| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95534712-95534808 | Rare:23 | ||||
| chr14:95535343-95535366 | Rare:12 | ||||
| chr14:95686229-95686434 | Common:1; Rare:54 | ||||
| chr14:95714112-95714342 | Common:2; Rare:68 | ||||
| chr14:96363198-96363559 | Common:3; Rare:116 | ||||
| chr14:96391767-96392088 | Common:2; Rare:81 | ||||
| chr14:96502232-96502640 | Common:2; Rare:170 | ||||
| chr14:96797205-96797432 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:99478744-99478813 | Rare:12 | ||||
| chr14:99480728-99481224 | Common:2; Rare:163 | ||||
| chr14:100238550-100238831 | Common:3; Rare:84 | ||||
| chr14:100239681-100239915 | Common:2; Rare:79 | ||||
| chr14:100306306-100306640 | Common:4; Rare:102 | ||||
| chr14:100376240-100376535 | Common:3; Rare:95 | ||||
| chr14:101761444-101761709 | Common:5; Rare:69 |