| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42548729-42548959 | Common:2; Rare:113 | ||||
| chr15:42575457-42575672 | Common:1; Rare:71 | ||||
| chr15:43105973-43106175 | Rare:68 | ||||
| chr15:43185220-43185489 | Rare:81 | ||||
| chr15:43330511-43330737 | Common:1; Rare:84 | ||||
| chr15:43371017-43371109 | Rare:20 | ||||
| chr15:43510670-43510954 | Rare:91 | ||||
| chr15:43746267-43746463 | Common:1; Rare:73 | ||||
| chr15:43824493-43824811 | Common:2; Rare:96 | ||||
| chr15:44288625-44288971 | Common:1; Rare:101 | ||||
| chr15:44427472-44427789 | Common:1; Rare:79 | ||||
| chr15:44536858-44537236 | Common:3; Rare:140 | ||||
| chr15:44711321-44711613 | Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45201108-45201133 | Common:1; Rare:13 | ||||
| chr15:45402197-45402425 | Common:6; Rare:76 |