| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:337342-337877 | Common:4; Rare:151 | ||||
| chr4:499123-499319 | Common:3; Rare:77 | ||||
| chr4:663585-663725 | Rare:45 | ||||
| chr4:674243-674558 | Common:1; Rare:147 | ||||
| chr4:681131-681232 | Rare:41 | ||||
| chr4:705860-705958 | Rare:37 | ||||
| chr4:932212-932487 | Common:2; Rare:107 | ||||
| chr4:986904-987165 | Common:3; Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113524-1113644 | Common:2; Rare:46 | ||||
| chr4:1346817-1347083 | Common:4; Rare:78 | ||||
| chr4:2041909-2042017 | Common:1; Rare:41 | ||||
| chr4:2468888-2469163 | Common:2; Rare:103 | ||||
| chr4:2843687-2844022 | Common:3; Rare:121 | ||||
| chr4:2934767-2934910 | Common:1; Rare:66 | ||||
| chr4:3074536-3074692 | Common:3; Rare:46 |