| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43493035-43493350 | Common:2; Rare:105 | ||||
| chr15:43510587-43511104 | Rare:189 | ||||
| chr15:43517462-43517653 | Common:2; Rare:43 | ||||
| chr15:43746261-43746704 | Common:3; Rare:174 | ||||
| chr15:43824554-43824818 | Common:2; Rare:78 | ||||
| chr15:43826905-43827092 | Rare:79 | ||||
| chr15:44288409-44289048 | Common:39; Rare:303 | ||||
| chr15:44427007-44427409 | Common:1; Rare:114 | ||||
| chr15:44427552-44427720 | Common:1; Rare:47 | ||||
| chr15:44536533-44536653 | Rare:24 | ||||
| chr15:44536855-44537425 | Common:3; Rare:204 | ||||
| chr15:44663543-44663845 | Rare:146; Clinvar:12; Clinvar (benign):6 | ||||
| chr15:44711354-44711595 | Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728845-44729198 | Common:1; Rare:73 | ||||
| chr15:45023051-45023248 | Common:3; Rare:53 |