| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52659204-52659416 | Common:1; Rare:74 | ||||
| chr4:54064427-54064463 | Rare:11 | ||||
| chr4:55125583-55125694 | Common:2; Rare:25 | ||||
| chr4:55346179-55346339 | Common:3; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55546813-55546977 | Common:1; Rare:57 | ||||
| chr4:55948720-55948875 | Rare:33 | ||||
| chr4:56387394-56387528 | Rare:47 | ||||
| chr4:56435473-56435752 | Common:5; Rare:104 | ||||
| chr4:56435967-56436307 | Rare:123 | ||||
| chr4:56467527-56467699 | Common:2; Rare:72; Clinvar (benign):5 | ||||
| chr4:56977570-56977771 | Common:1; Rare:77 | ||||
| chr4:65670482-65670550 | Rare:18 | ||||
| chr4:67545400-67545723 | Common:2; Rare:75 | ||||
| chr4:67701089-67701377 | Common:4; Rare:136 | ||||
| chr4:68349952-68350228 | Common:2; Rare:100 |