| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40100717-40100964 | Common:3; Rare:51 | ||||
| chr17:40121838-40121989 | Common:2; Rare:59 | ||||
| chr17:40140145-40140682 | Common:6; Rare:243 | ||||
| chr17:40140710-40140787 | Rare:34 | ||||
| chr17:40176876-40177113 | Common:1; Rare:41 | ||||
| chr17:40177396-40177626 | Common:1; Rare:77 | ||||
| chr17:40219170-40219431 | Common:3; Rare:95 | ||||
| chr17:40342027-40342199 | Common:1; Rare:36 | ||||
| chr17:40703084-40703337 | Common:1; Rare:70 | ||||
| chr17:40822596-40822745 | Rare:31 | ||||
| chr17:41501870-41502636 | Common:1; Rare:186; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:41503966-41504665 | Common:3; Rare:128 | ||||
| chr17:41505806-41505898 | Rare:13 | ||||
| chr17:41523950-41524550 | Common:5; Rare:201; Clinvar:1 | ||||
| chr17:41527826-41528399 | Common:4; Rare:191; Clinvar:4 |