| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134224435-134224717 | Common:2; Rare:114 | ||||
| chr11:134225413-134225639 | Rare:68 | ||||
| chr11:134252957-134253012 | Common:1; Rare:10 | ||||
| chr11:134253285-134253617 | Common:2; Rare:124; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134276155-134276383 | Common:3; Rare:48 | ||||
| chr11:134331680-134332093 | Common:10; Rare:101 | ||||
| chr11:134332315-134332325 | Rare:3 | ||||
| chr11:134332340-134332417 | Rare:25 | ||||
| chr12:388485-388712 | Common:1; Rare:52 | ||||
| chr12:389010-389042 | Rare:12 | ||||
| chr12:389191-389406 | Common:1; Rare:88 | ||||
| chr12:389438-389730 | Common:7; Rare:115 | ||||
| chr12:401426-401786 | Common:1; Rare:94 | ||||
| chr12:401789-401918 | Rare:24 | ||||
| chr12:459853-460172 | Common:3; Rare:102 |