| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24271453-24271606 | Common:1; Rare:44 | ||||
| chr14:24299659-24299907 | Common:4; Rare:79 | ||||
| chr14:24398731-24399068 | Common:4; Rare:81 | ||||
| chr14:24442747-24443043 | Common:5; Rare:83 | ||||
| chr14:30559050-30559191 | Common:2; Rare:49 | ||||
| chr14:30622190-30622344 | Rare:55 | ||||
| chr14:31025375-31025662 | Common:2; Rare:65 | ||||
| chr14:31207655-31207946 | Common:2; Rare:104 | ||||
| chr14:31420547-31420763 | Common:2; Rare:63 | ||||
| chr14:31561089-31561450 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076657-32077041 | Common:3; Rare:115 | ||||
| chr14:34462219-34462558 | Common:1; Rare:117 | ||||
| chr14:34539636-34539856 | Rare:63 | ||||
| chr14:34629951-34630268 | Common:5; Rare:129 | ||||
| chr14:34875258-34875450 | Rare:76 |