| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8551843-8552075 | Common:1; Rare:45 | ||||
| chr17:8561198-8561221 | Rare:7 | ||||
| chr17:8580932-8581057 | Rare:23 | ||||
| chr17:8587127-8587440 | Common:1; Rare:76 | ||||
| chr17:8587514-8587816 | Common:1; Rare:50 | ||||
| chr17:8587870-8587958 | Common:1; Rare:19 | ||||
| chr17:8588618-8588665 | Common:1; Rare:7 | ||||
| chr17:8588890-8589049 | Common:1; Rare:27 | ||||
| chr17:8629704-8629802 | Rare:22 | ||||
| chr17:8631292-8631421 | Rare:40 | ||||
| chr17:9299696-9299708 | Rare:2 | ||||
| chr17:9305444-9305729 | Common:2; Rare:51 | ||||
| chr17:9345673-9345753 | Common:1; Rare:9 | ||||
| chr17:9353956-9354279 | Common:1; Rare:55 | ||||
| chr17:10695738-10696064 | Common:3; Rare:72; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 |