| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177442287-177442530 | Common:1; Rare:136; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr4:182917325-182917619 | Common:4; Rare:93 | ||||
| chr4:183444342-183444818 | Common:2; Rare:198 | ||||
| chr4:183504501-183504817 | Common:3; Rare:101 | ||||
| chr4:183505980-183506116 | Rare:53 | ||||
| chr4:183659122-183659411 | Common:1; Rare:95 | ||||
| chr4:184474504-184474816 | Rare:69 | ||||
| chr4:184649406-184649805 | Common:4; Rare:129 | ||||
| chr4:184805461-184805832 | Common:1; Rare:69 | ||||
| chr4:185142982-185143285 | Common:3; Rare:82; Clinvar (benign):2 | ||||
| chr4:185203857-185204136 | Common:5; Rare:88 | ||||
| chr4:185395729-185396005 | Common:2; Rare:65 | ||||
| chr4:185396581-185396843 | Rare:83 | ||||
| chr4:185425872-185426278 | Common:4; Rare:122 | ||||
| chr4:185535438-185535655 | Common:1; Rare:74; Clinvar (benign):3 |