| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173530145-173530529 | Common:3; Rare:79 | ||||
| chr4:174283436-174283953 | Common:2; Rare:94 | ||||
| chr4:176319920-176320040 | Common:2; Rare:52 | ||||
| chr4:177442376-177442530 | Rare:93; Clinvar:2 | ||||
| chr4:183504529-183504792 | Common:1; Rare:88 | ||||
| chr4:183659112-183659401 | Common:1; Rare:98 | ||||
| chr4:184649434-184649773 | Common:4; Rare:110 | ||||
| chr4:184825931-184826256 | Common:7; Rare:104 | ||||
| chr4:185396563-185396850 | Rare:93 | ||||
| chr4:185425870-185426255 | Common:4; Rare:115 | ||||
| chr4:185471078-185471412 | Common:10; Rare:37 | ||||
| chr4:185535341-185535703 | Common:3; Rare:126; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185657299-185657481 | Common:2; Rare:51 | ||||
| chr4:185761561-185761854 | Common:2; Rare:46 | ||||
| chr4:185775790-185775997 | Common:1; Rare:33 |