| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40907471-40907638 | Rare:35 | ||||
| chr15:40932207-40932546 | Common:1; Rare:93; Clinvar (pathogenic):1 | ||||
| chr15:40932810-40933077 | Common:1; Rare:53 | ||||
| chr15:40933347-40933459 | Rare:23 | ||||
| chr15:40933498-40934153 | Common:2; Rare:97 | ||||
| chr15:40934160-40934272 | Common:1; Rare:24 | ||||
| chr15:40941824-40942191 | Common:2; Rare:113 | ||||
| chr15:41083977-41084191 | Common:1; Rare:34 | ||||
| chr15:41095598-41095820 | Rare:55 | ||||
| chr15:41249856-41249987 | Common:1; Rare:21 | ||||
| chr15:41283755-41284034 | Common:2; Rare:76 | ||||
| chr15:41296825-41296927 | Rare:14 | ||||
| chr15:41297883-41298163 | Common:1; Rare:44 | ||||
| chr15:41371244-41371644 | Rare:82 | ||||
| chr15:41390752-41390993 | Common:1; Rare:44 |