| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65109419-65109852 | Common:2; Rare:131 | ||||
| chr11:65117658-65117955 | Common:4; Rare:109 | ||||
| chr11:65134480-65134646 | Common:1; Rare:43 | ||||
| chr11:65181009-65181390 | Common:2; Rare:88 | ||||
| chr11:65181488-65181822 | Common:3; Rare:104 | ||||
| chr11:65181833-65181993 | Rare:33 | ||||
| chr11:65261701-65262002 | Common:4; Rare:104 | ||||
| chr11:65293907-65294157 | Common:1; Rare:48 | ||||
| chr11:65314711-65314913 | Rare:71 | ||||
| chr11:65333758-65333911 | Common:1; Rare:76 | ||||
| chr11:65382644-65382723 | Rare:14 | ||||
| chr11:65386507-65386708 | Rare:65 | ||||
| chr11:65525263-65525528 | Rare:57 | ||||
| chr11:65553480-65553802 | Common:2; Rare:72; Clinvar (benign):1 | ||||
| chr11:65570312-65570500 | Rare:73 |