | Common:4; Rare:66 | ||||
| chr17:4833122-4833554 | Common:1; Rare:115 | ||||
| chr17:4833558-4833637 | Rare:14 | ||||
| chr17:4939892-4940024 | Rare:46 | ||||
| chr17:4940027-4940338 | Common:2; Rare:83 | ||||
| chr17:4947918-4948041 | Rare:34 | ||||
| chr17:4948942-4949183 | Common:2; Rare:82 | ||||
| chr17:4949857-4950165 | Common:1; Rare:69 | ||||
| chr17:4967725-4968190 | Common:2; Rare:162 | ||||
| chr17:4987051-4987225 | Common:1; Rare:45 | ||||
| chr17:4987625-4987760 | Common:1; Rare:53 | ||||
| chr17:4997900-4998154 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr17:5078410-5078573 | Common:3; Rare:41 |