| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40038881-40039389 | Common:3; Rare:176 | ||||
| chr15:40106589-40106818 | Rare:39 | ||||
| chr15:40106931-40107121 | Rare:23 | ||||
| chr15:40108126-40108212 | Rare:23 | ||||
| chr15:40108829-40109182 | Common:1; Rare:93 | ||||
| chr15:40109260-40109348 | Rare:18 | ||||
| chr15:40160833-40161341 | Common:8; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:40161370-40161488 | Rare:24 | ||||
| chr15:40161494-40161656 | Rare:27 | ||||
| chr15:40239108-40239424 | Common:1; Rare:69 | ||||
| chr15:40252541-40252893 | Common:2; Rare:126 | ||||
| chr15:40252897-40253085 | Rare:46 | ||||
| chr15:40281990-40282260 | Common:1; Rare:74 | ||||
| chr15:40291321-40291484 | Common:2; Rare:54 | ||||
| chr15:40338136-40338379 | Rare:47 |