| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636226-3636546 | Common:5; Rare:95; Clinvar (benign):2 | ||||
| chr17:3668552-3668861 | Common:2; Rare:126 | ||||
| chr17:3723762-3723925 | Common:1; Rare:91 | ||||
| chr17:4143010-4143258 | Rare:80 | ||||
| chr17:4143597-4143740 | Common:4; Rare:80 | ||||
| chr17:4263943-4264072 | Rare:52 | ||||
| chr17:4555304-4555503 | Common:3; Rare:92 | ||||
| chr17:4704110-4704231 | Rare:69 | ||||
| chr17:4731274-4731498 | Common:2; Rare:71 | ||||
| chr17:4736348-4736496 | Rare:31 | ||||
| chr17:4739388-4739530 | Common:4; Rare:32 | ||||
| chr17:4739542-4739630 | Rare:25 | ||||
| chr17:4771778-4771962 | Common:1; Rare:54 | ||||
| chr17:4786358-4786492 | Rare:33 | ||||
| chr17:4788722-4789117 | Rare:100 |