| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:76148363-76148577 | Common:3; Rare:67 | ||||
| chr4:76251562-76251739 | Rare:43 | ||||
| chr4:76897970-76898287 | Common:1; Rare:73 | ||||
| chr4:76949569-76949883 | Common:2; Rare:103 | ||||
| chr4:76987694-76987756 | Rare:13 | ||||
| chr4:77028366-77028759 | Common:3; Rare:74 | ||||
| chr4:77055316-77055556 | Rare:66 | ||||
| chr4:77075557-77075822 | Common:2; Rare:101 | ||||
| chr4:77075965-77076122 | Common:3; Rare:80 | ||||
| chr4:77862643-77862851 | Common:2; Rare:70 | ||||
| chr4:78057487-78057604 | Common:2; Rare:26 | ||||
| chr4:78939246-78939541 | Common:2; Rare:133 | ||||
| chr4:80073026-80073252 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:81471798-81472060 | Common:1; Rare:82 | ||||
| chr4:82373891-82374317 | Common:3; Rare:127 |