| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:48645689-48645938 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr15:48877995-48878276 | Rare:108 | ||||
| chr15:49046321-49046614 | Common:2; Rare:103 | ||||
| chr15:49155525-49155878 | Common:2; Rare:115 | ||||
| chr15:49170105-49170308 | Rare:46 | ||||
| chr15:49423111-49423417 | Common:1; Rare:51 | ||||
| chr15:49620752-49621099 | Common:6; Rare:129 | ||||
| chr15:50354746-50354998 | Rare:70 | ||||
| chr15:50355058-50355493 | Common:3; Rare:168 | ||||
| chr15:50424211-50424466 | Common:2; Rare:96 | ||||
| chr15:50686704-50686914 | Common:4; Rare:87 | ||||
| chr15:50765364-50765521 | Common:1; Rare:52 | ||||
| chr15:50765535-50765766 | Common:2; Rare:79 | ||||
| chr15:50908579-50908790 | Common:2; Rare:91; Clinvar (benign):3 | ||||
| chr15:51751491-51751694 | Common:1; Rare:54 |