| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76726491-76726876 | Common:5; Rare:139 | ||||
| chr17:76737318-76737687 | Common:4; Rare:129 | ||||
| chr17:76737870-76738129 | Common:4; Rare:75 | ||||
| chr17:77287759-77288015 | Rare:34 | ||||
| chr17:77451240-77451520 | Common:1; Rare:66 | ||||
| chr17:77453601-77453825 | Common:3; Rare:42 | ||||
| chr17:77454307-77454425 | Common:2; Rare:20 | ||||
| chr17:78130470-78130822 | Common:2; Rare:69 | ||||
| chr17:78146194-78146434 | Common:2; Rare:52 | ||||
| chr17:78187040-78187391 | Common:3; Rare:116 | ||||
| chr17:78378530-78378680 | Rare:49 | ||||
| chr17:78782203-78782577 | Common:9; Rare:122 | ||||
| chr17:78840745-78841099 | Common:2; Rare:134 | ||||
| chr17:79009707-79009930 | Common:9; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:80035830-80036019 | Common:1; Rare:63 |