| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7404433-7404661 | Common:2; Rare:65 | ||||
| chr17:7438183-7438317 | Rare:31 | ||||
| chr17:7440467-7440831 | Rare:75 | ||||
| chr17:7455765-7455830 | Rare:28; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7479557-7479775 | Common:1; Rare:34 | ||||
| chr17:7483906-7484002 | Common:2; Rare:22 | ||||
| chr17:7484219-7484371 | Common:1; Rare:62 | ||||
| chr17:7484690-7484834 | Rare:60 | ||||
| chr17:7561735-7562017 | Common:2; Rare:87 | ||||
| chr17:7583689-7583874 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584045-7584141 | Rare:27 | ||||
| chr17:7627482-7627508 | Common:1; Rare:5 | ||||
| chr17:7627709-7628021 | Common:3; Rare:105 | ||||
| chr17:7686073-7686735 | Rare:181 | ||||
| chr17:7687439-7687569 | Rare:33; Clinvar:2 |