| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74019216-74019456 | Common:2; Rare:90 | ||||
| chr14:74302915-74303048 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr14:74493200-74493777 | Common:4; Rare:187; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74713042-74713267 | Rare:114 | ||||
| chr14:74881802-74881982 | Common:1; Rare:83 | ||||
| chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
| chr14:75069387-75069680 | Common:2; Rare:73 | ||||
| chr14:75126954-75127120 | Rare:59 | ||||
| chr14:75176412-75176492 | Rare:18 | ||||
| chr14:75660789-75661003 | Rare:55 | ||||
| chr14:75661165-75661330 | Common:2; Rare:45 | ||||
| chr14:76151786-76151972 | Rare:64 | ||||
| chr14:77097940-77098369 | Rare:139 | ||||
| chr14:77320838-77321127 | Rare:90; Clinvar:1 | ||||
| chr14:77377045-77377410 | Common:2; Rare:107 |