| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1492619-1492715 | Rare:16 | ||||
| chr17:1516582-1516971 | Common:2; Rare:138 | ||||
| chr17:1628802-1629021 | Rare:75 | ||||
| chr17:1645698-1645882 | Common:2; Rare:49 | ||||
| chr17:1684135-1684440 | Common:3; Rare:109 | ||||
| chr17:1684802-1685036 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:1762663-1762805 | Common:3; Rare:30 | ||||
| chr17:1783891-1784096 | Common:1; Rare:46 | ||||
| chr17:1829786-1830039 | Common:7; Rare:108 | ||||
| chr17:2303461-2303605 | Rare:53 | ||||
| chr17:2303728-2303987 | Common:2; Rare:97 | ||||
| chr17:2336423-2336518 | Rare:35 | ||||
| chr17:2337418-2337609 | Common:1; Rare:53 | ||||
| chr17:2511796-2511994 | Common:2; Rare:58 | ||||
| chr17:2593489-2593664 | Common:2; Rare:65 |