| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17013842-17013987 | Common:6; Rare:59 | ||||
| chr11:17014235-17014330 | Rare:34 | ||||
| chr11:17077607-17077847 | Common:2; Rare:99 | ||||
| chr11:17207870-17208093 | Common:2; Rare:82 | ||||
| chr11:17276566-17276823 | Common:4; Rare:67; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012913-18013248 | Common:6; Rare:112 | ||||
| chr11:18106039-18106308 | Common:2; Rare:81 | ||||
| chr11:18248618-18248832 | Common:1; Rare:50 | ||||
| chr11:18266008-18266299 | Common:3; Rare:64 | ||||
| chr11:18322119-18322332 | Common:5; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322504-18322616 | Common:2; Rare:51 | ||||
| chr11:18394393-18394633 | Common:1; Rare:95; Clinvar (benign):1 | ||||
| chr11:18526847-18526980 | Rare:66 | ||||
| chr11:18588667-18588975 | Common:4; Rare:89 | ||||
| chr11:18634246-18634590 | Common:3; Rare:121 |