| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:90397818-90398010 | Rare:50 | ||||
| chr14:90398029-90398170 | Common:3; Rare:28 | ||||
| chr14:91060080-91060460 | Common:9; Rare:333 | ||||
| chr14:91060493-91060954 | Common:5; Rare:238 | ||||
| chr14:91125300-91125570 | Rare:94 | ||||
| chr14:91253330-91253680 | Common:6; Rare:204 | ||||
| chr14:91280330-91280749 | Common:6; Rare:141 | ||||
| chr14:91283637-91283920 | Common:5; Rare:88 | ||||
| chr14:91290850-91291310 | Common:5; Rare:143 | ||||
| chr14:91417542-91418038 | Common:13; Rare:304; Clinvar (benign):1 | ||||
| chr14:91418046-91418339 | Common:1; Rare:156 | ||||
| chr14:91508553-91509611 | Common:10; Rare:646 | ||||
| chr14:91510148-91510957 | Common:5; Rare:619 | ||||
| chr14:91836186-91836813 | Common:44; Rare:318 | ||||
| chr14:92039215-92039765 | Common:9; Rare:284; Clinvar:1; Clinvar (benign):8 |