| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45147295-45147326 | Rare:14 | ||||
| chr11:45286203-45286413 | Rare:68 | ||||
| chr11:45804993-45805175 | Common:3; Rare:42; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847190-45847514 | Common:2; Rare:137 | ||||
| chr11:45917811-45918180 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46119777-46120089 | Common:3; Rare:74 | ||||
| chr11:46120952-46121037 | Rare:8 | ||||
| chr11:46121054-46121299 | Common:2; Rare:45 | ||||
| chr11:46345339-46345469 | Rare:52 | ||||
| chr11:46380745-46381147 | Common:1; Rare:101 | ||||
| chr11:46617174-46617600 | Common:5; Rare:120 | ||||
| chr11:46700549-46701077 | Common:4; Rare:133 | ||||
| chr11:46846211-46846414 | Common:1; Rare:56 | ||||
| chr11:47176805-47177126 | Common:1; Rare:137 | ||||
| chr11:47183034-47183192 | Rare:35 |