| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:499149-499297 | Common:2; Rare:51 | ||||
| chr4:663410-663734 | Common:1; Rare:96 | ||||
| chr4:673822-673940 | Common:1; Rare:44 | ||||
| chr4:674210-674573 | Common:3; Rare:167 | ||||
| chr4:680895-681228 | Rare:117 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:1113537-1113627 | Common:1; Rare:34 | ||||
| chr4:1346941-1347210 | Common:4; Rare:74 | ||||
| chr4:1720522-1720608 | Rare:19 | ||||
| chr4:2468878-2469167 | Common:4; Rare:108 | ||||
| chr4:2843678-2844022 | Common:3; Rare:125 | ||||
| chr4:2934768-2934910 | Common:1; Rare:66 | ||||
| chr4:2963315-2963597 | Common:2; Rare:107 | ||||
| chr4:3463151-3463378 | Common:3; Rare:76; Clinvar (benign):2 | ||||
| chr4:3532208-3532336 | Rare:45; Clinvar (pathogenic):2 |