| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:30622194-30622362 | Common:1; Rare:70 | ||||
| chr14:31207611-31207883 | Common:2; Rare:96 | ||||
| chr14:31420528-31420777 | Common:4; Rare:73 | ||||
| chr14:31457360-31457569 | Common:2; Rare:74 | ||||
| chr14:31561089-31561450 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076608-32077041 | Common:3; Rare:126 | ||||
| chr14:34462226-34462575 | Common:1; Rare:120 | ||||
| chr14:34539599-34539855 | Rare:79 | ||||
| chr14:34630072-34630260 | Common:5; Rare:89 | ||||
| chr14:34714551-34714912 | Common:5; Rare:130 | ||||
| chr14:34875249-34875381 | Rare:52 | ||||
| chr14:34982372-34982690 | Common:1; Rare:125 | ||||
| chr14:35046055-35046574 | Common:2; Rare:171 | ||||
| chr14:35122239-35122311 | Rare:20 | ||||
| chr14:35122429-35122787 | Common:2; Rare:108 |