| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:14527655-14527756 | Rare:22 | ||||
| chr19:14556744-14556869 | Rare:34 | ||||
| chr19:14574271-14574501 | Common:2; Rare:36 | ||||
| chr19:14632445-14632563 | Rare:28 | ||||
| chr19:14731291-14731461 | Common:2; Rare:37 | ||||
| chr19:15249030-15249168 | Rare:32 | ||||
| chr19:15377994-15378268 | Common:1; Rare:69 | ||||
| chr19:15551582-15551782 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:15555832-15556096 | Common:2; Rare:66 | ||||
| chr19:15556506-15556609 | Rare:21 | ||||
| chr19:15563428-15563655 | Rare:37 | ||||
| chr19:15584700-15584980 | Common:3; Rare:59 | ||||
| chr19:15828330-15828590 | Common:2; Rare:44 | ||||
| chr19:15828819-15828954 | Common:2; Rare:23 | ||||
| chr19:15836798-15837272 | Common:4; Rare:131 |