| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40822382-40822430 | Rare:18; Clinvar:1 | ||||
| chr17:40822567-40822643 | Rare:21 | ||||
| chr17:41505596-41505908 | Common:1; Rare:54 | ||||
| chr17:41524378-41524775 | Common:3; Rare:92; Clinvar:1 | ||||
| chr17:41624530-41624744 | Common:4; Rare:56 | ||||
| chr17:41688781-41688901 | Rare:45 | ||||
| chr17:41689303-41689541 | Common:2; Rare:89 | ||||
| chr17:41812617-41813277 | Common:3; Rare:168; Clinvar:9 | ||||
| chr17:42017139-42017470 | Rare:112 | ||||
| chr17:42017479-42017506 | Common:1; Rare:8 | ||||
| chr17:42422952-42423283 | Common:1; Rare:107; Clinvar:3 | ||||
| chr17:42458735-42458945 | Common:3; Rare:79 | ||||
| chr17:42566994-42567122 | Common:3; Rare:39 | ||||
| chr17:42577651-42577869 | Common:1; Rare:109 | ||||
| chr17:42609333-42609740 | Common:8; Rare:170; Clinvar (benign):2 |