| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:96018759-96019159 | Common:11; Rare:96 | ||||
| chr15:96038667-96039067 | Common:9; Rare:157 | ||||
| chr15:96043047-96043226 | Common:2; Rare:31 | ||||
| chr15:96051309-96052297 | Common:2; Rare:198 | ||||
| chr15:96053125-96053525 | Common:2; Rare:144 | ||||
| chr15:96058410-96058840 | Common:6; Rare:135 | ||||
| chr15:96088773-96089173 | Rare:98 | ||||
| chr15:96115142-96115542 | Common:8; Rare:142 | ||||
| chr15:96123650-96124150 | Common:5; Rare:93 | ||||
| chr15:96217703-96218103 | Common:3; Rare:54 | ||||
| chr15:96243600-96243930 | Common:5; Rare:58 | ||||
| chr15:96321507-96322190 | Common:5; Rare:241 | ||||
| chr15:96324571-96325101 | Common:6; Rare:276 | ||||
| chr15:96326476-96327418 | Common:11; Rare:345 | ||||
| chr15:96334582-96334730 | Rare:32; Clinvar (pathogenic):1 |