| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43876253-43876485 | Common:2; Rare:28 | ||||
| chr15:44813342-44813496 | Rare:29 | ||||
| chr15:48782835-48783172 | Common:2; Rare:67 | ||||
| chr15:50244990-50245091 | Rare:16 | ||||
| chr15:51094631-51094988 | Common:8; Rare:95 | ||||
| chr15:52785133-52785402 | Common:1; Rare:57 | ||||
| chr15:52803485-52803687 | Common:1; Rare:28 | ||||
| chr15:52804490-52804571 | Common:1; Rare:28 | ||||
| chr15:58330111-58330299 | Common:1; Rare:43 | ||||
| chr15:58432528-58432809 | Common:2; Rare:51 | ||||
| chr15:61402245-61402621 | Common:3; Rare:78 | ||||
| chr15:61403938-61404202 | Common:4; Rare:54 | ||||
| chr15:61502000-61502183 | Rare:40 | ||||
| chr15:61715146-61715259 | Common:1; Rare:20 | ||||
| chr15:64160102-64160498 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |