| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41059584-41059718 | Common:1; Rare:35 | ||||
| chr17:41060084-41060347 | Common:3; Rare:63 | ||||
| chr17:41521905-41522232 | Common:4; Rare:55 | ||||
| chr17:41528137-41528647 | Common:4; Rare:130; Clinvar:3 | ||||
| chr17:41688479-41689012 | Common:3; Rare:192 | ||||
| chr17:41689158-41689628 | Common:4; Rare:172 | ||||
| chr17:41689750-41689859 | Rare:28 | ||||
| chr17:41734601-41734939 | Common:6; Rare:103 | ||||
| chr17:41772280-41772493 | Common:1; Rare:29 | ||||
| chr17:41772726-41772923 | Common:2; Rare:28 | ||||
| chr17:41785204-41785417 | Common:1; Rare:45 | ||||
| chr17:41785908-41786312 | Common:2; Rare:82 | ||||
| chr17:41786354-41786459 | Common:1; Rare:14 | ||||
| chr17:41786616-41787169 | Common:3; Rare:129; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:41811606-41811849 | Rare:73 |