| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:27293863-27294429 | Common:3; Rare:197 | ||||
| chr17:27294483-27294659 | Common:1; Rare:46 | ||||
| chr17:27294732-27295145 | Common:4; Rare:85 | ||||
| chr17:27456233-27456522 | Common:2; Rare:95 | ||||
| chr17:27893062-27893182 | Rare:24 | ||||
| chr17:27893190-27893457 | Common:2; Rare:94 | ||||
| chr17:28041647-28041890 | Common:2; Rare:71 | ||||
| chr17:28318840-28319240 | Common:3; Rare:136 | ||||
| chr17:28319307-28319325 | Rare:4 | ||||
| chr17:28319329-28319439 | Common:4; Rare:42 | ||||
| chr17:28335015-28335150 | Rare:29 | ||||
| chr17:28335358-28335846 | Common:1; Rare:116 | ||||
| chr17:28336148-28336510 | Common:2; Rare:66 | ||||
| chr17:28357173-28357782 | Common:13; Rare:249; Clinvar (pathogenic):2 | ||||
| chr17:28405175-28405326 | Rare:40; Clinvar:2; Clinvar (pathogenic):1 |