| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75660761-75661366 | Common:5; Rare:155 | ||||
| chr14:75661429-75661527 | Common:1; Rare:30 | ||||
| chr14:75985626-75985824 | Rare:80; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr14:76151724-76152064 | Common:1; Rare:109 | ||||
| chr14:76152363-76152630 | Common:3; Rare:55 | ||||
| chr14:76761677-76761760 | Rare:21 | ||||
| chr14:76812779-76813030 | Common:2; Rare:101 | ||||
| chr14:77028412-77028566 | Common:1; Rare:39 | ||||
| chr14:77028584-77028963 | Rare:124 | ||||
| chr14:77097706-77097866 | Rare:45 | ||||
| chr14:77097870-77098348 | Rare:148 | ||||
| chr14:77320407-77320545 | Common:3; Rare:52; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr14:77320811-77321105 | Rare:92; Clinvar:3 | ||||
| chr14:77321187-77321552 | Common:7; Rare:175 | ||||
| chr14:77321601-77321957 | Common:4; Rare:93 |