| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:106077263-106077834 | Common:6; Rare:442 | ||||
| chr11:107017565-107017827 | Common:4; Rare:67 | ||||
| chr11:107018494-107018684 | Common:4; Rare:46 | ||||
| chr11:107457728-107458006 | Common:7; Rare:161 | ||||
| chr11:107564980-107565610 | Common:2; Rare:141 | ||||
| chr11:107565644-107565849 | Common:2; Rare:82 | ||||
| chr11:107590800-107591510 | Common:4; Rare:186 | ||||
| chr11:107858713-107859120 | Common:4; Rare:172 | ||||
| chr11:107859080-107859420 | Rare:159 | ||||
| chr11:108008797-108009038 | Common:2; Rare:118 | ||||
| chr11:108009231-108009362 | Rare:144 | ||||
| chr11:108121356-108121660 | Common:14; Rare:245; Clinvar:3; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:108222461-108223460 | Common:3; Rare:564; Clinvar:14; Clinvar (benign):8 | ||||
| chr11:108467349-108467720 | Common:9; Rare:281 | ||||
| chr11:108497720-108498110 | Common:3; Rare:82 |