| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40807421-40807767 | Common:4; Rare:117 | ||||
| chr15:40894213-40894477 | Rare:81 | ||||
| chr15:41417017-41417178 | Common:1; Rare:71 | ||||
| chr15:42273400-42273615 | Rare:78 | ||||
| chr15:42548725-42548890 | Common:2; Rare:92 | ||||
| chr15:43330019-43330362 | Common:2; Rare:185 | ||||
| chr15:43330543-43330738 | Common:1; Rare:72 | ||||
| chr15:43371030-43371160 | Common:1; Rare:29 | ||||
| chr15:43824623-43824802 | Common:2; Rare:47 | ||||
| chr15:43826904-43827044 | Rare:60 | ||||
| chr15:44427541-44427653 | Rare:30 | ||||
| chr15:44536863-44537197 | Common:1; Rare:118 | ||||
| chr15:44711297-44711611 | Rare:92; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45201115-45201133 | Common:1; Rare:10 | ||||
| chr15:45587102-45587456 | Common:1; Rare:86; Clinvar:6; Clinvar (benign):1 |