| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48016598-48016782 | Common:1; Rare:54 | ||||
| chr4:48269795-48269973 | Common:2; Rare:37 | ||||
| chr4:48341173-48341483 | Common:1; Rare:129 | ||||
| chr4:51842822-51843212 | Common:1; Rare:116 | ||||
| chr4:52659142-52659420 | Common:1; Rare:90 | ||||
| chr4:54064505-54064771 | Common:2; Rare:87 | ||||
| chr4:55395852-55395968 | Common:1; Rare:29; Clinvar:2 | ||||
| chr4:55546796-55547012 | Common:2; Rare:74 | ||||
| chr4:56387414-56387545 | Rare:44 | ||||
| chr4:56435551-56435973 | Common:4; Rare:130 | ||||
| chr4:56467521-56467659 | Common:2; Rare:54; Clinvar (benign):4 | ||||
| chr4:56977576-56977747 | Common:1; Rare:65 | ||||
| chr4:57109877-57110202 | Rare:109 | ||||
| chr4:57110338-57110536 | Common:1; Rare:63 | ||||
| chr4:67545351-67545742 | Common:2; Rare:95 |