| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105487022-105487205 | Common:1; Rare:47 | ||||
| chr15:22980702-22980776 | Common:3; Rare:29 | ||||
| chr15:23039464-23039720 | Common:1; Rare:117 | ||||
| chr15:23447175-23447443 | Common:2; Rare:78 | ||||
| chr15:23565608-23565680 | Rare:24 | ||||
| chr15:23687234-23687435 | Common:1; Rare:76 | ||||
| chr15:24675623-24675796 | Rare:38 | ||||
| chr15:24823552-24823702 | Common:1; Rare:35 | ||||
| chr15:24954890-24955057 | Rare:82 | ||||
| chr15:25438336-25438628 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr15:25438694-25438859 | Rare:50 | ||||
| chr15:25438984-25439227 | Common:2; Rare:91 | ||||
| chr15:25865145-25865301 | Rare:35 | ||||
| chr15:26629053-26629318 | Common:4; Rare:94 | ||||
| chr15:26790262-26790532 | Common:4; Rare:72 |