| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39638815-39639154 | Common:1; Rare:120 | ||||
| chr4:39697981-39698192 | Common:1; Rare:83 | ||||
| chr4:39977310-39977640 | Common:2; Rare:96 | ||||
| chr4:40056603-40056957 | Common:4; Rare:105 | ||||
| chr4:40057219-40057508 | Common:1; Rare:71 | ||||
| chr4:40193320-40193564 | Common:1; Rare:39 | ||||
| chr4:40200032-40200389 | Common:1; Rare:67 | ||||
| chr4:40629467-40629946 | Common:1; Rare:105 | ||||
| chr4:40630130-40630199 | Common:1; Rare:7 | ||||
| chr4:40630544-40630811 | Common:2; Rare:59 | ||||
| chr4:40630829-40630929 | Rare:25 | ||||
| chr4:41214433-41214764 | Common:5; Rare:82 | ||||
| chr4:41256703-41257125 | Common:4; Rare:136; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261711-41261923 | Rare:79; Clinvar:1 | ||||
| chr4:41359488-41359776 | Rare:45 |