| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41214440-41214740 | Common:5; Rare:77 | ||||
| chr4:41256719-41257007 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41261711-41261922 | Rare:78; Clinvar:1 | ||||
| chr4:41359505-41359631 | Rare:21 | ||||
| chr4:41360699-41360837 | Common:1; Rare:40 | ||||
| chr4:41748032-41748308 | Rare:37 | ||||
| chr4:41748315-41748540 | Rare:54; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr4:41748547-41748577 | Rare:9; Clinvar:2 | ||||
| chr4:41748706-41749043 | Rare:53; Clinvar:1 | ||||
| chr4:41749128-41749325 | Common:3; Rare:38 | ||||
| chr4:41934986-41935381 | Common:3; Rare:108 | ||||
| chr4:41935383-41935487 | Common:1; Rare:32 | ||||
| chr4:41990379-41990602 | Common:1; Rare:80 | ||||
| chr4:42656948-42657311 | Common:7; Rare:126 | ||||
| chr4:44448918-44449122 | Common:1; Rare:66 |