| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:48811056-48811346 | Rare:74; Clinvar:2 | ||||
| chr15:48878004-48878420 | Rare:157 | ||||
| chr15:49046347-49046668 | Common:2; Rare:112 | ||||
| chr15:49155550-49155838 | Common:2; Rare:96 | ||||
| chr15:49169971-49170306 | Rare:81 | ||||
| chr15:49620810-49621105 | Common:6; Rare:113 | ||||
| chr15:50354885-50355004 | Rare:17 | ||||
| chr15:50355074-50355513 | Common:3; Rare:176 | ||||
| chr15:50424316-50424466 | Common:1; Rare:66 | ||||
| chr15:50686736-50686914 | Common:3; Rare:78 | ||||
| chr15:50765576-50765756 | Common:2; Rare:62 | ||||
| chr15:50908573-50908765 | Common:2; Rare:79; Clinvar (benign):2 | ||||
| chr15:51622757-51623071 | Common:3; Rare:108 | ||||
| chr15:51681405-51681773 | Common:2; Rare:98 | ||||
| chr15:51751465-51751711 | Common:1; Rare:60 |