| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80035843-80036004 | Common:1; Rare:58 | ||||
| chr17:80147095-80147331 | Common:5; Rare:92 | ||||
| chr17:80220309-80220478 | Common:1; Rare:64; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415105-80415197 | Common:1; Rare:64 | ||||
| chr17:80415420-80415523 | Common:4; Rare:42 | ||||
| chr17:80991804-80991933 | Common:1; Rare:52 | ||||
| chr17:81239036-81239317 | Common:2; Rare:92 | ||||
| chr17:81295266-81295389 | Common:1; Rare:26 | ||||
| chr17:81512118-81512372 | Common:1; Rare:125; Clinvar:3; Clinvar (benign):14 | ||||
| chr17:81666540-81666763 | Common:1; Rare:99 | ||||
| chr17:81683663-81684052 | Common:4; Rare:198 | ||||
| chr17:81703286-81703504 | Common:2; Rare:61; Clinvar (benign):2 | ||||
| chr17:81833243-81833351 | Rare:45 | ||||
| chr17:81860911-81861123 | Common:1; Rare:64 | ||||
| chr17:81871298-81871425 | Rare:41 |