| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63543312-63543569 | Common:3; Rare:67 | ||||
| chr14:63641823-63642162 | Common:4; Rare:112 | ||||
| chr14:63727999-63728178 | Common:1; Rare:84 | ||||
| chr14:63852896-63853084 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:64387952-64388385 | Common:2; Rare:151 | ||||
| chr14:64465359-64465524 | Common:1; Rare:48 | ||||
| chr14:64503614-64503821 | Common:1; Rare:68 | ||||
| chr14:64504103-64504337 | Common:2; Rare:69 | ||||
| chr14:64504572-64504860 | Rare:86 | ||||
| chr14:64505235-64505381 | Rare:36 | ||||
| chr14:64914183-64914524 | Common:3; Rare:119 | ||||
| chr14:64942673-64943111 | Common:1; Rare:98 | ||||
| chr14:64987097-64987284 | Rare:69 | ||||
| chr14:65411748-65411939 | Common:2; Rare:53 | ||||
| chr14:65412564-65412886 | Common:4; Rare:104 |