| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130314299-130314495 | Common:1; Rare:61 | ||||
| chr11:130448396-130448666 | Rare:64 | ||||
| chr11:130916411-130916636 | Common:6; Rare:74 | ||||
| chr11:131909651-131909924 | Common:2; Rare:46 | ||||
| chr11:131911386-131911444 | Common:1; Rare:23 | ||||
| chr11:133951620-133951742 | Rare:23 | ||||
| chr11:133952014-133952066 | Rare:19 | ||||
| chr11:134223930-134224103 | Common:2; Rare:50 | ||||
| chr11:134224533-134224667 | Rare:48 | ||||
| chr11:134225435-134225532 | Rare:29 | ||||
| chr11:134253286-134253592 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr12:389242-389383 | Rare:53 | ||||
| chr12:389472-389670 | Common:5; Rare:81 | ||||
| chr12:401426-401664 | Common:1; Rare:69 | ||||
| chr12:610367-610466 | Rare:10 |