| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43464096-43464292 | Common:4; Rare:39 | ||||
| chr19:43504029-43504562 | Common:7; Rare:143 | ||||
| chr19:43504658-43504866 | Common:1; Rare:46 | ||||
| chr19:43525548-43525825 | Common:1; Rare:40 | ||||
| chr19:43527145-43527434 | Common:6; Rare:99; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43533095-43533583 | Common:3; Rare:145 | ||||
| chr19:43575447-43575837 | Common:3; Rare:103 | ||||
| chr19:43595218-43595352 | Rare:40 | ||||
| chr19:43595971-43596686 | Common:5; Rare:217 | ||||
| chr19:43618955-43619174 | Rare:44 | ||||
| chr19:43619190-43619427 | Rare:51 | ||||
| chr19:43619434-43619836 | Common:3; Rare:116 | ||||
| chr19:43619858-43620128 | Common:1; Rare:75 | ||||
| chr19:43639765-43639970 | Common:1; Rare:70 | ||||
| chr19:43668318-43668459 | Rare:35 |