| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34631827-34632243 | Common:2; Rare:124 | ||||
| chr11:34916027-34916239 | Common:3; Rare:73; Clinvar (benign):2 | ||||
| chr11:34916276-34916681 | Common:10; Rare:163; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139077-35139181 | Rare:18 | ||||
| chr11:35139652-35139837 | Common:2; Rare:29 | ||||
| chr11:35618090-35618530 | Common:5; Rare:116 | ||||
| chr11:35619147-35619342 | Rare:68 | ||||
| chr11:35662798-35662906 | Common:1; Rare:34 | ||||
| chr11:35943927-35944113 | Common:3; Rare:62 | ||||
| chr11:35944335-35944442 | Rare:24 | ||||
| chr11:36289357-36289556 | Common:2; Rare:72 | ||||
| chr11:36510211-36510428 | Common:1; Rare:81 | ||||
| chr11:36594314-36594585 | Common:2; Rare:51 | ||||
| chr11:43311813-43312090 | Common:2; Rare:90 | ||||
| chr11:43358775-43359001 | Rare:108 |