| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40471328-40471728 | Common:1; Rare:120 | ||||
| chr17:40542704-40542932 | Common:1; Rare:46 | ||||
| chr17:41544573-41544686 | Rare:22 | ||||
| chr17:41548834-41549936 | Common:14; Rare:259 | ||||
| chr17:41666432-41667147 | Common:6; Rare:195 | ||||
| chr17:41775590-41775728 | Common:1; Rare:32 | ||||
| chr17:42050548-42050655 | Rare:15 | ||||
| chr17:42050817-42051217 | Common:1; Rare:84 | ||||
| chr17:42153924-42154324 | Common:3; Rare:113 | ||||
| chr17:42184151-42184362 | Common:1; Rare:71 | ||||
| chr17:42200835-42200942 | Common:1; Rare:24 | ||||
| chr17:42201090-42201400 | Rare:55 | ||||
| chr17:42275482-42275883 | Rare:68 | ||||
| chr17:42329412-42329581 | Common:1; Rare:51; Clinvar (benign):3 | ||||
| chr17:42428620-42429030 | Common:1; Rare:72 |