| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177442376-177442530 | Rare:93; Clinvar:2 | ||||
| chr4:182917319-182917521 | Common:3; Rare:78 | ||||
| chr4:183504522-183504792 | Common:1; Rare:91 | ||||
| chr4:183659057-183659417 | Common:1; Rare:113 | ||||
| chr4:184474504-184474823 | Rare:74 | ||||
| chr4:184649412-184649794 | Common:4; Rare:124 | ||||
| chr4:184734125-184734419 | Common:6; Rare:88 | ||||
| chr4:184805525-184805853 | Common:2; Rare:59 | ||||
| chr4:185143162-185143284 | Common:1; Rare:40; Clinvar (benign):2 | ||||
| chr4:185203906-185204097 | Rare:64 | ||||
| chr4:185396563-185396843 | Rare:90 | ||||
| chr4:185425870-185426265 | Common:4; Rare:121 | ||||
| chr4:185471056-185471412 | Common:10; Rare:44 | ||||
| chr4:185535378-185535640 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):8 | ||||
| chr4:186191625-186191829 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):4 |