| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7262405-7262705 | Common:2; Rare:68 | ||||
| chr17:7307311-7307750 | Common:6; Rare:122 | ||||
| chr17:7313379-7313605 | Common:1; Rare:94 | ||||
| chr17:7315031-7315428 | Common:4; Rare:139 | ||||
| chr17:7350227-7350376 | Common:2; Rare:51 | ||||
| chr17:7350907-7351202 | Common:1; Rare:62 | ||||
| chr17:7351581-7351738 | Rare:29 | ||||
| chr17:7352037-7352224 | Rare:66 | ||||
| chr17:7403736-7403997 | Common:6; Rare:77 | ||||
| chr17:7404071-7404141 | Rare:38 | ||||
| chr17:7438144-7438366 | Common:1; Rare:47 | ||||
| chr17:7455742-7455863 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7479479-7479720 | Common:1; Rare:41 | ||||
| chr17:7483911-7484033 | Common:3; Rare:27 | ||||
| chr17:7484194-7484376 | Common:1; Rare:75 |