| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40480671-40480788 | Rare:30 | ||||
| chr17:40501216-40501679 | Common:6; Rare:79 | ||||
| chr17:40821957-40822709 | Common:3; Rare:216; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:40966910-40967248 | Common:2; Rare:65 | ||||
| chr17:41396934-41397168 | Rare:59 | ||||
| chr17:41397598-41397909 | Rare:50 | ||||
| chr17:41440957-41441267 | Common:1; Rare:65 | ||||
| chr17:41466986-41467044 | Rare:20 | ||||
| chr17:41467350-41467708 | Common:4; Rare:57 | ||||
| chr17:41481127-41481391 | Rare:49 | ||||
| chr17:41521825-41522008 | Common:1; Rare:20 | ||||
| chr17:41583730-41584430 | Common:5; Rare:176; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:41584817-41585066 | Common:2; Rare:72; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:41586286-41587207 | Common:11; Rare:295; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr17:41612236-41612412 | Rare:57; Clinvar (pathogenic):2 |