| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699514-15699797 | Common:3; Rare:76 | ||||
| chr17:15999600-16000011 | Common:3; Rare:181; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217118-16217227 | Rare:27 | ||||
| chr17:17507016-17507254 | Common:4; Rare:71 | ||||
| chr17:17591595-17591932 | Common:1; Rare:96 | ||||
| chr17:18314928-18315332 | Common:1; Rare:117 | ||||
| chr17:18780936-18781301 | Common:7; Rare:94 | ||||
| chr17:18856195-18856362 | Common:1; Rare:27 | ||||
| chr17:19377903-19378031 | Common:1; Rare:30 | ||||
| chr17:19378174-19378545 | Common:2; Rare:92 | ||||
| chr17:19648602-19648806 | Common:2; Rare:68 | ||||
| chr17:19977798-19977958 | Common:1; Rare:55 | ||||
| chr17:21214148-21214351 | Common:2; Rare:92 | ||||
| chr17:27293952-27294141 | Common:1; Rare:83 | ||||
| chr17:27577277-27577451 | Common:1; Rare:30 |