| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21551515-21551708 | Common:2; Rare:49 | ||||
| chr17:27293894-27294243 | Common:2; Rare:131 | ||||
| chr17:27294309-27294881 | Common:5; Rare:142 | ||||
| chr17:27456261-27456486 | Common:1; Rare:72 | ||||
| chr17:27559668-27559919 | Common:2; Rare:51 | ||||
| chr17:27560023-27560378 | Common:2; Rare:71 | ||||
| chr17:27893281-27893452 | Common:1; Rare:69 | ||||
| chr17:28041650-28041856 | Common:2; Rare:63 | ||||
| chr17:28318837-28319261 | Common:3; Rare:151 | ||||
| chr17:28319295-28319404 | Rare:39 | ||||
| chr17:28319511-28319616 | Rare:21 | ||||
| chr17:28335351-28335846 | Common:1; Rare:117 | ||||
| chr17:28336132-28336529 | Common:2; Rare:75 | ||||
| chr17:28357390-28357782 | Common:7; Rare:180; Clinvar (pathogenic):2 | ||||
| chr17:28371343-28371802 | Common:6; Rare:85 |