| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45468298-45468723 | Common:1; Rare:95 | ||||
| chr19:45469237-45469572 | Rare:99 | ||||
| chr19:45470394-45470697 | Common:1; Rare:71 | ||||
| chr19:45478690-45478927 | Common:2; Rare:98 | ||||
| chr19:45479042-45479273 | Common:2; Rare:53 | ||||
| chr19:45496954-45497271 | Common:2; Rare:96 | ||||
| chr19:45507228-45507680 | Common:1; Rare:121 | ||||
| chr19:45584358-45584621 | Common:1; Rare:91; Clinvar:1 | ||||
| chr19:45584739-45585114 | Common:5; Rare:131; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45863071-45863359 | Common:4; Rare:97 | ||||
| chr19:45902594-45902922 | Common:3; Rare:99 | ||||
| chr19:46023051-46023071 | Rare:7 | ||||
| chr19:46346978-46347197 | Common:3; Rare:75 | ||||
| chr19:46413544-46413623 | Rare:28 | ||||
| chr19:46471489-46471690 | Common:5; Rare:80 |