| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959969-197960272 | Common:1; Rare:111 | ||||
| chr4:337423-337880 | Common:3; Rare:132 | ||||
| chr4:499121-499333 | Common:3; Rare:87 | ||||
| chr4:663616-663753 | Rare:47 | ||||
| chr4:674238-674573 | Common:2; Rare:156 | ||||
| chr4:678399-678570 | Common:3; Rare:44 | ||||
| chr4:681120-681227 | Rare:43 | ||||
| chr4:705602-705949 | Common:1; Rare:118 | ||||
| chr4:932118-932492 | Common:2; Rare:144 | ||||
| chr4:986929-987153 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113524-1113637 | Common:2; Rare:40 | ||||
| chr4:1309419-1309645 | Common:3; Rare:60 | ||||
| chr4:2468768-2469183 | Common:4; Rare:156 | ||||
| chr4:2934767-2934894 | Common:1; Rare:58 |