| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130314395-130314519 | Common:1; Rare:41 | ||||
| chr11:130448459-130448680 | Rare:54 | ||||
| chr11:131911364-131911494 | Common:1; Rare:56 | ||||
| chr11:133956961-133957113 | Common:1; Rare:50 | ||||
| chr11:134224533-134224700 | Rare:64 | ||||
| chr11:134253261-134253606 | Common:2; Rare:121; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:389205-389371 | Rare:63 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:610374-610516 | Common:2; Rare:14 | ||||
| chr12:643609-643715 | Rare:20 | ||||
| chr12:907669-907973 | Common:3; Rare:68 | ||||
| chr12:990504-990586 | Common:1; Rare:26 | ||||
| chr12:990741-990873 | Rare:37 | ||||
| chr12:991080-991330 | Common:4; Rare:112 | ||||
| chr12:1690871-1691090 | Common:2; Rare:78 |