| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56387397-56387556 | Rare:55 | ||||
| chr4:56435353-56435383 | Rare:5 | ||||
| chr4:56435456-56436326 | Common:6; Rare:295 | ||||
| chr4:56467475-56467740 | Common:2; Rare:105; Clinvar (benign):5 | ||||
| chr4:56977366-56977788 | Common:3; Rare:152 | ||||
| chr4:57009121-57009408 | Common:3; Rare:52 | ||||
| chr4:57009509-57009601 | Common:1; Rare:14 | ||||
| chr4:57110055-57110192 | Rare:48 | ||||
| chr4:57110350-57110716 | Common:2; Rare:104 | ||||
| chr4:67701051-67701419 | Common:4; Rare:168 | ||||
| chr4:68349730-68349886 | Common:1; Rare:64 | ||||
| chr4:68349952-68350174 | Rare:82 | ||||
| chr4:70688808-70688960 | Rare:44 | ||||
| chr4:70688961-70689238 | Common:1; Rare:95 | ||||
| chr4:70838967-70839014 | Rare:12 |