| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83012392-83012515 | Rare:25 | ||||
| chr4:83012799-83013318 | Common:2; Rare:133 | ||||
| chr4:83034333-83034447 | Rare:22 | ||||
| chr4:83034586-83034665 | Common:5; Rare:16 | ||||
| chr4:83034732-83035269 | Common:3; Rare:132 | ||||
| chr4:83035805-83035894 | Rare:11 | ||||
| chr4:83109647-83109750 | Common:1; Rare:22 | ||||
| chr4:83109774-83110182 | Common:3; Rare:91 | ||||
| chr4:83114700-83114758 | Rare:14 | ||||
| chr4:83284400-83284602 | Common:2; Rare:74; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:83284694-83284895 | Common:3; Rare:84; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr4:83334823-83335042 | Rare:43 | ||||
| chr4:83455466-83455600 | Rare:59 | ||||
| chr4:83455739-83456172 | Common:3; Rare:173 | ||||
| chr4:83485044-83485355 | Common:4; Rare:134; Clinvar:1; Clinvar (benign):3 |