| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117327918-117328198 | Common:2; Rare:64 | ||||
| chr11:118401549-118401832 | Common:1; Rare:119 | ||||
| chr11:118565795-118566152 | Common:1; Rare:74 | ||||
| chr11:118607528-118607638 | Common:1; Rare:18 | ||||
| chr11:118790849-118791259 | Rare:116 | ||||
| chr11:118997977-118998193 | Common:4; Rare:68 | ||||
| chr11:119018231-119018830 | Common:13; Rare:227 | ||||
| chr11:119018910-119019309 | Common:4; Rare:159 | ||||
| chr11:119057048-119057470 | Common:3; Rare:161 | ||||
| chr11:119067632-119067829 | Common:3; Rare:64 | ||||
| chr11:119101377-119101616 | Rare:71; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:119101813-119101977 | Rare:46; Clinvar:2 | ||||
| chr11:119121303-119121626 | Common:1; Rare:70 | ||||
| chr11:119206172-119206331 | Common:5; Rare:74; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:119381598-119381838 | Common:1; Rare:54 |