| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20413844-20414000 | Rare:35 | ||||
| chr14:20454493-20455019 | Common:5; Rare:157 | ||||
| chr14:20455034-20455331 | Common:2; Rare:83 | ||||
| chr14:20455358-20455607 | Rare:61 | ||||
| chr14:20461330-20461674 | Common:1; Rare:104 | ||||
| chr14:20461728-20462085 | Common:3; Rare:84 | ||||
| chr14:20469249-20469565 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:20469650-20469857 | Rare:58 | ||||
| chr14:20469974-20470091 | Rare:19 | ||||
| chr14:20609408-20609690 | Common:5; Rare:79 | ||||
| chr14:20609979-20610155 | Common:2; Rare:71 | ||||
| chr14:20683071-20683666 | Common:9; Rare:202 | ||||
| chr14:20683683-20683702 | Rare:1 | ||||
| chr14:20683707-20684026 | Common:8; Rare:86 | ||||
| chr14:20684124-20684283 | Common:4; Rare:32; Clinvar:2; Clinvar (benign):3 |