| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183504529-183504829 | Common:3; Rare:98 | ||||
| chr4:183506027-183506111 | Rare:31 | ||||
| chr4:183659040-183659404 | Common:1; Rare:111 | ||||
| chr4:184474504-184474816 | Rare:69 | ||||
| chr4:184649427-184649796 | Common:4; Rare:117 | ||||
| chr4:184734073-184734383 | Common:5; Rare:106 | ||||
| chr4:185203896-185204097 | Rare:66 | ||||
| chr4:185395840-185396080 | Common:2; Rare:70 | ||||
| chr4:185396563-185396851 | Rare:93 | ||||
| chr4:185425864-185426278 | Common:4; Rare:128 | ||||
| chr4:185471090-185471412 | Common:10; Rare:31 | ||||
| chr4:185535342-185535632 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185811909-185812274 | Common:1; Rare:65 | ||||
| chr4:186191528-186191871 | Common:5; Rare:110; Clinvar:2; Clinvar (benign):4 | ||||
| chr4:186723765-186723900 | Common:4; Rare:58 |