| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47914512-47914909 | Common:2; Rare:118 | ||||
| chr4:48016598-48016828 | Common:1; Rare:73 | ||||
| chr4:48269773-48270030 | Common:2; Rare:64 | ||||
| chr4:48483250-48483343 | Common:1; Rare:32 | ||||
| chr4:48906674-48906836 | Rare:43 | ||||
| chr4:48986187-48986284 | Rare:31 | ||||
| chr4:51842819-51843235 | Common:1; Rare:130 | ||||
| chr4:52659171-52659426 | Common:1; Rare:86 | ||||
| chr4:52751411-52751765 | Common:3; Rare:84 | ||||
| chr4:52862147-52862455 | Common:12; Rare:137 | ||||
| chr4:53365951-53366222 | Rare:60 | ||||
| chr4:53377539-53377857 | Common:2; Rare:110 | ||||
| chr4:54064536-54064938 | Common:5; Rare:123 | ||||
| chr4:55125489-55125736 | Common:3; Rare:61 | ||||
| chr4:55346166-55346395 | Common:3; Rare:78; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |