| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83012808-83013263 | Common:2; Rare:120 | ||||
| chr4:83034789-83035227 | Common:1; Rare:106 | ||||
| chr4:83109834-83110042 | Rare:51 | ||||
| chr4:83114697-83114810 | Common:2; Rare:26 | ||||
| chr4:83284610-83284895 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr4:83334794-83334981 | Rare:44 | ||||
| chr4:83455787-83456165 | Common:2; Rare:151 | ||||
| chr4:83485031-83485287 | Common:4; Rare:117; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:83535979-83536154 | Common:1; Rare:46 | ||||
| chr4:83536159-83536541 | Rare:113 | ||||
| chr4:84966643-84966821 | Rare:44 | ||||
| chr4:86594055-86594353 | Rare:96 | ||||
| chr4:86892323-86892421 | Common:1; Rare:34 | ||||
| chr4:86934892-86935061 | Common:2; Rare:75 | ||||
| chr4:87006875-87007261 | Common:4; Rare:102 |