| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93879972-93880189 | Common:2; Rare:47 | ||||
| chr14:94213083-94213321 | Rare:44 | ||||
| chr14:94227111-94227274 | Rare:29 | ||||
| chr14:94599350-94599415 | Rare:11 | ||||
| chr14:94694596-94694784 | Rare:33 | ||||
| chr14:94819710-94819796 | Common:2; Rare:13 | ||||
| chr14:94885620-94885934 | Common:9; Rare:48 | ||||
| chr14:94888156-94888416 | Common:1; Rare:56 | ||||
| chr14:94936632-94936857 | Rare:48 | ||||
| chr14:94937327-94937631 | Common:1; Rare:62 | ||||
| chr14:95096107-95096326 | Common:1; Rare:49; Clinvar:9; Clinvar (benign):12 | ||||
| chr14:95097394-95097684 | Common:3; Rare:61 | ||||
| chr14:95185507-95185670 | Common:1; Rare:24 | ||||
| chr14:95256242-95256413 | Rare:24 | ||||
| chr14:95265620-95265968 | Common:5; Rare:47 |