| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:27293954-27294149 | Common:2; Rare:89 | ||||
| chr17:27294287-27294380 | Common:1; Rare:29 | ||||
| chr17:28042250-28042633 | Common:2; Rare:85 | ||||
| chr17:28042986-28043034 | Rare:16 | ||||
| chr17:28318932-28319292 | Common:3; Rare:129 | ||||
| chr17:28335350-28335850 | Common:1; Rare:117 | ||||
| chr17:28357373-28357699 | Common:6; Rare:154; Clinvar (pathogenic):1 | ||||
| chr17:28371419-28371746 | Common:5; Rare:57 | ||||
| chr17:28406134-28406268 | Rare:24; Clinvar:1 | ||||
| chr17:28571481-28571667 | Rare:49 | ||||
| chr17:28576861-28577054 | Common:2; Rare:53 | ||||
| chr17:28598994-28599165 | Common:2; Rare:47 | ||||
| chr17:28645013-28645289 | Common:1; Rare:118 | ||||
| chr17:28661854-28661975 | Rare:49 | ||||
| chr17:28662109-28662325 | Rare:89 |