| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415136-80415189 | Common:1; Rare:36 | ||||
| chr17:81239031-81239317 | Common:2; Rare:95 | ||||
| chr17:81666268-81666387 | Rare:30 | ||||
| chr17:81666544-81666763 | Common:1; Rare:98 | ||||
| chr17:81683713-81684057 | Common:4; Rare:171 | ||||
| chr17:81703286-81703510 | Common:2; Rare:62; Clinvar (benign):2 | ||||
| chr17:81833243-81833339 | Rare:41 | ||||
| chr17:81891412-81891805 | Common:3; Rare:158 | ||||
| chr17:81937228-81937451 | Rare:86 | ||||
| chr17:81977433-81977642 | Rare:75 | ||||
| chr17:82037672-82037872 | Common:1; Rare:79 | ||||
| chr17:82051598-82051931 | Common:2; Rare:102 | ||||
| chr17:82228382-82228461 | Rare:18 | ||||
| chr17:82273357-82273822 | Common:2; Rare:166 |