| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34875296-34875404 | Rare:43 | ||||
| chr14:34982504-34982709 | Common:1; Rare:88 | ||||
| chr14:35046119-35046529 | Common:2; Rare:137 | ||||
| chr14:35122225-35122605 | Common:1; Rare:114 | ||||
| chr14:35292246-35292462 | Common:3; Rare:80 | ||||
| chr14:35826742-35826910 | Common:1; Rare:45 | ||||
| chr14:39114215-39114341 | Common:2; Rare:47 | ||||
| chr14:39175002-39175296 | Common:4; Rare:105 | ||||
| chr14:39267075-39267417 | Common:1; Rare:120 | ||||
| chr14:39432414-39432672 | Common:6; Rare:85 | ||||
| chr14:44961897-44962258 | Common:3; Rare:105 | ||||
| chr14:45083788-45084174 | Common:2; Rare:127 | ||||
| chr14:49586327-49586772 | Common:1; Rare:237; Clinvar (benign):1 | ||||
| chr14:49598684-49599015 | Common:2; Rare:126 | ||||
| chr14:49620564-49620842 | Common:2; Rare:117; Clinvar:3 |