| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:51842762-51843224 | Common:1; Rare:134 | ||||
| chr4:52659188-52659554 | Common:1; Rare:116 | ||||
| chr4:53365959-53366136 | Rare:34 | ||||
| chr4:55125471-55125713 | Common:3; Rare:57 | ||||
| chr4:55546865-55547204 | Common:3; Rare:134 | ||||
| chr4:56387170-56387230 | Rare:14 | ||||
| chr4:56387414-56387582 | Rare:61 | ||||
| chr4:56435473-56435770 | Common:5; Rare:107 | ||||
| chr4:56435994-56436315 | Rare:115 | ||||
| chr4:56467521-56467578 | Rare:18 | ||||
| chr4:56467579-56467684 | Common:2; Rare:49; Clinvar (benign):4 | ||||
| chr4:56530426-56530670 | Common:4; Rare:68 | ||||
| chr4:56977547-56977785 | Common:2; Rare:90 | ||||
| chr4:67545402-67545742 | Common:2; Rare:83 | ||||
| chr4:67701111-67701419 | Common:4; Rare:142 |