| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17276557-17276806 | Common:3; Rare:67; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:17719321-17719757 | Common:5; Rare:106 | ||||
| chr11:17719826-17720049 | Rare:83 | ||||
| chr11:18012911-18013246 | Common:6; Rare:111 | ||||
| chr11:18105962-18106312 | Common:4; Rare:117 | ||||
| chr11:18322119-18322312 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322476-18322616 | Common:2; Rare:59 | ||||
| chr11:18394380-18394633 | Common:1; Rare:102; Clinvar (benign):1 | ||||
| chr11:18526841-18527001 | Common:1; Rare:77 | ||||
| chr11:18588667-18588878 | Common:2; Rare:72 | ||||
| chr11:18634313-18634580 | Common:2; Rare:86 | ||||
| chr11:18634805-18634861 | Rare:7 | ||||
| chr11:18698526-18698747 | Common:3; Rare:50 | ||||
| chr11:19116951-19117221 | Common:3; Rare:75 | ||||
| chr11:20387417-20387797 | Common:7; Rare:126 |