| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18412223-18412445 | Common:4; Rare:68 | ||||
| chr11:18481735-18482012 | Common:1; Rare:58 | ||||
| chr11:18526809-18527001 | Common:1; Rare:89 | ||||
| chr11:18588667-18588961 | Common:4; Rare:87 | ||||
| chr11:18599528-18599834 | Common:1; Rare:50 | ||||
| chr11:18602868-18602981 | Common:3; Rare:22 | ||||
| chr11:18634301-18634590 | Common:3; Rare:97 | ||||
| chr11:18634749-18634836 | Rare:29 | ||||
| chr11:18698665-18698772 | Common:2; Rare:31 | ||||
| chr11:18791731-18791891 | Rare:57 | ||||
| chr11:19148544-19148636 | Common:1; Rare:18 | ||||
| chr11:20363659-20363748 | Common:1; Rare:19 | ||||
| chr11:20387417-20387786 | Common:7; Rare:119 | ||||
| chr11:21283616-21283750 | Common:1; Rare:23 | ||||
| chr11:22625483-22625633 | Rare:76; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 |