| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11089300-11089526 | Rare:41; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr19:11155768-11156061 | Common:3; Rare:68 | ||||
| chr19:11197504-11197625 | Common:1; Rare:32 | ||||
| chr19:11197814-11197974 | Rare:51 | ||||
| chr19:11529120-11529294 | Rare:36 | ||||
| chr19:11559189-11559387 | Common:1; Rare:63 | ||||
| chr19:11738889-11739252 | Common:4; Rare:97 | ||||
| chr19:11924956-11925138 | Common:6; Rare:49 | ||||
| chr19:12140335-12140566 | Rare:65 | ||||
| chr19:12333709-12333814 | Rare:22 | ||||
| chr19:12365612-12365784 | Common:3; Rare:47 | ||||
| chr19:12484744-12484932 | Common:1; Rare:45 | ||||
| chr19:12551400-12551734 | Common:2; Rare:91 | ||||
| chr19:12610694-12610989 | Rare:96 | ||||
| chr19:12666704-12666854 | Rare:58; Clinvar:2 |