| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183505867-183506116 | Common:1; Rare:145 | ||||
| chr4:183659156-183659404 | Common:2; Rare:156 | ||||
| chr4:184474489-184474860 | Rare:159 | ||||
| chr4:184649399-184649806 | Common:8; Rare:265 | ||||
| chr4:184733250-184733540 | Common:6; Rare:136 | ||||
| chr4:184734032-184734446 | Common:10; Rare:214 | ||||
| chr4:184805668-184805794 | Common:1; Rare:20 | ||||
| chr4:184825965-184826175 | Common:9; Rare:122 | ||||
| chr4:185143132-185143274 | Common:2; Rare:81; Clinvar (benign):4 | ||||
| chr4:185203906-185204061 | Rare:49 | ||||
| chr4:185209312-185209712 | Common:4; Rare:321 | ||||
| chr4:185395780-185396090 | Common:2; Rare:139 | ||||
| chr4:185396563-185396845 | Rare:126 | ||||
| chr4:185425880-185426272 | Common:8; Rare:227 | ||||
| chr4:185470922-185471586 | Common:43; Rare:337 |