| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520297-14520532 | Rare:82 | ||||
| chr11:14643627-14643810 | Common:1; Rare:70 | ||||
| chr11:16607662-16607845 | Common:1; Rare:26 | ||||
| chr11:16738450-16738844 | Common:3; Rare:95 | ||||
| chr11:16881354-16881547 | Common:2; Rare:35 | ||||
| chr11:17013846-17013987 | Common:6; Rare:59 | ||||
| chr11:17014183-17014337 | Rare:59 | ||||
| chr11:17077608-17077877 | Common:2; Rare:113 | ||||
| chr11:17207900-17208102 | Common:2; Rare:79 | ||||
| chr11:17351637-17351827 | Rare:39 | ||||
| chr11:18106050-18106308 | Common:2; Rare:71 | ||||
| chr11:18322077-18322638 | Common:8; Rare:203; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18394432-18394636 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr11:18526835-18526977 | Rare:70 | ||||
| chr11:18588667-18588905 | Common:2; Rare:81 |