| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49621245-49621311 | Rare:25 | ||||
| chr14:49634594-49634943 | Common:1; Rare:147; Clinvar:14; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:49635113-49635348 | Common:1; Rare:62; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49688005-49688511 | Common:4; Rare:160 | ||||
| chr14:49692966-49693335 | Common:1; Rare:143 | ||||
| chr14:49693347-49693574 | Common:1; Rare:80 | ||||
| chr14:49767300-49767458 | Common:1; Rare:24 | ||||
| chr14:49767483-49767573 | Rare:32 | ||||
| chr14:49767580-49767771 | Common:2; Rare:56 | ||||
| chr14:49767930-49768285 | Common:2; Rare:125 | ||||
| chr14:49768489-49768699 | Rare:82 | ||||
| chr14:49768724-49769077 | Rare:81 | ||||
| chr14:49852423-49852618 | Common:3; Rare:55 | ||||
| chr14:49852658-49852861 | Common:2; Rare:93 | ||||
| chr14:49852990-49853154 | Rare:35 |