| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40238802-40239268 | Common:2; Rare:91 | ||||
| chr15:40239693-40239877 | Common:1; Rare:27 | ||||
| chr15:40251942-40252295 | Common:2; Rare:66 | ||||
| chr15:40252356-40252703 | Common:1; Rare:128 | ||||
| chr15:40252760-40253264 | Common:2; Rare:146 | ||||
| chr15:40283029-40283094 | Rare:9 | ||||
| chr15:40358074-40358299 | Common:8; Rare:97 | ||||
| chr15:40382586-40383043 | Common:3; Rare:161 | ||||
| chr15:40405613-40405861 | Common:2; Rare:78; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40406056-40406139 | Rare:13 | ||||
| chr15:40464210-40464530 | Common:1; Rare:61 | ||||
| chr15:40564976-40565188 | Common:3; Rare:41 | ||||
| chr15:40569201-40569396 | Common:3; Rare:54 | ||||
| chr15:40593940-40594062 | Rare:41 | ||||
| chr15:40594184-40594388 | Common:1; Rare:48; Clinvar (benign):1 |