| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4555316-4555554 | Common:3; Rare:109 | ||||
| chr17:4673087-4673277 | Rare:56 | ||||
| chr17:4704088-4704287 | Rare:96 | ||||
| chr17:4797565-4797688 | Common:1; Rare:35 | ||||
| chr17:4806984-4807204 | Common:4; Rare:69 | ||||
| chr17:4833155-4833554 | Common:1; Rare:106 | ||||
| chr17:4896445-4896811 | Common:1; Rare:134 | ||||
| chr17:4939815-4940400 | Common:2; Rare:171 | ||||
| chr17:4942339-4942662 | Common:1; Rare:109 | ||||
| chr17:4948892-4949157 | Common:1; Rare:85 | ||||
| chr17:4949316-4949625 | Common:2; Rare:87 | ||||
| chr17:4955824-4956005 | Common:3; Rare:54 | ||||
| chr17:4967721-4968276 | Common:3; Rare:179 | ||||
| chr17:4987417-4987753 | Common:3; Rare:110 | ||||
| chr17:4998037-4998140 | Common:1; Rare:43; Clinvar (benign):1 |