| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207920-17208078 | Common:1; Rare:61 | ||||
| chr11:17276566-17276827 | Common:4; Rare:67; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17719291-17719572 | Common:5; Rare:63 | ||||
| chr11:18106050-18106308 | Common:2; Rare:71 | ||||
| chr11:18322131-18322312 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322521-18322613 | Common:1; Rare:42 | ||||
| chr11:18526841-18526971 | Rare:65 | ||||
| chr11:18588687-18588827 | Common:1; Rare:41 | ||||
| chr11:20669474-20669652 | Common:1; Rare:82 | ||||
| chr11:26994143-26994168 | Rare:4 | ||||
| chr11:27506749-27506859 | Common:1; Rare:46 | ||||
| chr11:28108120-28108430 | Common:1; Rare:96 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509575-31509784 | Common:1; Rare:65 | ||||
| chr11:32829647-32829953 | Common:4; Rare:63 |