| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74881795-74881959 | Common:1; Rare:70 | ||||
| chr14:75002658-75002968 | Common:1; Rare:95; Clinvar:2 | ||||
| chr14:75051416-75051514 | Common:1; Rare:29; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:75069377-75069732 | Common:2; Rare:86 | ||||
| chr14:75126891-75127137 | Common:1; Rare:88 | ||||
| chr14:75279440-75279660 | Rare:49 | ||||
| chr14:75427625-75427768 | Rare:36 | ||||
| chr14:75427850-75428188 | Rare:75 | ||||
| chr14:75660821-75661373 | Common:5; Rare:138 | ||||
| chr14:76762648-76762966 | Rare:104 | ||||
| chr14:77098001-77098412 | Rare:122 | ||||
| chr14:77320854-77321056 | Rare:59; Clinvar:1 | ||||
| chr14:77377045-77377414 | Common:2; Rare:108 | ||||
| chr14:77457524-77457886 | Common:2; Rare:112 | ||||
| chr14:77616755-77617083 | Common:1; Rare:72; Clinvar (benign):2 |