| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39587763-39588126 | Common:3; Rare:60; Clinvar:1 | ||||
| chr15:39588718-39589134 | Common:1; Rare:122 | ||||
| chr15:39590842-39591623 | Common:2; Rare:194 | ||||
| chr15:39593144-39593447 | Common:2; Rare:64 | ||||
| chr15:39782797-39782887 | Rare:23 | ||||
| chr15:39934051-39934202 | Common:3; Rare:51 | ||||
| chr15:40038864-40039351 | Common:2; Rare:173 | ||||
| chr15:40106954-40107052 | Rare:11 | ||||
| chr15:40339576-40339862 | Common:1; Rare:80 | ||||
| chr15:40340232-40340450 | Common:2; Rare:41 | ||||
| chr15:40340890-40341028 | Common:2; Rare:51 | ||||
| chr15:40350847-40351083 | Common:1; Rare:51 | ||||
| chr15:40405589-40405861 | Common:2; Rare:85; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40694630-40694742 | Rare:31 | ||||
| chr15:40695050-40695214 | Rare:47 |