| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34539653-34539896 | Common:1; Rare:62 | ||||
| chr14:34630049-34630256 | Common:5; Rare:98 | ||||
| chr14:34713482-34713837 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:34875242-34875281 | Rare:13 | ||||
| chr14:34875313-34875381 | Rare:28 | ||||
| chr14:34982508-34982593 | Common:1; Rare:36 | ||||
| chr14:35046119-35046554 | Common:2; Rare:147 | ||||
| chr14:35121950-35122633 | Common:3; Rare:195 | ||||
| chr14:35292179-35292457 | Common:4; Rare:101 | ||||
| chr14:35826702-35826910 | Common:1; Rare:56 | ||||
| chr14:36320585-36320817 | Common:3; Rare:68 | ||||
| chr14:39267081-39267396 | Common:1; Rare:104 | ||||
| chr14:39432444-39432612 | Common:6; Rare:57 | ||||
| chr14:44961903-44962257 | Common:3; Rare:102 | ||||
| chr14:45253161-45253279 | Rare:29 |