| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80147089-80147334 | Common:5; Rare:95 | ||||
| chr17:80220309-80220469 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415109-80415195 | Common:1; Rare:57 | ||||
| chr17:80991804-80991928 | Common:1; Rare:50 | ||||
| chr17:81082809-81083005 | Rare:41 | ||||
| chr17:81083214-81083564 | Common:1; Rare:101 | ||||
| chr17:81239017-81239321 | Common:2; Rare:104 | ||||
| chr17:81295182-81295378 | Common:1; Rare:42 | ||||
| chr17:81512118-81512376 | Common:1; Rare:131; Clinvar:3; Clinvar (benign):15 | ||||
| chr17:81512715-81513060 | Common:7; Rare:191; Clinvar (benign):14 | ||||
| chr17:81552331-81552457 | Common:1; Rare:50 | ||||
| chr17:81666558-81666779 | Common:1; Rare:100 | ||||
| chr17:81683716-81684060 | Common:4; Rare:171 | ||||
| chr17:81703277-81703551 | Common:2; Rare:84; Clinvar (benign):2 | ||||
| chr17:81803814-81804176 | Common:1; Rare:79 |