| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134223922-134224127 | Common:2; Rare:61 | ||||
| chr11:134224533-134224695 | Rare:61 | ||||
| chr11:134225441-134225475 | Rare:10 | ||||
| chr11:134225479-134225557 | Rare:23 | ||||
| chr11:134253286-134253628 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:134331667-134332037 | Common:10; Rare:85 | ||||
| chr12:203503-203660 | Rare:45 | ||||
| chr12:203684-203973 | Common:5; Rare:76 | ||||
| chr12:211191-211420 | Common:2; Rare:29 | ||||
| chr12:262829-263006 | Rare:31 | ||||
| chr12:388964-389033 | Rare:33 | ||||
| chr12:389196-389400 | Common:1; Rare:81 | ||||
| chr12:389454-389605 | Common:5; Rare:57 | ||||
| chr12:401436-401644 | Rare:58 | ||||
| chr12:610367-610450 | Rare:9 |