| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40807450-40807761 | Common:4; Rare:104 | ||||
| chr15:40953181-40953475 | Common:1; Rare:79 | ||||
| chr15:41115982-41116148 | Rare:48 | ||||
| chr15:41416982-41417202 | Common:3; Rare:98 | ||||
| chr15:41660309-41660440 | Rare:35 | ||||
| chr15:42273400-42273535 | Rare:51 | ||||
| chr15:42548733-42548875 | Common:1; Rare:83 | ||||
| chr15:43106028-43106234 | Rare:66 | ||||
| chr15:43330543-43330700 | Rare:59 | ||||
| chr15:43826870-43827007 | Rare:48 | ||||
| chr15:44536855-44537194 | Common:1; Rare:119 | ||||
| chr15:44711355-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45200496-45200656 | Common:1; Rare:44 | ||||
| chr15:45201111-45201135 | Common:1; Rare:11 | ||||
| chr15:45587324-45587475 | Rare:45; Clinvar:3 |