| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435475-56435758 | Common:5; Rare:103 | ||||
| chr4:56435966-56436307 | Rare:124 | ||||
| chr4:56467507-56467699 | Common:2; Rare:80; Clinvar (benign):5 | ||||
| chr4:56681585-56681847 | Common:1; Rare:39 | ||||
| chr4:56907791-56907992 | Common:3; Rare:78 | ||||
| chr4:56908130-56908180 | Rare:7 | ||||
| chr4:56977352-56977771 | Common:3; Rare:153 | ||||
| chr4:57023186-57023353 | Common:1; Rare:32 | ||||
| chr4:57023486-57023751 | Common:1; Rare:42 | ||||
| chr4:57110332-57110536 | Common:1; Rare:64 | ||||
| chr4:65670487-65670606 | Rare:31 | ||||
| chr4:67545358-67545748 | Common:2; Rare:95 | ||||
| chr4:67701115-67701398 | Common:4; Rare:132 | ||||
| chr4:68349878-68350200 | Rare:103 |