| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28719489-28720066 | Common:1; Rare:164 | ||||
| chr17:28720193-28720296 | Common:2; Rare:54 | ||||
| chr17:28720549-28720661 | Rare:45 | ||||
| chr17:28725152-28725439 | Common:1; Rare:114 | ||||
| chr17:28726155-28726247 | Common:1; Rare:18 | ||||
| chr17:28727131-28727495 | Rare:73 | ||||
| chr17:28727917-28728300 | Common:1; Rare:85 | ||||
| chr17:28728527-28729124 | Common:2; Rare:169; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:28743429-28743605 | Rare:27 | ||||
| chr17:28743767-28744173 | Common:4; Rare:114 | ||||
| chr17:28744204-28744536 | Common:2; Rare:101 | ||||
| chr17:28812188-28812234 | Rare:10 | ||||
| chr17:28812385-28812832 | Common:3; Rare:110 | ||||
| chr17:28842694-28842980 | Common:2; Rare:96 | ||||
| chr17:28854567-28855258 | Common:2; Rare:176 |