| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:92748509-92748803 | Rare:72 | ||||
| chr14:92793986-92794437 | Rare:142 | ||||
| chr14:93184829-93185013 | Rare:64 | ||||
| chr14:93206985-93207294 | Common:2; Rare:152 | ||||
| chr14:93430231-93430326 | Rare:17 | ||||
| chr14:93430586-93431000 | Rare:79 | ||||
| chr14:93927138-93927333 | Rare:42 | ||||
| chr14:94026208-94026531 | Common:3; Rare:81 | ||||
| chr14:94081123-94081393 | Common:5; Rare:86 | ||||
| chr14:94129571-94129734 | Common:3; Rare:57 | ||||
| chr14:95157234-95157762 | Common:5; Rare:179; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:95157963-95158043 | Common:1; Rare:19 | ||||
| chr14:95534582-95534672 | Rare:33 | ||||
| chr14:95535368-95535421 | Rare:27; Clinvar (pathogenic):1 | ||||
| chr14:96363333-96363552 | Common:1; Rare:71 |