| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:107457193-107457345 | Common:1; Rare:31 | ||||
| chr11:107457736-107458024 | Common:5; Rare:99 | ||||
| chr11:107565210-107565299 | Common:1; Rare:17 | ||||
| chr11:107565433-107565576 | Rare:33 | ||||
| chr11:107565582-107565839 | Common:2; Rare:68 | ||||
| chr11:107858163-107858266 | Rare:21 | ||||
| chr11:107858702-107859149 | Common:2; Rare:118 | ||||
| chr11:107859162-107859221 | Rare:15 | ||||
| chr11:107928145-107928529 | Common:4; Rare:95 | ||||
| chr11:108008777-108009185 | Common:1; Rare:101 | ||||
| chr11:108009219-108009604 | Common:1; Rare:125 | ||||
| chr11:108009693-108009732 | Rare:13 | ||||
| chr11:108121375-108121672 | Common:5; Rare:102; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108121901-108121969 | Rare:9 | ||||
| chr11:108222495-108222841 | Rare:127 |