| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67483248-67483648 | Common:3; Rare:159; Clinvar (benign):1 | ||||
| chr11:67504280-67504718 | Common:6; Rare:263 | ||||
| chr11:67505216-67505616 | Rare:197 | ||||
| chr11:67508050-67508505 | Common:6; Rare:464 | ||||
| chr11:67508537-67508937 | Common:19; Rare:429 | ||||
| chr11:67583400-67583970 | Common:24; Rare:634 | ||||
| chr11:67584204-67584687 | Common:8; Rare:424 | ||||
| chr11:67584702-67585278 | Common:4; Rare:181; Clinvar:1 | ||||
| chr11:67605977-67606742 | Common:8; Rare:244 | ||||
| chr11:67606672-67607072 | Common:4; Rare:317; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr11:67629170-67630655 | Common:39; Rare:1025 | ||||
| chr11:68003950-68004390 | Common:4; Rare:321; Clinvar (benign):1 | ||||
| chr11:68009508-68009831 | Common:4; Rare:60 | ||||
| chr11:68009982-68010443 | Common:5; Rare:347 | ||||
| chr11:68010420-68010760 | Common:1; Rare:57 |