| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62545627-62545987 | Common:1; Rare:79 | ||||
| chr11:62591495-62591837 | Rare:114 | ||||
| chr11:62601228-62601501 | Common:1; Rare:85 | ||||
| chr11:62611429-62611722 | Rare:81 | ||||
| chr11:62612467-62612679 | Common:4; Rare:59 | ||||
| chr11:62626072-62626582 | Common:1; Rare:142; Clinvar (pathogenic):1 | ||||
| chr11:62653259-62653579 | Common:1; Rare:86 | ||||
| chr11:62665109-62665324 | Common:4; Rare:98 | ||||
| chr11:62678863-62679174 | Rare:104 | ||||
| chr11:62691070-62691387 | Common:1; Rare:113; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr11:62697131-62697173 | Common:1; Rare:9 | ||||
| chr11:62706223-62706406 | Common:3; Rare:75; Clinvar (benign):5 | ||||
| chr11:62727417-62727702 | Rare:114 | ||||
| chr11:62728417-62728538 | Common:1; Rare:71 | ||||
| chr11:62754136-62754290 | Common:1; Rare:39 |