| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130003294-130003342 | Rare:26 | ||||
| chr11:130189886-130190137 | Common:2; Rare:75 | ||||
| chr11:130314411-130314509 | Common:1; Rare:29 | ||||
| chr11:130448517-130448652 | Rare:36 | ||||
| chr11:134224539-134224703 | Rare:63 | ||||
| chr11:134253306-134253592 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr12:389205-389383 | Rare:69 | ||||
| chr12:389480-389611 | Common:5; Rare:55 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:643624-643642 | Rare:4 | ||||
| chr12:907772-907953 | Common:1; Rare:47 | ||||
| chr12:914155-914456 | Rare:65; Clinvar:1 | ||||
| chr12:949510-949680 | Common:3; Rare:46 | ||||
| chr12:990452-990567 | Common:1; Rare:32 | ||||
| chr12:991101-991245 | Common:1; Rare:53 |