| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21214086-21214375 | Common:2; Rare:136 | ||||
| chr17:21214551-21214761 | Common:1; Rare:66 | ||||
| chr17:27293929-27294143 | Common:1; Rare:90 | ||||
| chr17:28041474-28041775 | Common:1; Rare:75 | ||||
| chr17:28042250-28042543 | Common:2; Rare:73 | ||||
| chr17:28318932-28319235 | Common:3; Rare:102 | ||||
| chr17:28319276-28319335 | Rare:18 | ||||
| chr17:28335342-28335824 | Common:1; Rare:116 | ||||
| chr17:28357288-28357804 | Common:12; Rare:221; Clinvar (pathogenic):2 | ||||
| chr17:28406164-28406263 | Rare:20; Clinvar:1 | ||||
| chr17:28571480-28571676 | Rare:50 | ||||
| chr17:28584184-28584722 | Common:3; Rare:140 | ||||
| chr17:28598952-28599115 | Common:1; Rare:55 | ||||
| chr17:28616390-28616698 | Common:1; Rare:83 | ||||
| chr17:28645068-28645306 | Common:1; Rare:94 |