| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600328-42600709 | Common:3; Rare:152 | ||||
| chr3:42773220-42773345 | Common:1; Rare:34 | ||||
| chr3:42804416-42804673 | Common:2; Rare:79 | ||||
| chr3:43286459-43286630 | Common:2; Rare:77 | ||||
| chr3:43621872-43622322 | Common:2; Rare:130; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690616-43690995 | Common:6; Rare:158; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338675-44338809 | Common:3; Rare:49 | ||||
| chr3:44477641-44477707 | Common:1; Rare:17 | ||||
| chr3:44584546-44584938 | Rare:81 | ||||
| chr3:44624850-44625095 | Common:2; Rare:70 | ||||
| chr3:44761583-44761813 | Common:3; Rare:84 | ||||
| chr3:44861757-44861925 | Common:2; Rare:76 | ||||
| chr3:44976120-44976279 | Common:2; Rare:66 | ||||
| chr3:45842046-45842276 | Common:1; Rare:59 | ||||
| chr3:45995802-45995926 | Common:1; Rare:31; Clinvar:1 |