| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134648562-134648685 | Common:1; Rare:20 | ||||
| chr5:134648688-134648890 | Rare:60 | ||||
| chr5:134874261-134874423 | Common:1; Rare:82 | ||||
| chr5:134905074-134905201 | Common:1; Rare:34 | ||||
| chr5:135578920-135579174 | Common:2; Rare:72 | ||||
| chr5:137753828-137754078 | Rare:47 | ||||
| chr5:137889323-137889422 | Common:1; Rare:34 | ||||
| chr5:138033030-138033182 | Common:1; Rare:54 | ||||
| chr5:138337978-138338289 | Common:1; Rare:119 | ||||
| chr5:138465843-138465856 | Rare:5 | ||||
| chr5:138543060-138543544 | Common:3; Rare:146 | ||||
| chr5:138558594-138558768 | Common:1; Rare:46; Clinvar:1 | ||||
| chr5:138753277-138753503 | Common:2; Rare:77 | ||||
| chr5:138886159-138886285 | Rare:26 | ||||
| chr5:138930343-138930654 | Common:1; Rare:61; Clinvar (benign):1 |