| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45178147-45178365 | Common:1; Rare:80 | ||||
| chr19:45178595-45178842 | Common:5; Rare:57; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45179375-45179729 | Common:5; Rare:129; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr19:45251135-45251312 | Common:2; Rare:68 | ||||
| chr19:45370515-45370856 | Common:2; Rare:107; Clinvar:1 | ||||
| chr19:45405952-45406209 | Common:2; Rare:52 | ||||
| chr19:45406307-45406713 | Common:3; Rare:101 | ||||
| chr19:45423462-45424241 | Common:6; Rare:168; Clinvar (benign):1 | ||||
| chr19:45424342-45424570 | Common:3; Rare:29 | ||||
| chr19:45424573-45424619 | Common:1; Rare:8 | ||||
| chr19:45428734-45428823 | Rare:15 | ||||
| chr19:45428911-45428922 | Rare:2 | ||||
| chr19:45450363-45450478 | Rare:20 | ||||
| chr19:45450750-45451035 | Common:4; Rare:51 | ||||
| chr19:45469132-45469527 | Common:2; Rare:128 |