| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47485166-47485408 | Common:2; Rare:76 | ||||
| chr4:48269807-48269989 | Common:1; Rare:37 | ||||
| chr4:48341114-48341629 | Common:2; Rare:200 | ||||
| chr4:48341777-48341968 | Rare:55 | ||||
| chr4:51843345-51843564 | Rare:73 | ||||
| chr4:52659204-52659420 | Common:1; Rare:75 | ||||
| chr4:53377434-53377766 | Common:4; Rare:106 | ||||
| chr4:54064410-54064463 | Rare:13 | ||||
| chr4:55395816-55395968 | Common:2; Rare:38; Clinvar:2 | ||||
| chr4:55546805-55546998 | Common:2; Rare:66 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435484-56435736 | Common:5; Rare:93 | ||||
| chr4:56467527-56467689 | Common:2; Rare:69; Clinvar (benign):4 | ||||
| chr4:56655994-56656126 | Common:3; Rare:50 | ||||
| chr4:56656301-56656533 | Common:3; Rare:41 |