| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39665226-39665412 | Common:1; Rare:54; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:39667766-39668005 | Common:1; Rare:41 | ||||
| chr17:39688010-39688132 | Rare:39 | ||||
| chr17:39699894-39700221 | Rare:82 | ||||
| chr17:39927499-39927755 | Common:2; Rare:79 | ||||
| chr17:39980483-39980918 | Common:2; Rare:98 | ||||
| chr17:40033101-40033382 | Common:1; Rare:84 | ||||
| chr17:40054368-40054525 | Rare:35 | ||||
| chr17:40062692-40063027 | Common:1; Rare:95 | ||||
| chr17:40121814-40121986 | Common:2; Rare:64 | ||||
| chr17:40140145-40140631 | Common:6; Rare:221 | ||||
| chr17:40287572-40287944 | Rare:106 | ||||
| chr17:40318088-40318283 | Common:1; Rare:43 | ||||
| chr17:40417830-40418177 | Rare:105 | ||||
| chr17:41528269-41528548 | Common:1; Rare:66; Clinvar:1 |