| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40108837-40109074 | Common:1; Rare:70 | ||||
| chr15:40160891-40161360 | Common:6; Rare:112; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:40307742-40308129 | Common:3; Rare:96 | ||||
| chr15:40382813-40383026 | Common:1; Rare:106 | ||||
| chr15:40405577-40405884 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr15:40440695-40441001 | Rare:83 | ||||
| chr15:40470802-40471056 | Rare:76 | ||||
| chr15:40471515-40471683 | Rare:57; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr15:40564933-40565276 | Common:3; Rare:67 | ||||
| chr15:40569114-40569404 | Common:3; Rare:70 | ||||
| chr15:40569740-40569837 | Common:1; Rare:26 | ||||
| chr15:40593906-40594055 | Common:1; Rare:65 | ||||
| chr15:40594239-40594374 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr15:40694597-40694813 | Rare:60 | ||||
| chr15:40695029-40695251 | Common:2; Rare:71 |