| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:182917287-182917616 | Common:4; Rare:100 | ||||
| chr4:183444407-183444776 | Common:2; Rare:172 | ||||
| chr4:183504390-183504771 | Common:1; Rare:126 | ||||
| chr4:183504990-183505364 | Common:5; Rare:111 | ||||
| chr4:183659156-183659382 | Common:1; Rare:74 | ||||
| chr4:183684201-183684322 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:184474461-184474693 | Rare:50 | ||||
| chr4:184649399-184649789 | Common:4; Rare:130 | ||||
| chr4:185203915-185204263 | Common:4; Rare:114 | ||||
| chr4:185395910-185396099 | Rare:58 | ||||
| chr4:185396431-185396885 | Rare:157 | ||||
| chr4:185397010-185397285 | Rare:100 | ||||
| chr4:185425875-185426265 | Common:4; Rare:118 | ||||
| chr4:185535363-185535609 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:186726442-186726818 | Common:6; Rare:103 |