| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2337378-2337501 | Rare:36 | ||||
| chr17:2393802-2394039 | Common:3; Rare:97 | ||||
| chr17:2394051-2394263 | Common:1; Rare:81 | ||||
| chr17:2396716-2397032 | Common:2; Rare:66 | ||||
| chr17:2400961-2401114 | Rare:35 | ||||
| chr17:2511801-2512017 | Common:2; Rare:68 | ||||
| chr17:2711746-2712031 | Common:2; Rare:80 | ||||
| chr17:3636232-3636468 | Common:4; Rare:68; Clinvar (benign):1 | ||||
| chr17:3668463-3668838 | Common:3; Rare:155 | ||||
| chr17:3723705-3723964 | Common:1; Rare:143 | ||||
| chr17:3892955-3893259 | Common:3; Rare:102 | ||||
| chr17:4142913-4143234 | Common:3; Rare:118 | ||||
| chr17:4143597-4143777 | Common:5; Rare:108 | ||||
| chr17:4263934-4264096 | Rare:65 | ||||
| chr17:4366583-4366906 | Common:1; Rare:126 |