| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42404536-42404879 | Rare:55 | ||||
| chr15:42490997-42491196 | Common:1; Rare:64 | ||||
| chr15:42495478-42495694 | Common:2; Rare:62 | ||||
| chr15:42511664-42511901 | Common:1; Rare:43 | ||||
| chr15:42548711-42548890 | Common:2; Rare:98 | ||||
| chr15:43106011-43106174 | Rare:48 | ||||
| chr15:43185179-43185501 | Common:1; Rare:99 | ||||
| chr15:43330537-43330726 | Common:1; Rare:68 | ||||
| chr15:43371021-43371231 | Common:1; Rare:43 | ||||
| chr15:43493061-43493322 | Common:1; Rare:82 | ||||
| chr15:43510581-43511112 | Rare:194 | ||||
| chr15:43517456-43517659 | Common:2; Rare:48 | ||||
| chr15:44427559-44427653 | Rare:28 | ||||
| chr15:44536855-44537200 | Common:1; Rare:120 | ||||
| chr15:44663532-44663861 | Rare:156; Clinvar:13; Clinvar (benign):6 |