| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:48878035-48878852 | Common:2; Rare:273 | ||||
| chr15:48963130-48963244 | Common:1; Rare:20 | ||||
| chr15:48963427-48963689 | Common:1; Rare:52 | ||||
| chr15:49046321-49046605 | Common:2; Rare:103 | ||||
| chr15:49046764-49046947 | Rare:38 | ||||
| chr15:49155528-49155845 | Common:2; Rare:108 | ||||
| chr15:49170073-49170315 | Rare:51 | ||||
| chr15:49620752-49621149 | Common:7; Rare:144 | ||||
| chr15:50182338-50182428 | Rare:27 | ||||
| chr15:50354920-50355025 | Rare:23 | ||||
| chr15:50355046-50355531 | Common:3; Rare:196 | ||||
| chr15:50424138-50424568 | Common:2; Rare:147 | ||||
| chr15:50686652-50686962 | Common:5; Rare:120 | ||||
| chr15:50765537-50765766 | Common:2; Rare:78 | ||||
| chr15:50908595-50908772 | Common:1; Rare:72; Clinvar (benign):2 |