| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:94081133-94081319 | Common:4; Rare:63 | ||||
| chr14:94129571-94129730 | Common:3; Rare:53 | ||||
| chr14:95157422-95157707 | Common:4; Rare:100 | ||||
| chr14:95534609-95534664 | Rare:13 | ||||
| chr14:96363283-96363552 | Common:1; Rare:90 | ||||
| chr14:96502301-96502592 | Common:1; Rare:126 | ||||
| chr14:100238535-100238790 | Common:3; Rare:76 | ||||
| chr14:100376259-100376511 | Common:3; Rare:80 | ||||
| chr14:101964370-101964674 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102086978-102087409 | Common:5; Rare:184 | ||||
| chr14:102139644-102139923 | Rare:99 | ||||
| chr14:102362862-102363092 | Rare:103 | ||||
| chr14:103333951-103334252 | Common:2; Rare:123 | ||||
| chr14:103334628-103334812 | Common:1; Rare:82 | ||||
| chr14:103562623-103563048 | Common:8; Rare:166; Clinvar (benign):5 |