| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196942344-196942650 | Common:1; Rare:131 | ||||
| chr3:197736847-197737128 | Common:3; Rare:87 | ||||
| chr3:197749593-197749962 | Common:1; Rare:120 | ||||
| chr3:197791102-197791280 | Common:2; Rare:60 | ||||
| chr3:197949893-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959960-197960245 | Common:1; Rare:100 | ||||
| chr4:53022-53412 | Rare:6 | ||||
| chr4:337632-337873 | Common:1; Rare:72 | ||||
| chr4:499108-499315 | Common:3; Rare:84 | ||||
| chr4:663495-663725 | Common:1; Rare:69 | ||||
| chr4:674243-674558 | Common:1; Rare:147 | ||||
| chr4:932181-932487 | Common:2; Rare:119 | ||||
| chr4:986930-987206 | Common:3; Rare:91; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:1113554-1113582 | Rare:9 | ||||
| chr4:2041911-2042026 | Common:1; Rare:46 |