| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83455752-83456078 | Common:3; Rare:122 | ||||
| chr4:83485050-83485348 | Common:4; Rare:132; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:84496305-84496500 | Common:2; Rare:41 | ||||
| chr4:84496879-84497279 | Common:3; Rare:109 | ||||
| chr4:84498478-84499183 | Common:9; Rare:204 | ||||
| chr4:84582658-84582902 | Common:1; Rare:62 | ||||
| chr4:84966722-84967064 | Rare:86 | ||||
| chr4:85474987-85475178 | Common:1; Rare:32 | ||||
| chr4:85475529-85475758 | Rare:25 | ||||
| chr4:85929970-85930433 | Common:6; Rare:147 | ||||
| chr4:86357220-86357905 | Common:5; Rare:158 | ||||
| chr4:86358029-86358474 | Common:2; Rare:149 | ||||
| chr4:86359229-86359483 | Common:8; Rare:64 | ||||
| chr4:86360012-86360491 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:86594017-86594375 | Rare:110 |