| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7561803-7562008 | Common:2; Rare:55 | ||||
| chr17:7578136-7578459 | Rare:90 | ||||
| chr17:7579206-7579561 | Common:1; Rare:127 | ||||
| chr17:7579565-7579762 | Rare:67 | ||||
| chr17:7580138-7580585 | Common:1; Rare:132 | ||||
| chr17:7580694-7581060 | Common:1; Rare:114 | ||||
| chr17:7583508-7583865 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584068-7584327 | Common:1; Rare:58 | ||||
| chr17:7627787-7627969 | Common:2; Rare:58 | ||||
| chr17:7686402-7686677 | Rare:69 | ||||
| chr17:7717628-7717787 | Rare:34 | ||||
| chr17:7843644-7843741 | Rare:32 | ||||
| chr17:7843864-7844210 | Common:4; Rare:100 | ||||
| chr17:7857100-7857371 | Common:1; Rare:133 | ||||
| chr17:7857372-7857735 | Common:3; Rare:116 |