| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34916287-34916709 | Common:10; Rare:173; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139018-35139360 | Common:1; Rare:93 | ||||
| chr11:35943987-35944128 | Common:1; Rare:45 | ||||
| chr11:36510229-36510418 | Rare:67 | ||||
| chr11:43358845-43358983 | Rare:65 | ||||
| chr11:43680455-43680822 | Common:1; Rare:102 | ||||
| chr11:43880653-43880915 | Common:2; Rare:73 | ||||
| chr11:44066195-44066335 | Common:1; Rare:33 | ||||
| chr11:45286197-45286440 | Rare:76 | ||||
| chr11:45804987-45805193 | Common:3; Rare:53; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45917824-45918183 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46380739-46381114 | Common:1; Rare:91 | ||||
| chr11:46382168-46382458 | Rare:98 | ||||
| chr11:46617165-46617591 | Common:5; Rare:120 | ||||
| chr11:46700555-46700823 | Common:1; Rare:68 |