| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77761124-77761396 | Common:2; Rare:82 | ||||
| chr14:81220871-81221170 | Common:1; Rare:135 | ||||
| chr14:85530033-85530148 | Common:1; Rare:26 | ||||
| chr14:89954716-89954968 | Rare:68 | ||||
| chr14:90396896-90397106 | Common:2; Rare:109 | ||||
| chr14:92040019-92040124 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121667-92121973 | Common:4; Rare:103 | ||||
| chr14:93184876-93184971 | Rare:29 | ||||
| chr14:93207011-93207284 | Common:2; Rare:135 | ||||
| chr14:94081133-94081387 | Common:4; Rare:79 | ||||
| chr14:95534616-95534672 | Rare:16 | ||||
| chr14:96363327-96363552 | Common:1; Rare:73 | ||||
| chr14:96502251-96502446 | Common:1; Rare:77 | ||||
| chr14:100375433-100375755 | Common:2; Rare:49 | ||||
| chr14:100376269-100376507 | Common:3; Rare:78 |