| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63382060-63382362 | Common:4; Rare:61 | ||||
| chr14:63722108-63722357 | Common:1; Rare:39 | ||||
| chr14:63853985-63854030 | Rare:4 | ||||
| chr14:63870802-63870952 | Common:1; Rare:33 | ||||
| chr14:63940089-63940276 | Common:1; Rare:44 | ||||
| chr14:64415441-64415682 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr14:64501609-64501814 | Common:1; Rare:51 | ||||
| chr14:64531525-64531712 | Common:2; Rare:35 | ||||
| chr14:64716861-64716940 | Common:1; Rare:19 | ||||
| chr14:64731152-64731430 | Rare:90 | ||||
| chr14:64766318-64766347 | Rare:10 | ||||
| chr14:66612482-66612747 | Rare:63 | ||||
| chr14:66663622-66663637 | Common:1; Rare:2 | ||||
| chr14:67312289-67312531 | Common:1; Rare:53 | ||||
| chr14:67380619-67380708 | Rare:24 |