| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95319816-95320158 | Common:5; Rare:79 | ||||
| chr14:95534587-95534692 | Rare:36 | ||||
| chr14:96363272-96363552 | Common:1; Rare:93 | ||||
| chr14:96502301-96502471 | Rare:64 | ||||
| chr14:99480769-99481007 | Common:2; Rare:94 | ||||
| chr14:100376269-100376504 | Common:3; Rare:78 | ||||
| chr14:102086989-102087429 | Common:5; Rare:190 | ||||
| chr14:102139651-102139932 | Rare:99 | ||||
| chr14:102305075-102305337 | Common:1; Rare:80 | ||||
| chr14:102362862-102363098 | Rare:104 | ||||
| chr14:103529058-103529233 | Common:1; Rare:51 | ||||
| chr14:103562624-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
| chr14:103629133-103629419 | Common:2; Rare:112 | ||||
| chr14:103715470-103715859 | Common:1; Rare:125 | ||||
| chr14:103928254-103928465 | Common:2; Rare:70 |