| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24242596-24242770 | Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24271481-24271692 | Common:2; Rare:59 | ||||
| chr14:24299749-24299879 | Common:1; Rare:38 | ||||
| chr14:24442761-24443023 | Common:5; Rare:75 | ||||
| chr14:30559047-30559211 | Common:2; Rare:63 | ||||
| chr14:31207640-31207902 | Common:2; Rare:92 | ||||
| chr14:31561294-31561442 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076844-32077051 | Common:3; Rare:76 | ||||
| chr14:34462233-34462530 | Common:1; Rare:99 | ||||
| chr14:34630093-34630224 | Common:5; Rare:65 | ||||
| chr14:34875302-34875594 | Common:1; Rare:99 | ||||
| chr14:34982508-34982696 | Common:1; Rare:79 | ||||
| chr14:35046119-35046466 | Common:2; Rare:115 | ||||
| chr14:35121955-35122609 | Common:3; Rare:187 | ||||
| chr14:35122652-35122772 | Common:1; Rare:34 |