| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44663637-44663842 | Rare:86; Clinvar:2 | ||||
| chr15:44711202-44711611 | Rare:105; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45129850-45129996 | Rare:33 | ||||
| chr15:45201108-45201133 | Common:1; Rare:13 | ||||
| chr15:45587093-45587263 | Rare:31 | ||||
| chr15:45587313-45587456 | Rare:43; Clinvar:4 | ||||
| chr15:47717938-47718103 | Common:1; Rare:36 | ||||
| chr15:48331359-48331453 | Rare:32 | ||||
| chr15:48332163-48332247 | Common:2; Rare:32 | ||||
| chr15:48645698-48645950 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr15:48878042-48878733 | Common:1; Rare:238 | ||||
| chr15:49046370-49046622 | Common:2; Rare:87 | ||||
| chr15:49155538-49155846 | Common:2; Rare:102 | ||||
| chr15:49170088-49170269 | Rare:35 | ||||
| chr15:49423076-49423440 | Common:1; Rare:59 |