| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44427879-44427981 | Rare:20 | ||||
| chr15:44427994-44428042 | Rare:7 | ||||
| chr15:44536522-44537266 | Common:4; Rare:219 | ||||
| chr15:44663069-44663340 | Common:1; Rare:62 | ||||
| chr15:44663490-44663949 | Rare:193; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:44676826-44676853 | Rare:6 | ||||
| chr15:44710721-44710922 | Common:3; Rare:37 | ||||
| chr15:44710994-44711132 | Rare:16 | ||||
| chr15:44711196-44711669 | Rare:129; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711807-44712216 | Common:1; Rare:74 | ||||
| chr15:44712599-44712842 | Rare:63 | ||||
| chr15:44728631-44729267 | Common:1; Rare:124 | ||||
| chr15:44729385-44729645 | Common:2; Rare:59 | ||||
| chr15:44736004-44736034 | Rare:6 | ||||
| chr15:44736209-44736345 | Common:1; Rare:25 |