| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20454513-20454657 | Rare:49 | ||||
| chr14:20454772-20455381 | Common:7; Rare:157 | ||||
| chr14:20455496-20455564 | Rare:16 | ||||
| chr14:20459590-20459872 | Common:2; Rare:65 | ||||
| chr14:20460869-20461045 | Common:1; Rare:41 | ||||
| chr14:20461698-20462020 | Common:4; Rare:75 | ||||
| chr14:20684479-20684695 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:21211555-21211866 | Common:3; Rare:81 | ||||
| chr14:21262902-21262942 | Rare:7 | ||||
| chr14:21476837-21477258 | Common:2; Rare:135 | ||||
| chr14:21511252-21511525 | Rare:83 | ||||
| chr14:22589141-22589508 | Common:4; Rare:113 | ||||
| chr14:22766497-22766731 | Common:1; Rare:124 | ||||
| chr14:22829742-22829947 | Common:1; Rare:66 | ||||
| chr14:22871687-22872001 | Rare:78 |