| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:29927352-29927548 | Common:3; Rare:64 | ||||
| chr14:29927779-29928019 | Common:2; Rare:80 | ||||
| chr14:30559055-30559185 | Common:2; Rare:45 | ||||
| chr14:31025395-31025664 | Common:2; Rare:61 | ||||
| chr14:31207596-31207858 | Common:2; Rare:94 | ||||
| chr14:31420520-31420763 | Common:3; Rare:74 | ||||
| chr14:31561374-31561450 | Common:1; Rare:29; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32075971-32076326 | Common:2; Rare:92 | ||||
| chr14:32076691-32077041 | Common:3; Rare:108 | ||||
| chr14:34462214-34462558 | Common:1; Rare:119 | ||||
| chr14:34539629-34539804 | Rare:58 | ||||
| chr14:34982495-34982709 | Common:1; Rare:92 | ||||
| chr14:35046148-35046611 | Common:1; Rare:161 | ||||
| chr14:35046624-35046702 | Common:1; Rare:32 | ||||
| chr14:35121955-35122766 | Common:4; Rare:229 |