| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7352088-7352169 | Rare:25 | ||||
| chr17:7438173-7438525 | Rare:85 | ||||
| chr17:7440475-7440788 | Rare:59 | ||||
| chr17:7479517-7479740 | Common:1; Rare:39 | ||||
| chr17:7484214-7484371 | Common:1; Rare:62 | ||||
| chr17:7484689-7484834 | Rare:61 | ||||
| chr17:7561770-7561996 | Common:2; Rare:65 | ||||
| chr17:7577279-7577358 | Rare:25 | ||||
| chr17:7579432-7579686 | Common:1; Rare:80 | ||||
| chr17:7583510-7583865 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584073-7584122 | Rare:11 | ||||
| chr17:7686397-7686692 | Rare:73 | ||||
| chr17:7687462-7687625 | Rare:35 | ||||
| chr17:7857911-7858085 | Rare:60 | ||||
| chr17:7885221-7885334 | Rare:34 |