| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196318184-196318340 | Common:1; Rare:65 | ||||
| chr3:196712228-196712320 | Common:2; Rare:29 | ||||
| chr3:196942375-196942702 | Common:1; Rare:141 | ||||
| chr3:197949896-197950250 | Common:4; Rare:108; Clinvar (benign):2 | ||||
| chr4:674238-674558 | Common:1; Rare:149 | ||||
| chr4:932290-932434 | Common:2; Rare:57 | ||||
| chr4:2041912-2042011 | Common:1; Rare:38 | ||||
| chr4:2468929-2469167 | Common:2; Rare:80 | ||||
| chr4:2934777-2934886 | Common:1; Rare:50 | ||||
| chr4:4248201-4248260 | Common:1; Rare:24 | ||||
| chr4:4290117-4290226 | Common:1; Rare:42 | ||||
| chr4:4541970-4542137 | Common:1; Rare:71 | ||||
| chr4:15681564-15681863 | Common:3; Rare:106 | ||||
| chr4:17614553-17614647 | Common:2; Rare:40 | ||||
| chr4:17810701-17811024 | Common:3; Rare:97 |