| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130002452-130002625 | Rare:38 | ||||
| chr11:130003010-130003370 | Common:1; Rare:147 | ||||
| chr11:130069601-130069960 | Common:2; Rare:137 | ||||
| chr11:130070470-130070870 | Common:10; Rare:127 | ||||
| chr11:130314259-130314529 | Common:1; Rare:87 | ||||
| chr11:130314862-130315085 | Common:2; Rare:82 | ||||
| chr11:130448427-130448729 | Common:1; Rare:65 | ||||
| chr11:130892848-130893139 | Common:3; Rare:55 | ||||
| chr11:130916310-130916720 | Common:10; Rare:121 | ||||
| chr11:132943644-132944055 | Common:7; Rare:316 | ||||
| chr11:133956937-133957196 | Common:1; Rare:78 | ||||
| chr11:134068939-134069119 | Rare:97; Clinvar (pathogenic):1 | ||||
| chr11:134126174-134126574 | Common:8; Rare:141 | ||||
| chr11:134223888-134224166 | Common:2; Rare:102 | ||||
| chr11:134224492-134224713 | Common:2; Rare:88 |