| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38907823-38908064 | Common:3; Rare:58 | ||||
| chr20:39588187-39588613 | Common:5; Rare:94 | ||||
| chr20:40989854-40990152 | Common:1; Rare:58 | ||||
| chr20:41005365-41005627 | Rare:47 | ||||
| chr20:41029391-41029458 | Rare:22 | ||||
| chr20:41029786-41029954 | Rare:34 | ||||
| chr20:41030355-41030573 | Common:1; Rare:29 | ||||
| chr20:41030864-41031138 | Common:1; Rare:52 | ||||
| chr20:41081137-41081268 | Rare:24 | ||||
| chr20:41084458-41084668 | Rare:45 | ||||
| chr20:41113733-41114151 | Common:2; Rare:95 | ||||
| chr20:41116094-41116329 | Common:1; Rare:38; Clinvar (pathogenic):1 | ||||
| chr20:41139618-41139764 | Rare:25 | ||||
| chr20:41162062-41162208 | Rare:18 | ||||
| chr20:41196806-41197094 | Rare:53 |