| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:106091578-106091686 | Rare:18 | ||||
| chr11:107017752-107017891 | Common:1; Rare:53 | ||||
| chr11:107457338-107457393 | Rare:13 | ||||
| chr11:107457740-107458014 | Common:5; Rare:96 | ||||
| chr11:107565228-107565582 | Common:1; Rare:68 | ||||
| chr11:107565647-107565810 | Rare:46 | ||||
| chr11:107858125-107858289 | Rare:34 | ||||
| chr11:107858476-107858713 | Common:1; Rare:74 | ||||
| chr11:107858718-107859062 | Common:2; Rare:103 | ||||
| chr11:107859064-107859336 | Rare:50 | ||||
| chr11:107859580-107859825 | Common:1; Rare:51 | ||||
| chr11:108008696-108009019 | Common:1; Rare:87 | ||||
| chr11:108009192-108009401 | Rare:86 | ||||
| chr11:108009647-108009709 | Rare:12 | ||||
| chr11:108121370-108121671 | Common:5; Rare:104; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 |