| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31420495-31420763 | Common:4; Rare:90 | ||||
| chr14:31561089-31561450 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32075971-32076326 | Common:2; Rare:92 | ||||
| chr14:32076657-32077063 | Common:3; Rare:118 | ||||
| chr14:34462214-34462541 | Common:1; Rare:113 | ||||
| chr14:34714538-34714759 | Common:3; Rare:82 | ||||
| chr14:34875231-34875404 | Rare:67 | ||||
| chr14:34982372-34982709 | Common:1; Rare:136 | ||||
| chr14:35046105-35046595 | Common:2; Rare:171 | ||||
| chr14:35046668-35046772 | Common:4; Rare:38 | ||||
| chr14:35121955-35122806 | Common:4; Rare:236 | ||||
| chr14:35292242-35292462 | Common:3; Rare:81 | ||||
| chr14:35404423-35404750 | Common:3; Rare:115; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:35826724-35826910 | Common:1; Rare:49 | ||||
| chr14:36320584-36320739 | Common:3; Rare:51 |