| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39782744-39783044 | Common:2; Rare:177 | ||||
| chr15:39920843-39921110 | Common:10; Rare:232 | ||||
| chr15:39933904-39934292 | Common:12; Rare:306; Clinvar (benign):1 | ||||
| chr15:39976710-39977150 | Common:13; Rare:260; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr15:40038850-40039384 | Common:4; Rare:439 | ||||
| chr15:40106573-40106745 | Common:1; Rare:48 | ||||
| chr15:40108819-40109182 | Common:3; Rare:171 | ||||
| chr15:40160784-40161158 | Common:15; Rare:265 | ||||
| chr15:40238970-40239650 | Common:7; Rare:286 | ||||
| chr15:40252449-40252752 | Common:1; Rare:110 | ||||
| chr15:40282224-40283064 | Rare:415 | ||||
| chr15:40340833-40341073 | Common:6; Rare:128 | ||||
| chr15:40358000-40358510 | Common:13; Rare:214 | ||||
| chr15:40382770-40383075 | Common:1; Rare:145 | ||||
| chr15:40405556-40405884 | Common:6; Rare:276; Clinvar:3; Clinvar (benign):12; Clinvar (pathogenic):10 |