| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43370904-43371117 | Common:3; Rare:59 | ||||
| chr15:43493082-43493322 | Common:1; Rare:70 | ||||
| chr15:43510665-43510954 | Rare:91 | ||||
| chr15:43746298-43746479 | Common:1; Rare:73 | ||||
| chr15:43826882-43827035 | Rare:59 | ||||
| chr15:44427560-44427646 | Rare:27 | ||||
| chr15:44536666-44537218 | Common:2; Rare:171 | ||||
| chr15:44663556-44663845 | Rare:143; Clinvar:11; Clinvar (benign):6 | ||||
| chr15:44711363-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45200489-45200655 | Common:1; Rare:46 | ||||
| chr15:45201096-45201133 | Common:1; Rare:18 | ||||
| chr15:45587319-45587461 | Rare:44; Clinvar:4 | ||||
| chr15:48331056-48331137 | Rare:14 | ||||
| chr15:48331359-48331476 | Rare:41 | ||||
| chr15:48878060-48878318 | Rare:98 |