| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95535262-95535290 | Common:1; Rare:9; Clinvar (benign):1 | ||||
| chr14:95535595-95535781 | Common:2; Rare:46 | ||||
| chr14:95711367-95711730 | Rare:68 | ||||
| chr14:95711738-95711866 | Common:1; Rare:36 | ||||
| chr14:95711921-95712253 | Common:3; Rare:63 | ||||
| chr14:95713215-95713514 | Common:1; Rare:83 | ||||
| chr14:95713918-95714383 | Common:5; Rare:181 | ||||
| chr14:96363134-96363583 | Common:3; Rare:139 | ||||
| chr14:96364082-96364279 | Common:1; Rare:46 | ||||
| chr14:96391691-96392163 | Common:3; Rare:128 | ||||
| chr14:96501944-96502487 | Common:1; Rare:176 | ||||
| chr14:96502708-96502863 | Common:4; Rare:48 | ||||
| chr14:96797109-96797450 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:99480736-99481041 | Common:2; Rare:119 | ||||
| chr14:99481275-99481504 | Rare:66 |