| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18634535-18634916 | Common:5; Rare:98 | ||||
| chr11:18698681-18698785 | Common:3; Rare:29 | ||||
| chr11:18706375-18706495 | Rare:19 | ||||
| chr11:19240597-19240695 | Rare:18 | ||||
| chr11:19240866-19241135 | Rare:83 | ||||
| chr11:19241593-19241885 | Common:1; Rare:82 | ||||
| chr11:19712611-19712837 | Common:2; Rare:88 | ||||
| chr11:20363619-20363832 | Common:4; Rare:41 | ||||
| chr11:20364026-20364214 | Common:6; Rare:42 | ||||
| chr11:20387169-20387326 | Common:1; Rare:42 | ||||
| chr11:20387337-20387779 | Common:9; Rare:135 | ||||
| chr11:22192897-22193097 | Rare:44 | ||||
| chr11:22625127-22625309 | Common:2; Rare:75; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:22625375-22625649 | Common:3; Rare:131; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr11:22625769-22625970 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 |