| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197749682-197749962 | Common:1; Rare:94 | ||||
| chr3:197791142-197791274 | Common:1; Rare:46 | ||||
| chr3:197949885-197950252 | Common:4; Rare:112; Clinvar (benign):2 | ||||
| chr3:197959979-197960248 | Common:1; Rare:93 | ||||
| chr4:337482-337826 | Common:1; Rare:87 | ||||
| chr4:499136-499319 | Common:3; Rare:68 | ||||
| chr4:673871-673958 | Rare:40 | ||||
| chr4:674243-674614 | Common:3; Rare:173 | ||||
| chr4:681104-681227 | Rare:48 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:1113544-1113632 | Common:1; Rare:32 | ||||
| chr4:1201537-1201790 | Rare:70 | ||||
| chr4:1289693-1289922 | Common:1; Rare:76 | ||||
| chr4:1309376-1309641 | Common:3; Rare:72 | ||||
| chr4:1721325-1721549 | Common:4; Rare:65 |