| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52659261-52659444 | Common:2; Rare:113 | ||||
| chr4:53365912-53366202 | Common:1; Rare:99 | ||||
| chr4:54064482-54064771 | Common:4; Rare:160 | ||||
| chr4:55346179-55346409 | Common:3; Rare:80; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr4:55395400-55395659 | Rare:95 | ||||
| chr4:55395783-55396151 | Common:7; Rare:211; Clinvar:4 | ||||
| chr4:55545640-55546130 | Common:6; Rare:201 | ||||
| chr4:55546812-55547011 | Common:4; Rare:133 | ||||
| chr4:55853483-55853804 | Rare:92 | ||||
| chr4:55948729-55948951 | Common:1; Rare:45 | ||||
| chr4:56048893-56049206 | Common:4; Rare:131 | ||||
| chr4:56386970-56387340 | Rare:122 | ||||
| chr4:56387417-56387556 | Rare:80 | ||||
| chr4:56434932-56435332 | Rare:137 | ||||
| chr4:56435427-56435810 | Common:10; Rare:244 |