| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80147069-80147374 | Common:7; Rare:123 | ||||
| chr17:80220297-80220459 | Common:1; Rare:65; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415090-80415189 | Common:1; Rare:64 | ||||
| chr17:80415377-80415492 | Common:4; Rare:45 | ||||
| chr17:80544784-80544905 | Rare:26 | ||||
| chr17:80991804-80991960 | Common:1; Rare:62 | ||||
| chr17:81239048-81239317 | Common:2; Rare:89 | ||||
| chr17:81295278-81295442 | Common:2; Rare:41 | ||||
| chr17:81552322-81552479 | Common:1; Rare:61 | ||||
| chr17:81636922-81637246 | Common:3; Rare:128 | ||||
| chr17:81666268-81666352 | Rare:22 | ||||
| chr17:81666524-81666785 | Common:1; Rare:117 | ||||
| chr17:81683641-81684069 | Common:5; Rare:227 | ||||
| chr17:81703294-81703531 | Common:2; Rare:70; Clinvar (benign):2 | ||||
| chr17:81833243-81833385 | Rare:63 |