| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74019248-74019436 | Common:1; Rare:74 | ||||
| chr14:74493228-74493781 | Common:4; Rare:178; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74612596-74612818 | Common:1; Rare:64 | ||||
| chr14:74713052-74713207 | Rare:87 | ||||
| chr14:75002600-75002952 | Common:1; Rare:97; Clinvar:2 | ||||
| chr14:75126985-75127104 | Rare:39 | ||||
| chr14:75278358-75278620 | Common:1; Rare:58 | ||||
| chr14:75660809-75661326 | Common:4; Rare:122 | ||||
| chr14:76151778-76151950 | Rare:58 | ||||
| chr14:77320832-77321099 | Rare:83; Clinvar:1 | ||||
| chr14:77377022-77377412 | Common:3; Rare:115 | ||||
| chr14:77457556-77457884 | Common:1; Rare:95 | ||||
| chr14:77708000-77708165 | Common:2; Rare:91 | ||||
| chr14:81220843-81221046 | Common:1; Rare:97 | ||||
| chr14:85530030-85530184 | Common:1; Rare:34 |