| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:92039354-92039561 | Rare:50 | ||||
| chr14:92039619-92039835 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:92040013-92040192 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92121642-92122229 | Common:5; Rare:183 | ||||
| chr14:93184845-93185027 | Rare:64 | ||||
| chr14:93206983-93207426 | Common:3; Rare:192 | ||||
| chr14:93333008-93333177 | Common:1; Rare:65 | ||||
| chr14:93976548-93976860 | Rare:61 | ||||
| chr14:94081127-94081414 | Common:5; Rare:86 | ||||
| chr14:95157484-95157711 | Common:2; Rare:80 | ||||
| chr14:95534557-95534701 | Rare:59 | ||||
| chr14:95534730-95535026 | Common:3; Rare:79 | ||||
| chr14:96204653-96204939 | Common:4; Rare:115 | ||||
| chr14:96255531-96256042 | Rare:87 | ||||
| chr14:96256100-96256543 | Common:3; Rare:83 |