| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44291247-44291298 | Rare:5 | ||||
| chr15:44536058-44536167 | Common:1; Rare:18 | ||||
| chr15:44537839-44537902 | Rare:15 | ||||
| chr15:44662590-44662827 | Common:1; Rare:52 | ||||
| chr15:44672246-44672451 | Rare:40; Clinvar (pathogenic):1 | ||||
| chr15:44683332-44683556 | Rare:37 | ||||
| chr15:44710269-44710486 | Rare:32 | ||||
| chr15:44719658-44719987 | Rare:62 | ||||
| chr15:44724425-44724527 | Common:2; Rare:17 | ||||
| chr15:44726256-44726413 | Common:1; Rare:22 | ||||
| chr15:44726545-44727184 | Common:9; Rare:85 | ||||
| chr15:44727635-44727845 | Common:3; Rare:38 | ||||
| chr15:44729649-44729821 | Rare:25 | ||||
| chr15:44737983-44738180 | Common:10; Rare:36 | ||||
| chr15:44784333-44784486 | Common:1; Rare:24 |