| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:20155827-20156121 | Common:2; Rare:180 | ||||
| chr17:21042180-21042600 | Common:7; Rare:236 | ||||
| chr17:21042901-21043420 | Common:13; Rare:356 | ||||
| chr17:21126502-21127140 | Common:7; Rare:278 | ||||
| chr17:21214128-21214404 | Common:4; Rare:240 | ||||
| chr17:21214520-21214740 | Common:3; Rare:108 | ||||
| chr17:21253406-21253581 | Common:9; Rare:104 | ||||
| chr17:21284419-21284725 | Common:2; Rare:142 | ||||
| chr17:27293917-27294149 | Common:3; Rare:185 | ||||
| chr17:27294170-27294380 | Common:1; Rare:63 | ||||
| chr17:27456235-27456476 | Common:2; Rare:142 | ||||
| chr17:27893330-27893472 | Rare:50 | ||||
| chr17:28318890-28319285 | Common:6; Rare:261 | ||||
| chr17:28335385-28335857 | Common:2; Rare:209 | ||||
| chr17:28357448-28357805 | Common:11; Rare:295; Clinvar (pathogenic):3 |