| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45150978-45151208 | Common:1; Rare:61 | ||||
| chr15:45160710-45160858 | Common:1; Rare:41 | ||||
| chr15:45162539-45162639 | Common:1; Rare:13 | ||||
| chr15:45279215-45279439 | Common:1; Rare:89 | ||||
| chr15:45464056-45464357 | Rare:46 | ||||
| chr15:48335981-48336087 | Common:1; Rare:37 | ||||
| chr15:48487088-48487332 | Common:2; Rare:68; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr15:51094618-51094988 | Common:8; Rare:100 | ||||
| chr15:51941706-51941974 | Common:2; Rare:44 | ||||
| chr15:51943513-51943826 | Common:2; Rare:46 | ||||
| chr15:51947357-51947604 | Rare:42 | ||||
| chr15:52221193-52221340 | Common:1; Rare:36 | ||||
| chr15:52289705-52289814 | Common:1; Rare:20 | ||||
| chr15:57306724-57306883 | Rare:36 | ||||
| chr15:57518192-57518485 | Common:1; Rare:70 |