| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79009663-79009917 | Common:9; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:79024149-79024270 | Common:1; Rare:22 | ||||
| chr17:80035824-80036062 | Common:1; Rare:77 | ||||
| chr17:80036479-80036674 | Common:2; Rare:48; Clinvar (benign):2 | ||||
| chr17:80147101-80147354 | Common:5; Rare:99 | ||||
| chr17:80220309-80220495 | Common:1; Rare:66; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80337547-80337980 | Common:2; Rare:108 | ||||
| chr17:80372597-80373165 | Common:3; Rare:195; Clinvar:2 | ||||
| chr17:80376114-80376441 | Common:5; Rare:94; Clinvar:1 | ||||
| chr17:80385288-80385594 | Common:1; Rare:87 | ||||
| chr17:80388370-80388617 | Common:5; Rare:70 | ||||
| chr17:80415069-80415540 | Common:5; Rare:234 | ||||
| chr17:80991804-80991938 | Common:1; Rare:54 | ||||
| chr17:81034872-81035190 | Common:3; Rare:133 | ||||
| chr17:81087218-81087511 | Common:2; Rare:81 |