| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184825954-184826194 | Common:5; Rare:80 | ||||
| chr4:185203886-185204026 | Rare:42 | ||||
| chr4:185209422-185209659 | Common:1; Rare:82 | ||||
| chr4:185396389-185396843 | Rare:151 | ||||
| chr4:185425963-185426272 | Common:2; Rare:80 | ||||
| chr4:185471039-185471432 | Common:11; Rare:55 | ||||
| chr4:185471701-185471742 | Rare:18 | ||||
| chr4:185656695-185656780 | Rare:18 | ||||
| chr4:186104558-186104744 | Common:2; Rare:62 | ||||
| chr4:186105092-186105276 | Common:1; Rare:66 | ||||
| chr4:186191447-186191645 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:186226172-186226409 | Common:3; Rare:33 | ||||
| chr4:186250044-186250569 | Common:3; Rare:129; Clinvar (benign):1 | ||||
| chr4:186251227-186251539 | Rare:79; Clinvar (benign):1 | ||||
| chr4:186723769-186723890 | Common:4; Rare:49 |