| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28357427-28357715 | Common:5; Rare:144; Clinvar (pathogenic):1 | ||||
| chr17:28571497-28571662 | Rare:39 | ||||
| chr17:28598886-28599170 | Common:3; Rare:91 | ||||
| chr17:28645082-28645325 | Common:1; Rare:93 | ||||
| chr17:28661877-28661956 | Rare:35 | ||||
| chr17:28662105-28662319 | Rare:87 | ||||
| chr17:28717858-28718002 | Rare:30 | ||||
| chr17:28718136-28718324 | Rare:53 | ||||
| chr17:28719655-28720066 | Common:1; Rare:121 | ||||
| chr17:28728726-28728811 | Rare:32 | ||||
| chr17:28812359-28812620 | Common:1; Rare:68 | ||||
| chr17:28842727-28842863 | Rare:51 | ||||
| chr17:28854961-28855047 | Rare:25 | ||||
| chr17:28897617-28897732 | Common:1; Rare:38 | ||||
| chr17:29180339-29180519 | Common:1; Rare:38 |