| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197949890-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959989-197960245 | Common:1; Rare:90 | ||||
| chr4:337470-337873 | Common:2; Rare:118 | ||||
| chr4:499132-499329 | Common:3; Rare:75 | ||||
| chr4:663611-663725 | Rare:36 | ||||
| chr4:674213-674560 | Common:2; Rare:161 | ||||
| chr4:705589-705838 | Rare:83 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:986920-987029 | Common:1; Rare:29; Clinvar:1 | ||||
| chr4:1113524-1113632 | Common:2; Rare:39 | ||||
| chr4:1172791-1172917 | Common:3; Rare:19 | ||||
| chr4:1289659-1289916 | Common:1; Rare:84 | ||||
| chr4:1347038-1347210 | Common:2; Rare:52 | ||||
| chr4:1720332-1720597 | Common:2; Rare:71 | ||||
| chr4:2468880-2469167 | Common:4; Rare:108 |