| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35179991-35180391 | Common:3; Rare:83 | ||||
| chr11:35663054-35663603 | Rare:195; Clinvar (pathogenic):1 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358794-43359097 | Rare:127 | ||||
| chr11:43880701-43880974 | Common:2; Rare:70 | ||||
| chr11:44066091-44066524 | Common:4; Rare:114 | ||||
| chr11:45146511-45146660 | Common:1; Rare:36 | ||||
| chr11:45665624-45665732 | Rare:18 | ||||
| chr11:46277963-46278208 | Rare:64 | ||||
| chr11:46380549-46381298 | Common:5; Rare:193 | ||||
| chr11:46617112-46617294 | Rare:48 | ||||
| chr11:46700555-46700818 | Common:1; Rare:68 | ||||
| chr11:46700928-46701092 | Common:2; Rare:49 | ||||
| chr11:46846220-46846440 | Common:1; Rare:62 | ||||
| chr11:47214338-47214495 | Common:1; Rare:16 |