| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35138700-35138922 | Common:2; Rare:47 | ||||
| chr11:35138954-35139215 | Common:1; Rare:58 | ||||
| chr11:35525529-35525920 | Common:1; Rare:92 | ||||
| chr11:35943975-35944037 | Common:1; Rare:18 | ||||
| chr11:36510255-36510353 | Rare:28 | ||||
| chr11:43880692-43880868 | Common:1; Rare:38 | ||||
| chr11:46700565-46700818 | Common:1; Rare:64 | ||||
| chr11:46700947-46701113 | Common:1; Rare:61 | ||||
| chr11:46846235-46846422 | Common:1; Rare:55 | ||||
| chr11:47185371-47185651 | Common:2; Rare:55 | ||||
| chr11:47248783-47248957 | Rare:72 | ||||
| chr11:47426402-47426648 | Common:1; Rare:61 | ||||
| chr11:47553071-47553374 | Common:2; Rare:105 | ||||
| chr11:47565511-47565621 | Common:2; Rare:20 | ||||
| chr11:47578958-47579128 | Rare:90; Clinvar:2; Clinvar (pathogenic):1 |