| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45340574-45340823 | Common:2; Rare:74 | ||||
| chr19:45370151-45370205 | Rare:23; Clinvar:2 | ||||
| chr19:45370506-45370850 | Common:2; Rare:112; Clinvar:1 | ||||
| chr19:45371024-45371038 | Rare:1 | ||||
| chr19:45404986-45405263 | Common:1; Rare:55 | ||||
| chr19:45405516-45405642 | Rare:24 | ||||
| chr19:45405729-45405915 | Common:2; Rare:37 | ||||
| chr19:45405981-45406209 | Common:2; Rare:47 | ||||
| chr19:45406302-45406712 | Common:3; Rare:101 | ||||
| chr19:45423465-45423680 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chr19:45423696-45424111 | Common:4; Rare:90 | ||||
| chr19:45424332-45424523 | Common:3; Rare:23 | ||||
| chr19:45450157-45450267 | Common:2; Rare:21 | ||||
| chr19:45450355-45450535 | Rare:32 | ||||
| chr19:45450745-45451092 | Common:4; Rare:62 |