| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39174890-39175273 | Common:6; Rare:131 | ||||
| chr14:39267081-39267396 | Common:1; Rare:104 | ||||
| chr14:39432420-39432648 | Common:6; Rare:79 | ||||
| chr14:44961903-44962258 | Common:3; Rare:103 | ||||
| chr14:45083981-45084191 | Common:1; Rare:76 | ||||
| chr14:45253088-45253310 | Rare:58 | ||||
| chr14:49586317-49586753 | Common:1; Rare:228; Clinvar (benign):1 | ||||
| chr14:49598912-49598991 | Rare:22 | ||||
| chr14:49620574-49620771 | Common:2; Rare:74 | ||||
| chr14:49892940-49893109 | Rare:69 | ||||
| chr14:50312217-50312374 | Rare:57 | ||||
| chr14:50532494-50532621 | Common:2; Rare:38 | ||||
| chr14:50668329-50668556 | Common:3; Rare:85 | ||||
| chr14:50944410-50944638 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:51240021-51240295 | Common:2; Rare:98 |