| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:674229-674585 | Common:5; Rare:331 | ||||
| chr4:687252-687488 | Rare:101 | ||||
| chr4:705533-705887 | Common:2; Rare:208 | ||||
| chr4:932077-932527 | Common:4; Rare:285 | ||||
| chr4:986810-987190 | Common:6; Rare:192; Clinvar:5; Clinvar (benign):4 | ||||
| chr4:992550-993101 | Common:5; Rare:274 | ||||
| chr4:1011298-1011681 | Common:8; Rare:180 | ||||
| chr4:1113473-1113692 | Common:7; Rare:136 | ||||
| chr4:1248324-1248454 | Common:1; Rare:47 | ||||
| chr4:1248610-1248990 | Common:7; Rare:244 | ||||
| chr4:1249057-1249507 | Common:8; Rare:253 | ||||
| chr4:1289641-1289915 | Common:2; Rare:180 | ||||
| chr4:1346893-1347348 | Common:10; Rare:262 | ||||
| chr4:1684240-1684650 | Common:6; Rare:282 | ||||
| chr4:1712224-1712559 | Common:5; Rare:204 |