| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31457314-31457584 | Common:2; Rare:97 | ||||
| chr14:31561366-31561481 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076651-32077051 | Common:3; Rare:118 | ||||
| chr14:32329211-32329382 | Rare:27 | ||||
| chr14:33951074-33951213 | Common:1; Rare:48 | ||||
| chr14:34462214-34462621 | Common:1; Rare:136 | ||||
| chr14:34539537-34539856 | Rare:96 | ||||
| chr14:34629951-34630266 | Common:5; Rare:129 | ||||
| chr14:34714531-34714781 | Common:3; Rare:92 | ||||
| chr14:34874813-34875480 | Common:5; Rare:229 | ||||
| chr14:34982372-34982709 | Common:1; Rare:136 | ||||
| chr14:35046079-35046535 | Common:2; Rare:153 | ||||
| chr14:35122066-35122781 | Common:3; Rare:193 | ||||
| chr14:35292179-35292620 | Common:5; Rare:140; Clinvar:1 | ||||
| chr14:35404627-35404905 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):2 |