| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41688786-41689079 | Common:2; Rare:134 | ||||
| chr17:41689295-41689647 | Common:4; Rare:126 | ||||
| chr17:41785202-41785391 | Common:1; Rare:40 | ||||
| chr17:41812567-41813019 | Common:3; Rare:101; Clinvar:5 | ||||
| chr17:41835847-41836060 | Rare:67 | ||||
| chr17:41918882-41919047 | Rare:79; Clinvar:1 | ||||
| chr17:41930484-41930666 | Rare:54 | ||||
| chr17:41966503-41966845 | Common:3; Rare:106 | ||||
| chr17:42017372-42017580 | Common:1; Rare:79 | ||||
| chr17:42120954-42121218 | Rare:65 | ||||
| chr17:42276284-42276658 | Common:1; Rare:128 | ||||
| chr17:42388304-42388541 | Rare:70; Clinvar:4 | ||||
| chr17:42423177-42423462 | Common:1; Rare:73; Clinvar:1 | ||||
| chr17:42458697-42458941 | Common:3; Rare:90 | ||||
| chr17:42536140-42536302 | Rare:48; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 |