| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600359-42600757 | Common:2; Rare:155 | ||||
| chr3:42804422-42804657 | Common:2; Rare:68 | ||||
| chr3:43286470-43286661 | Common:2; Rare:82 | ||||
| chr3:43621914-43622178 | Common:2; Rare:93; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43690993 | Common:3; Rare:95; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338086-44338187 | Common:2; Rare:37 | ||||
| chr3:44338319-44338463 | Common:2; Rare:48 | ||||
| chr3:44338694-44338797 | Common:3; Rare:38 | ||||
| chr3:44477655-44477707 | Common:1; Rare:10 | ||||
| chr3:44624845-44625086 | Common:2; Rare:69 | ||||
| chr3:44761571-44761817 | Common:3; Rare:96 | ||||
| chr3:44861796-44861931 | Common:2; Rare:63 | ||||
| chr3:44976107-44976278 | Common:2; Rare:69 | ||||
| chr3:45388436-45388636 | Common:1; Rare:54 | ||||
| chr3:45689180-45689459 | Common:1; Rare:93 |