| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19534376-19534422 | Rare:16 | ||||
| chr17:19648609-19649131 | Common:3; Rare:190; Clinvar (benign):1 | ||||
| chr17:19977798-19977963 | Common:1; Rare:57 | ||||
| chr17:20010265-20010562 | Common:1; Rare:43 | ||||
| chr17:21214140-21214354 | Common:2; Rare:96 | ||||
| chr17:27294011-27294140 | Common:1; Rare:52 | ||||
| chr17:27294273-27294380 | Common:1; Rare:33 | ||||
| chr17:28041617-28041764 | Common:1; Rare:35 | ||||
| chr17:28318890-28319359 | Common:3; Rare:167 | ||||
| chr17:28335376-28335841 | Common:1; Rare:112 | ||||
| chr17:28357407-28357679 | Common:6; Rare:135 | ||||
| chr17:28368206-28368513 | Common:1; Rare:59 | ||||
| chr17:28368519-28369430 | Common:3; Rare:273 | ||||
| chr17:28370138-28370505 | Common:2; Rare:73 | ||||
| chr17:28405719-28405838 | Rare:26 |