| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40318062-40318300 | Common:1; Rare:50 | ||||
| chr17:40342014-40342403 | Common:2; Rare:170 | ||||
| chr17:40345580-40346050 | Common:3; Rare:81 | ||||
| chr17:40417844-40418188 | Rare:201 | ||||
| chr17:40443279-40443504 | Common:1; Rare:121 | ||||
| chr17:40818684-40819450 | Common:27; Rare:637; Clinvar (benign):4 | ||||
| chr17:41688590-41689027 | Common:4; Rare:321 | ||||
| chr17:41689277-41689582 | Common:6; Rare:221 | ||||
| chr17:41772660-41773120 | Common:4; Rare:112 | ||||
| chr17:41811900-41812330 | Rare:177 | ||||
| chr17:41812320-41812510 | Common:2; Rare:89 | ||||
| chr17:41812567-41813280 | Common:6; Rare:352; Clinvar:18 | ||||
| chr17:41818100-41818760 | Common:2; Rare:334; Clinvar:14; Clinvar (benign):4 | ||||
| chr17:41836095-41836324 | Rare:103 | ||||
| chr17:41865366-41865611 | Common:1; Rare:183 |