| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28335342-28335851 | Common:1; Rare:121 | ||||
| chr17:28357291-28357691 | Common:11; Rare:181; Clinvar (pathogenic):1 | ||||
| chr17:28371927-28372091 | Rare:41 | ||||
| chr17:28372453-28372738 | Rare:65 | ||||
| chr17:28552339-28552381 | Rare:14 | ||||
| chr17:28598975-28599153 | Common:2; Rare:58 | ||||
| chr17:28661728-28661967 | Common:1; Rare:100 | ||||
| chr17:28662052-28662330 | Common:1; Rare:97 | ||||
| chr17:28673266-28673510 | Common:1; Rare:54 | ||||
| chr17:28719655-28720029 | Common:1; Rare:102 | ||||
| chr17:28722876-28722917 | Rare:12 | ||||
| chr17:28726905-28727192 | Common:2; Rare:59 | ||||
| chr17:28743889-28744025 | Common:4; Rare:35 | ||||
| chr17:28842731-28842865 | Rare:49 | ||||
| chr17:28854961-28855068 | Rare:40 |