| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43330525-43330742 | Common:1; Rare:76 | ||||
| chr15:43371030-43371113 | Rare:18 | ||||
| chr15:43493065-43493364 | Common:1; Rare:95 | ||||
| chr15:43510688-43510964 | Rare:88 | ||||
| chr15:43746257-43746702 | Common:3; Rare:174 | ||||
| chr15:43776963-43777409 | Rare:110 | ||||
| chr15:43792724-43793083 | Rare:105 | ||||
| chr15:43824603-43824791 | Common:2; Rare:52 | ||||
| chr15:44427381-44427660 | Common:1; Rare:61 | ||||
| chr15:44536663-44536727 | Rare:11 | ||||
| chr15:44536855-44537227 | Common:3; Rare:138 | ||||
| chr15:44711314-44711611 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44712007 | Rare:29 | ||||
| chr15:44712617-44712865 | Rare:64 | ||||
| chr15:44728716-44729232 | Common:1; Rare:102 |