| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24195426-24195756 | Common:1; Rare:77 | ||||
| chr14:24232312-24232638 | Common:8; Rare:78 | ||||
| chr14:34630114-34630295 | Common:5; Rare:82 | ||||
| chr14:35046105-35046452 | Common:2; Rare:115 | ||||
| chr14:35122517-35122570 | Common:1; Rare:18 | ||||
| chr14:35292179-35292463 | Common:4; Rare:104 | ||||
| chr14:39103173-39103298 | Common:1; Rare:34 | ||||
| chr14:44961929-44962243 | Common:3; Rare:87 | ||||
| chr14:49586337-49586692 | Common:1; Rare:186 | ||||
| chr14:49598648-49598946 | Common:1; Rare:115 | ||||
| chr14:49620580-49620786 | Common:2; Rare:78 | ||||
| chr14:49892909-49893104 | Rare:79 | ||||
| chr14:50312100-50312324 | Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50944405-50944573 | Common:4; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51651627-51651973 | Common:4; Rare:97 |