| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:29292612-29292704 | Common:1; Rare:25 | ||||
| chr17:29590504-29590605 | Rare:17 | ||||
| chr17:29591774-29591944 | Rare:41 | ||||
| chr17:29682233-29682315 | Rare:10 | ||||
| chr17:29706453-29706863 | Common:1; Rare:61 | ||||
| chr17:29707050-29707169 | Common:1; Rare:27 | ||||
| chr17:29714254-29714456 | Common:1; Rare:23 | ||||
| chr17:29722763-29722983 | Common:1; Rare:39 | ||||
| chr17:29760380-29760585 | Common:2; Rare:36 | ||||
| chr17:29931372-29931461 | Rare:13 | ||||
| chr17:30212733-30212975 | Rare:62; Clinvar (benign):1 | ||||
| chr17:30551071-30551247 | Common:1; Rare:39 | ||||
| chr17:30576185-30576484 | Common:3; Rare:86 | ||||
| chr17:30599644-30599684 | Rare:6 | ||||
| chr17:30600087-30600264 | Rare:32 |