| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184474504-184474838 | Rare:77 | ||||
| chr4:184649399-184649796 | Common:4; Rare:130 | ||||
| chr4:184734048-184734408 | Common:5; Rare:131 | ||||
| chr4:184805465-184805828 | Common:1; Rare:68 | ||||
| chr4:184808474-184808614 | Rare:26 | ||||
| chr4:185142927-185143483 | Common:6; Rare:158; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:185395885-185396011 | Common:1; Rare:37 | ||||
| chr4:185396563-185396851 | Rare:93 | ||||
| chr4:185396993-185397237 | Rare:88 | ||||
| chr4:185425870-185426267 | Common:4; Rare:121 | ||||
| chr4:185471054-185471412 | Common:10; Rare:46 | ||||
| chr4:185535341-185535647 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185775730-185775999 | Common:1; Rare:43 | ||||
| chr4:185811645-185812271 | Common:2; Rare:116 | ||||
| chr4:185812312-185812606 | Common:1; Rare:58 |