| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47914505-47914802 | Common:1; Rare:90 | ||||
| chr4:48269790-48269967 | Common:2; Rare:41 | ||||
| chr4:48341270-48341588 | Common:1; Rare:127 | ||||
| chr4:48780189-48780572 | Common:3; Rare:117 | ||||
| chr4:48830925-48831223 | Common:1; Rare:86 | ||||
| chr4:48906698-48906832 | Rare:38 | ||||
| chr4:52038228-52038402 | Rare:67; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr4:52862119-52862322 | Common:7; Rare:95 | ||||
| chr4:53377434-53377714 | Common:3; Rare:85 | ||||
| chr4:54228937-54229395 | Common:1; Rare:92; Clinvar (benign):4 | ||||
| chr4:55546816-55547038 | Common:2; Rare:80 | ||||
| chr4:56387423-56387524 | Rare:35 | ||||
| chr4:56435541-56435791 | Common:3; Rare:79 | ||||
| chr4:56467521-56467654 | Rare:51 | ||||
| chr4:56977597-56977777 | Common:1; Rare:62 |