| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:47150471-47150546 | Common:1; Rare:27 | ||||
| chr18:49460636-49460819 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49561890-49562093 | Rare:49 | ||||
| chr18:49813816-49814044 | Common:1; Rare:91 | ||||
| chr18:50878963-50879177 | Common:4; Rare:71 | ||||
| chr18:54269443-54269610 | Common:2; Rare:81 | ||||
| chr18:54357856-54357903 | Common:1; Rare:16 | ||||
| chr18:55589776-55589996 | Common:2; Rare:79 | ||||
| chr18:56651133-56651379 | Common:3; Rare:62 | ||||
| chr18:59697620-59697819 | Common:1; Rare:55 | ||||
| chr18:62186985-62187320 | Common:5; Rare:95 | ||||
| chr18:62526759-62526898 | Common:2; Rare:68 | ||||
| chr18:63367138-63367328 | Common:1; Rare:68 | ||||
| chr18:63422384-63422677 | Common:2; Rare:79 | ||||
| chr18:68715011-68715260 | Common:4; Rare:113 |