| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108009069-108009237 | Rare:38 | ||||
| chr11:108009284-108009349 | Rare:34 | ||||
| chr11:108222575-108223128 | Common:1; Rare:179; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108467502-108467638 | Common:3; Rare:51 | ||||
| chr11:111766348-111766417 | Rare:38 | ||||
| chr11:111871259-111871330 | Rare:16 | ||||
| chr11:111878673-111878964 | Common:2; Rare:79 | ||||
| chr11:111879154-111879548 | Common:1; Rare:119 | ||||
| chr11:111912730-111912812 | Rare:12 | ||||
| chr11:111913128-111913270 | Rare:40 | ||||
| chr11:112073987-112074363 | Common:1; Rare:81 | ||||
| chr11:112086697-112086917 | Rare:98; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112226304-112226446 | Rare:65 | ||||
| chr11:113314427-113314602 | Rare:62 | ||||
| chr11:113875493-113875781 | Common:4; Rare:106 |