| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322489-18322721 | Common:2; Rare:85 | ||||
| chr11:18526880-18526971 | Rare:42 | ||||
| chr11:18588622-18588888 | Common:2; Rare:97 | ||||
| chr11:27506736-27506857 | Common:1; Rare:53 | ||||
| chr11:28108148-28108396 | Common:1; Rare:70 | ||||
| chr11:31369737-31369883 | Rare:45 | ||||
| chr11:31509589-31509790 | Common:1; Rare:64 | ||||
| chr11:33015754-33015895 | Common:1; Rare:53 | ||||
| chr11:33161465-33161624 | Common:5; Rare:42 | ||||
| chr11:34052164-34052312 | Common:2; Rare:68 | ||||
| chr11:34438784-34439009 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr11:34916311-34916578 | Common:8; Rare:113; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:35138954-35139254 | Common:1; Rare:73 | ||||
| chr11:35419037-35419156 | Common:1; Rare:30 | ||||
| chr11:36510249-36510353 | Rare:28 |