| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63641804-63642089 | Common:4; Rare:89 | ||||
| chr14:63728011-63728134 | Common:1; Rare:56 | ||||
| chr14:63852849-63853070 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:64387930-64388418 | Common:2; Rare:167 | ||||
| chr14:64503597-64503899 | Common:2; Rare:115 | ||||
| chr14:64504557-64504858 | Rare:92 | ||||
| chr14:64822920-64822965 | Rare:9 | ||||
| chr14:64879790-64880130 | Common:2; Rare:82 | ||||
| chr14:64942682-64943049 | Common:1; Rare:86 | ||||
| chr14:64972144-64972403 | Common:5; Rare:72 | ||||
| chr14:64987097-64987262 | Rare:64 | ||||
| chr14:65102131-65102427 | Common:1; Rare:94; Clinvar:4; Clinvar (benign):5 | ||||
| chr14:65102456-65102833 | Common:7; Rare:101; Clinvar:1 | ||||
| chr14:66507792-66508232 | Rare:185 | ||||
| chr14:66508379-66508537 | Rare:55 |