| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74398369-74398551 | Common:3; Rare:40 | ||||
| chr11:74467519-74467788 | Common:4; Rare:63 | ||||
| chr11:74493739-74493834 | Rare:36 | ||||
| chr11:74949054-74949397 | Common:6; Rare:107 | ||||
| chr11:75150942-75151157 | Rare:35 | ||||
| chr11:75151227-75151266 | Rare:13 | ||||
| chr11:75351603-75351866 | Common:3; Rare:78 | ||||
| chr11:75525882-75526064 | Common:2; Rare:60 | ||||
| chr11:75562080-75562348 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:75814725-75814911 | Rare:43 | ||||
| chr11:76210759-76211027 | Common:3; Rare:64 | ||||
| chr11:76380750-76381364 | Common:4; Rare:199 | ||||
| chr11:76444592-76445088 | Common:1; Rare:123 | ||||
| chr11:76781562-76781796 | Common:1; Rare:51 | ||||
| chr11:76783035-76783411 | Common:10; Rare:117 |