| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40177349-40177626 | Common:1; Rare:95 | ||||
| chr17:40318079-40318288 | Common:1; Rare:44 | ||||
| chr17:40342014-40342415 | Common:1; Rare:87 | ||||
| chr17:40884795-40884886 | Common:1; Rare:32 | ||||
| chr17:41524582-41525009 | Common:1; Rare:108; Clinvar:1 | ||||
| chr17:41525060-41525317 | Common:2; Rare:81; Clinvar:1 | ||||
| chr17:41528365-41528532 | Rare:33 | ||||
| chr17:41583320-41583570 | Rare:76; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr17:41688613-41689091 | Common:3; Rare:192 | ||||
| chr17:41930532-41930629 | Rare:26 | ||||
| chr17:42017361-42017500 | Rare:62 | ||||
| chr17:42017577-42017636 | Rare:23 | ||||
| chr17:42017640-42017711 | Rare:15 | ||||
| chr17:42121317-42121423 | Common:1; Rare:30 | ||||
| chr17:42577682-42577864 | Common:1; Rare:88 |