| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:760995-761318 | Common:2; Rare:107 | ||||
| chr4:764814-764995 | Common:2; Rare:74 | ||||
| chr4:773241-773366 | Common:1; Rare:23 | ||||
| chr4:781823-782166 | Common:2; Rare:115 | ||||
| chr4:786946-787112 | Common:1; Rare:39 | ||||
| chr4:1167514-1167885 | Common:2; Rare:161 | ||||
| chr4:1243743-1244041 | Rare:72 | ||||
| chr4:1245926-1246082 | Common:1; Rare:37 | ||||
| chr4:1246315-1246539 | Common:1; Rare:54 | ||||
| chr4:1806001-1806326 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr4:2862601-2862816 | Rare:43 | ||||
| chr4:2942230-2942488 | Common:1; Rare:94 | ||||
| chr4:2951114-2951367 | Common:1; Rare:86 | ||||
| chr4:3041317-3041828 | Common:8; Rare:121 | ||||
| chr4:3503268-3503271 |