| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35003369-35003528 | Rare:40 | ||||
| chr19:35038363-35038454 | Rare:19 | ||||
| chr19:35086011-35086229 | Rare:41 | ||||
| chr19:35124507-35124733 | Common:3; Rare:55 | ||||
| chr19:35155681-35155761 | Common:2; Rare:28 | ||||
| chr19:35205764-35206046 | Common:2; Rare:45 | ||||
| chr19:35206548-35206756 | Common:1; Rare:38 | ||||
| chr19:35210810-35211007 | Rare:30 | ||||
| chr19:35267689-35267759 | Rare:28 | ||||
| chr19:35268007-35268193 | Common:6; Rare:80 | ||||
| chr19:35295972-35295998 | Common:1; Rare:7; Clinvar (benign):1 | ||||
| chr19:35330572-35330840 | Common:1; Rare:59 | ||||
| chr19:35334156-35334601 | Common:6; Rare:69 | ||||
| chr19:35334802-35335221 | Common:7; Rare:73 | ||||
| chr19:35347629-35347916 | Common:1; Rare:53 |