| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21042201-21042456 | Common:1; Rare:95 | ||||
| chr17:21042894-21043362 | Common:6; Rare:174 | ||||
| chr17:21043381-21043448 | Rare:27 | ||||
| chr17:21214086-21214395 | Common:2; Rare:142 | ||||
| chr17:27293916-27294149 | Common:2; Rare:102 | ||||
| chr17:27294182-27294428 | Common:1; Rare:73 | ||||
| chr17:27456252-27456480 | Common:1; Rare:75 | ||||
| chr17:28318918-28319257 | Common:3; Rare:120 | ||||
| chr17:28319276-28319348 | Rare:25 | ||||
| chr17:28335347-28335835 | Common:1; Rare:116 | ||||
| chr17:28357451-28357767 | Common:5; Rare:154; Clinvar (pathogenic):2 | ||||
| chr17:28371872-28372070 | Rare:43 | ||||
| chr17:28405580-28405866 | Common:1; Rare:73 | ||||
| chr17:28406170-28406268 | Rare:17; Clinvar:1 | ||||
| chr17:28571489-28571653 | Rare:44 |