| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17353692-17353789 | Common:4; Rare:32 | ||||
| chr11:17526752-17527025 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:17531291-17531411 | Rare:47; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:28559581-28560014 | Common:3; Rare:80 | ||||
| chr11:28566621-28567020 | Common:5; Rare:70 | ||||
| chr11:28652647-28652715 | Rare:14 | ||||
| chr11:28673794-28674034 | Common:1; Rare:41 | ||||
| chr11:28679850-28680220 | Rare:71 | ||||
| chr11:28702182-28702969 | Common:5; Rare:135 | ||||
| chr11:28702976-28702998 | |||||
| chr11:28703013-28703128 | Rare:26 | ||||
| chr11:28704843-28704972 | Common:1; Rare:26 | ||||
| chr11:28705129-28705328 | Rare:35 | ||||
| chr11:28715692-28715946 | Common:1; Rare:44 | ||||
| chr11:28725857-28726156 | Common:2; Rare:50 |