| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74444940-74445144 | Common:1; Rare:38 | ||||
| chr4:75514272-75514505 | Common:1; Rare:80 | ||||
| chr4:75673088-75673222 | Rare:31 | ||||
| chr4:75673332-75673692 | Common:1; Rare:145 | ||||
| chr4:75724375-75724794 | Common:2; Rare:125 | ||||
| chr4:76147833-76147906 | Rare:19 | ||||
| chr4:76148357-76148577 | Common:3; Rare:70 | ||||
| chr4:76306367-76306756 | Common:2; Rare:94 | ||||
| chr4:76949559-76949884 | Common:2; Rare:108 | ||||
| chr4:77075965-77076107 | Common:3; Rare:73 | ||||
| chr4:77862650-77862895 | Common:3; Rare:99 | ||||
| chr4:80072674-80072849 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr4:82373915-82374309 | Common:3; Rare:119 | ||||
| chr4:82891035-82891409 | Common:2; Rare:145 | ||||
| chr4:82900474-82900792 | Rare:98 |