| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4731150-4731540 | Common:8; Rare:252 | ||||
| chr17:4731555-4731955 | Common:7; Rare:338 | ||||
| chr17:4736183-4736593 | Common:5; Rare:185 | ||||
| chr17:4795877-4797695 | Common:26; Rare:968 | ||||
| chr17:4806900-4807260 | Common:19; Rare:386 | ||||
| chr17:4833085-4833546 | Common:4; Rare:584 | ||||
| chr17:4833617-4834492 | Common:6; Rare:256 | ||||
| chr17:4939888-4940671 | Common:19; Rare:987 | ||||
| chr17:4947249-4947649 | Common:6; Rare:210 | ||||
| chr17:4947770-4948850 | Common:27; Rare:1263 | ||||
| chr17:4948923-4949280 | Common:8; Rare:404 | ||||
| chr17:4949310-4949762 | Common:8; Rare:271 | ||||
| chr17:4949767-4950219 | Common:5; Rare:432 | ||||
| chr17:4950296-4950860 | Common:3; Rare:429 | ||||
| chr17:4950820-4951553 | Common:5; Rare:272; Clinvar (benign):5 |