| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34539629-34539882 | Common:1; Rare:69 | ||||
| chr14:34982515-34982637 | Common:1; Rare:50 | ||||
| chr14:35046089-35046566 | Common:2; Rare:163 | ||||
| chr14:35121950-35122578 | Common:3; Rare:180 | ||||
| chr14:39170249-39170476 | Common:3; Rare:67 | ||||
| chr14:39267083-39267423 | Common:1; Rare:121 | ||||
| chr14:44961892-44962254 | Common:3; Rare:105 | ||||
| chr14:49586343-49586713 | Common:1; Rare:195 | ||||
| chr14:49598679-49598991 | Common:1; Rare:121 | ||||
| chr14:49620562-49620840 | Common:2; Rare:116; Clinvar:3 | ||||
| chr14:49892903-49893109 | Rare:84 | ||||
| chr14:50312207-50312374 | Rare:64 | ||||
| chr14:50668322-50668556 | Common:3; Rare:86 | ||||
| chr14:50944350-50944638 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51651550-51651960 | Common:4; Rare:109 |