| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31943001-31943237 | Rare:50 | ||||
| chr11:32032444-32032844 | Common:3; Rare:121 | ||||
| chr11:32033040-32033590 | Common:1; Rare:104 | ||||
| chr11:32087021-32087970 | Common:4; Rare:276 | ||||
| chr11:32088190-32088764 | Common:4; Rare:211 | ||||
| chr11:32092715-32093115 | Common:3; Rare:79 | ||||
| chr11:32105987-32106267 | Common:4; Rare:112 | ||||
| chr11:32107735-32107991 | Common:1; Rare:44 | ||||
| chr11:32153730-32154060 | Common:5; Rare:81 | ||||
| chr11:32154180-32154690 | Common:3; Rare:84 | ||||
| chr11:32184839-32184947 | Common:1; Rare:14 | ||||
| chr11:32396370-32396790 | Common:3; Rare:85; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr11:32420777-32421177 | Common:3; Rare:87 | ||||
| chr11:32775810-32776180 | Common:1; Rare:68 | ||||
| chr11:32821950-32822290 | Common:2; Rare:39 |