| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139389552-139389887 | Common:2; Rare:108 | ||||
| chr3:139480758-139481015 | Common:1; Rare:38 | ||||
| chr3:139539458-139539761 | Common:3; Rare:105 | ||||
| chr3:140941609-140941962 | Common:2; Rare:124 | ||||
| chr3:141231623-141231894 | Common:2; Rare:94 | ||||
| chr3:141368214-141368572 | Rare:77 | ||||
| chr3:141402148-141402437 | Common:2; Rare:75 | ||||
| chr3:141402703-141403035 | Common:3; Rare:89 | ||||
| chr3:141403049-141403126 | Rare:18 | ||||
| chr3:141875980-141876246 | Rare:73 | ||||
| chr3:141876452-141876729 | Common:2; Rare:101 | ||||
| chr3:142225456-142225644 | Common:3; Rare:66 | ||||
| chr3:142447913-142448195 | Common:1; Rare:95 | ||||
| chr3:142578045-142578243 | Rare:31 | ||||
| chr3:142578699-142578950 | Rare:94; Clinvar:1; Clinvar (benign):1 |