| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35119793-35120018 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:35142048-35142108 | Rare:20 | ||||
| chr17:35242212-35242711 | Common:2; Rare:92 | ||||
| chr17:35242892-35243355 | Rare:126 | ||||
| chr17:35432472-35432768 | Common:1; Rare:47 | ||||
| chr17:35432849-35432962 | Rare:17 | ||||
| chr17:35433148-35433494 | Common:4; Rare:77 | ||||
| chr17:35433627-35433822 | Common:1; Rare:38 | ||||
| chr17:35448253-35448434 | Rare:43 | ||||
| chr17:35487826-35487874 | Rare:18 | ||||
| chr17:35487882-35487906 | Rare:2 | ||||
| chr17:35577920-35577997 | Common:1; Rare:24; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr17:35578330-35578851 | Common:3; Rare:118; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:35578860-35578951 | Rare:14 | ||||
| chr17:35579220-35579259 | Rare:5 |