| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736891-197737149 | Common:2; Rare:82 | ||||
| chr3:197749695-197750007 | Common:1; Rare:106 | ||||
| chr3:197791134-197791275 | Common:1; Rare:48 | ||||
| chr3:197949873-197950266 | Common:4; Rare:116; Clinvar (benign):2 | ||||
| chr3:197959971-197960255 | Common:1; Rare:100 | ||||
| chr4:499141-499307 | Common:2; Rare:61 | ||||
| chr4:674211-674558 | Common:2; Rare:159 | ||||
| chr4:932259-932492 | Common:2; Rare:90 | ||||
| chr4:986928-987088 | Rare:45; Clinvar:1 | ||||
| chr4:1248681-1248957 | Common:4; Rare:104 | ||||
| chr4:1249090-1249263 | Common:1; Rare:44 | ||||
| chr4:1289663-1289912 | Common:1; Rare:80 | ||||
| chr4:1309403-1309649 | Common:3; Rare:66 | ||||
| chr4:1346763-1347242 | Common:6; Rare:144 | ||||
| chr4:1712310-1712486 | Common:2; Rare:54 |