| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31420524-31420763 | Common:3; Rare:71 | ||||
| chr14:31561169-31561463 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076272-32076308 | Rare:6 | ||||
| chr14:32076657-32077045 | Common:3; Rare:115 | ||||
| chr14:33950583-33950707 | Rare:37 | ||||
| chr14:34462233-34462548 | Common:1; Rare:104 | ||||
| chr14:34875264-34875404 | Rare:57 | ||||
| chr14:34982508-34982727 | Common:1; Rare:93 | ||||
| chr14:35046130-35046520 | Common:1; Rare:132 | ||||
| chr14:35046533-35046702 | Common:1; Rare:64 | ||||
| chr14:35122470-35122781 | Common:2; Rare:99 | ||||
| chr14:35292159-35292463 | Common:4; Rare:109 | ||||
| chr14:35402774-35403204 | Common:4; Rare:133; Clinvar (benign):4 | ||||
| chr14:35404423-35404804 | Common:3; Rare:129; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:35826724-35826741 | Rare:4 |