| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21214593-21214772 | Common:1; Rare:47 | ||||
| chr17:21253270-21253568 | Common:5; Rare:94 | ||||
| chr17:27293903-27294398 | Common:3; Rare:179 | ||||
| chr17:27294409-27294479 | Common:1; Rare:16 | ||||
| chr17:28318942-28319329 | Common:3; Rare:138 | ||||
| chr17:28335381-28335850 | Common:1; Rare:112 | ||||
| chr17:28357455-28357667 | Common:5; Rare:105 | ||||
| chr17:28552569-28552757 | Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571497-28571721 | Rare:56 | ||||
| chr17:28576858-28577061 | Common:2; Rare:53 | ||||
| chr17:28598903-28599153 | Common:3; Rare:80 | ||||
| chr17:28645094-28645323 | Common:1; Rare:84 | ||||
| chr17:28661881-28661970 | Rare:37 | ||||
| chr17:28662122-28662314 | Rare:77 | ||||
| chr17:28711297-28711547 | Common:3; Rare:71 |