| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:23303479-23303775 | Rare:25 | ||||
| chr15:25088711-25088804 | Rare:36 | ||||
| chr15:28589233-28589509 | Common:1; Rare:9 | ||||
| chr15:29730564-29730611 | Rare:9 | ||||
| chr15:31215855-31215929 | Common:1; Rare:20 | ||||
| chr15:32536412-32536754 | Common:2; Rare:38 | ||||
| chr15:39580245-39580441 | Common:1; Rare:54 | ||||
| chr15:39583986-39584422 | Common:1; Rare:119 | ||||
| chr15:43876253-43876343 | Common:1; Rare:15 | ||||
| chr15:48421625-48421983 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:48427760-48428033 | Rare:62; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:51094632-51094976 | Common:8; Rare:93 | ||||
| chr15:51949881-51950142 | Rare:67 | ||||
| chr15:62884009-62884186 | Rare:39 | ||||
| chr15:63049368-63049700 | Common:2; Rare:61 |