| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108467435-108467629 | Common:4; Rare:81 | ||||
| chr11:108664932-108665142 | Common:3; Rare:78 | ||||
| chr11:110130733-110131032 | Rare:62 | ||||
| chr11:110296610-110296784 | Rare:93; Clinvar:4 | ||||
| chr11:111540577-111540839 | Common:1; Rare:75 | ||||
| chr11:111602160-111602561 | Common:1; Rare:130 | ||||
| chr11:111766360-111766454 | Common:1; Rare:58 | ||||
| chr11:111871273-111871348 | Rare:23 | ||||
| chr11:111871483-111871629 | Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111879154-111879557 | Common:1; Rare:121 | ||||
| chr11:111937059-111937436 | Common:7; Rare:102 | ||||
| chr11:112024909-112025167 | Rare:61; Clinvar:3 | ||||
| chr11:112025301-112025520 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:112073985-112074358 | Common:1; Rare:80 | ||||
| chr11:112086645-112086905 | Rare:115; Clinvar:1 |