| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95534534-95534694 | Common:3; Rare:128 | ||||
| chr14:95534717-95535096 | Common:8; Rare:239; Clinvar (benign):8 | ||||
| chr14:96363271-96363559 | Common:2; Rare:182 | ||||
| chr14:96502232-96502590 | Common:3; Rare:257 | ||||
| chr14:99480707-99481160 | Common:4; Rare:251 | ||||
| chr14:99604164-99604517 | Common:6; Rare:160 | ||||
| chr14:100238568-100238956 | Common:4; Rare:230 | ||||
| chr14:100239047-100239257 | Common:1; Rare:87 | ||||
| chr14:100239345-100240029 | Common:7; Rare:405 | ||||
| chr14:100306360-100306790 | Common:7; Rare:236 | ||||
| chr14:100375434-100375689 | Common:2; Rare:59 | ||||
| chr14:100376210-100376548 | Common:6; Rare:188 | ||||
| chr14:100726695-100727094 | Common:2; Rare:171 | ||||
| chr14:101809865-101810320 | Rare:185 | ||||
| chr14:101964321-101964642 | Common:5; Rare:175; Clinvar:2; Clinvar (benign):1 |