| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34101612-34102123 | Common:2; Rare:128 | ||||
| chr15:34224946-34225198 | Rare:88 | ||||
| chr15:34582754-34582903 | Rare:45 | ||||
| chr15:34588443-34588561 | Rare:34 | ||||
| chr15:35546128-35546280 | Common:1; Rare:55 | ||||
| chr15:36579518-36579808 | Common:4; Rare:80 | ||||
| chr15:37093458-37093744 | Rare:58; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:37095945-37096209 | Common:2; Rare:59 | ||||
| chr15:37096504-37096646 | Rare:25 | ||||
| chr15:37097578-37097835 | Rare:43 | ||||
| chr15:37098195-37098344 | Common:2; Rare:38 | ||||
| chr15:37098623-37098806 | Rare:40 | ||||
| chr15:37099182-37099274 | Rare:24 | ||||
| chr15:37099646-37099783 | Rare:26 | ||||
| chr15:37099848-37100811 | Common:1; Rare:243 |