| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:92040019-92040181 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121656-92121990 | Common:5; Rare:109 | ||||
| chr14:93184872-93185013 | Rare:46 | ||||
| chr14:93206991-93207284 | Common:2; Rare:145 | ||||
| chr14:93976556-93976674 | Rare:26 | ||||
| chr14:93976730-93976865 | Rare:20 | ||||
| chr14:94081141-94081333 | Common:4; Rare:63 | ||||
| chr14:95157424-95157716 | Common:4; Rare:105 | ||||
| chr14:95533571-95533682 | Common:1; Rare:46 | ||||
| chr14:95534609-95534705 | Rare:28 | ||||
| chr14:96204726-96204847 | Common:1; Rare:34 | ||||
| chr14:96363377-96363552 | Common:1; Rare:60 | ||||
| chr14:96502261-96502446 | Common:1; Rare:73 | ||||
| chr14:99480776-99481013 | Common:2; Rare:93 | ||||
| chr14:99737565-99737785 | Common:2; Rare:56 |