| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19648626-19648888 | Common:3; Rare:89 | ||||
| chr17:19977789-19977945 | Common:1; Rare:53 | ||||
| chr17:21183442-21183738 | Rare:65 | ||||
| chr17:21214140-21214375 | Common:2; Rare:109 | ||||
| chr17:21214571-21214658 | Common:1; Rare:33 | ||||
| chr17:27293992-27294195 | Common:2; Rare:82 | ||||
| chr17:27294310-27294402 | Common:1; Rare:29 | ||||
| chr17:27294408-27294670 | Common:2; Rare:68 | ||||
| chr17:28042255-28042276 | Rare:7 | ||||
| chr17:28042990-28043104 | Rare:42 | ||||
| chr17:28335376-28335846 | Common:1; Rare:113 | ||||
| chr17:28357318-28357699 | Common:11; Rare:175; Clinvar (pathogenic):1 | ||||
| chr17:28384555-28384854 | Rare:89 | ||||
| chr17:28387959-28388109 | Rare:27 | ||||
| chr17:28405679-28405865 | Rare:43 |