| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73787175-73787372 | Common:2; Rare:74 | ||||
| chr14:73851733-73851974 | Common:4; Rare:82 | ||||
| chr14:73886781-73886893 | Common:2; Rare:36 | ||||
| chr14:73950035-73950355 | Common:6; Rare:141; Clinvar (benign):5 | ||||
| chr14:74019248-74019467 | Common:1; Rare:82 | ||||
| chr14:74493270-74493777 | Common:4; Rare:160; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713053-74713210 | Rare:86 | ||||
| chr14:74763174-74763397 | Rare:72 | ||||
| chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
| chr14:75051418-75051530 | Common:2; Rare:32; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75127008-75127110 | Rare:29 | ||||
| chr14:75278948-75279021 | Rare:21 | ||||
| chr14:75280633-75280894 | Common:2; Rare:66 | ||||
| chr14:75660789-75661330 | Common:4; Rare:132 | ||||
| chr14:76151786-76151972 | Rare:64 |