| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55395860-55395968 | Rare:28; Clinvar:2 | ||||
| chr4:55423407-55423625 | Common:6; Rare:38 | ||||
| chr4:55546801-55546862 | Rare:15 | ||||
| chr4:55546883-55547182 | Common:2; Rare:115 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435478-56435752 | Common:5; Rare:103 | ||||
| chr4:56435994-56436315 | Rare:115 | ||||
| chr4:56467542-56467735 | Common:2; Rare:77; Clinvar (benign):5 | ||||
| chr4:56977597-56977777 | Common:1; Rare:62 | ||||
| chr4:57109850-57110180 | Rare:115 | ||||
| chr4:67545377-67545721 | Common:2; Rare:79 | ||||
| chr4:67701117-67701391 | Common:4; Rare:125 | ||||
| chr4:68349952-68350209 | Common:1; Rare:95 | ||||
| chr4:70688182-70688599 | Common:2; Rare:104 | ||||
| chr4:70993482-70993649 | Common:4; Rare:49 |