| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77862650-77862877 | Common:3; Rare:86 | ||||
| chr4:78057601-78057604 | |||||
| chr4:78551495-78551647 | Rare:27 | ||||
| chr4:78551651-78551847 | Rare:50 | ||||
| chr4:80072682-80072845 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr4:80073063-80073174 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:82373887-82374343 | Common:3; Rare:145 | ||||
| chr4:82429320-82429572 | Common:1; Rare:156; Clinvar:7; Clinvar (benign):5 | ||||
| chr4:82430452-82430634 | Rare:66 | ||||
| chr4:82430757-82430832 | Rare:34 | ||||
| chr4:82891035-82891409 | Common:2; Rare:145 | ||||
| chr4:82900479-82900741 | Rare:74 | ||||
| chr4:83010747-83010914 | Rare:27 | ||||
| chr4:83455800-83456089 | Common:2; Rare:114 | ||||
| chr4:83485093-83485310 | Common:3; Rare:92 |