| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41812829-41813022 | Rare:50; Clinvar:2 | ||||
| chr17:41918917-41919316 | Common:2; Rare:146; Clinvar:1 | ||||
| chr17:41966606-41966837 | Common:1; Rare:83 | ||||
| chr17:42017390-42017482 | Rare:40 | ||||
| chr17:42423153-42423399 | Common:1; Rare:65; Clinvar:1 | ||||
| chr17:42458738-42458914 | Common:1; Rare:70 | ||||
| chr17:42577645-42577789 | Rare:70 | ||||
| chr17:42609333-42609730 | Common:8; Rare:164; Clinvar (benign):2 | ||||
| chr17:42833381-42833530 | Rare:56 | ||||
| chr17:42964442-42964534 | Rare:43 | ||||
| chr17:43125338-43125642 | Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170303-43170488 | Common:2; Rare:37 | ||||
| chr17:43171024-43171233 | Rare:62 | ||||
| chr17:43545617-43545778 | Common:1; Rare:46 | ||||
| chr17:43900611-43900751 | Rare:42 |