| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91244672-91244817 | Common:2; Rare:25 | ||||
| chr14:91510262-91510713 | Common:1; Rare:156 | ||||
| chr14:92040011-92040181 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92121658-92122005 | Common:4; Rare:120 | ||||
| chr14:92793918-92794456 | Rare:171 | ||||
| chr14:93184845-93184996 | Rare:49 | ||||
| chr14:93207023-93207290 | Common:2; Rare:130 | ||||
| chr14:94081133-94081376 | Common:4; Rare:77 | ||||
| chr14:95157419-95157711 | Common:4; Rare:103 | ||||
| chr14:95534609-95534650 | Rare:10 | ||||
| chr14:96204725-96204920 | Common:4; Rare:78 | ||||
| chr14:96256087-96256242 | Rare:21 | ||||
| chr14:96363283-96363550 | Common:1; Rare:88 | ||||
| chr14:96391793-96392119 | Common:2; Rare:90 | ||||
| chr14:96502327-96502477 | Rare:63 |