| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35139413-35139764 | Common:3; Rare:81 | ||||
| chr19:35155148-35155230 | Rare:16 | ||||
| chr19:35155348-35155590 | Rare:65 | ||||
| chr19:35248848-35249050 | Common:1; Rare:94 | ||||
| chr19:35266848-35267141 | Common:2; Rare:102 | ||||
| chr19:35268395-35268537 | Rare:21 | ||||
| chr19:35268979-35269162 | Common:1; Rare:24 | ||||
| chr19:35329049-35329191 | Rare:29 | ||||
| chr19:35510208-35510619 | Rare:99 | ||||
| chr19:35545446-35545734 | Common:4; Rare:95 | ||||
| chr19:35628732-35629113 | Common:4; Rare:116 | ||||
| chr19:35648101-35648402 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745347-35745698 | Rare:107 | ||||
| chr19:35748281-35748646 | Common:3; Rare:103 | ||||
| chr19:35757939-35758204 | Common:2; Rare:79 |