| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56387423-56387547 | Rare:44 | ||||
| chr4:56435541-56435770 | Common:3; Rare:77 | ||||
| chr4:56467521-56467668 | Common:2; Rare:61; Clinvar (benign):4 | ||||
| chr4:56977138-56977318 | Rare:77 | ||||
| chr4:56977574-56977747 | Common:1; Rare:67 | ||||
| chr4:67701111-67701423 | Common:4; Rare:142 | ||||
| chr4:70688182-70688592 | Common:2; Rare:103 | ||||
| chr4:70688644-70689061 | Common:2; Rare:123 | ||||
| chr4:70704652-70704816 | Common:1; Rare:49 | ||||
| chr4:70839232-70839368 | Common:2; Rare:51 | ||||
| chr4:70902221-70902382 | Common:4; Rare:55 | ||||
| chr4:70993470-70993662 | Common:5; Rare:61 | ||||
| chr4:71187069-71187363 | Common:2; Rare:92 | ||||
| chr4:73104190-73104325 | Common:1; Rare:20 | ||||
| chr4:73258434-73258919 | Common:1; Rare:148 |