| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108121736-108122026 | Common:3; Rare:53 | ||||
| chr11:108122271-108122404 | Rare:30 | ||||
| chr11:108222380-108222439 | Rare:13 | ||||
| chr11:108222522-108223183 | Common:1; Rare:212; Clinvar:9; Clinvar (benign):2 | ||||
| chr11:108223209-108223359 | Rare:43 | ||||
| chr11:108223571-108223799 | Rare:50 | ||||
| chr11:108467121-108467371 | Common:1; Rare:64 | ||||
| chr11:108467374-108467693 | Common:4; Rare:114 | ||||
| chr11:108497637-108498100 | Common:3; Rare:82 | ||||
| chr11:108498248-108498482 | Common:4; Rare:74 | ||||
| chr11:108592813-108593683 | Common:6; Rare:229 | ||||
| chr11:108593717-108593785 | Rare:22 | ||||
| chr11:108664762-108665161 | Common:6; Rare:150 | ||||
| chr11:108665287-108665442 | Rare:42 | ||||
| chr11:108929309-108929670 | Common:1; Rare:63 |