| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35643502-35643707 | Rare:75 | ||||
| chr19:35648075-35648380 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35717410-35717800 | Common:4; Rare:91 | ||||
| chr19:35718000-35718400 | Rare:161 | ||||
| chr19:35740539-35740821 | Common:6; Rare:99 | ||||
| chr19:35744884-35745131 | Common:3; Rare:76 | ||||
| chr19:35745347-35745703 | Rare:108 | ||||
| chr19:35748262-35748600 | Common:3; Rare:96 | ||||
| chr19:35757855-35758207 | Common:2; Rare:105 | ||||
| chr19:35767794-35768194 | Common:9; Rare:206 | ||||
| chr19:35775314-35775611 | Common:1; Rare:82 | ||||
| chr19:35775640-35776060 | Common:4; Rare:86 | ||||
| chr19:35856077-35856373 | Common:1; Rare:64 | ||||
| chr19:35856802-35856990 | Rare:37 | ||||
| chr19:35868468-35868637 | Common:1; Rare:43 |