| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:26598017-26598179 | Rare:26 | ||||
| chr14:31207677-31207883 | Common:1; Rare:71 | ||||
| chr14:32076811-32077034 | Common:3; Rare:80 | ||||
| chr14:34462226-34462547 | Common:1; Rare:107 | ||||
| chr14:34982479-34982660 | Common:1; Rare:78 | ||||
| chr14:35046175-35046508 | Common:1; Rare:113 | ||||
| chr14:35121942-35122592 | Common:3; Rare:188 | ||||
| chr14:38256054-38256317 | Common:1; Rare:68 | ||||
| chr14:44961908-44962258 | Common:3; Rare:102 | ||||
| chr14:49598707-49598971 | Common:1; Rare:99 | ||||
| chr14:49620596-49620818 | Common:2; Rare:77; Clinvar:1 | ||||
| chr14:50312224-50312374 | Rare:53 | ||||
| chr14:50532494-50532586 | Common:1; Rare:28 | ||||
| chr14:50944400-50944610 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51651662-51651991 | Common:4; Rare:94 |