| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35129980-35130198 | Rare:34 | ||||
| chr19:35262465-35262569 | Rare:34 | ||||
| chr19:35716943-35717123 | Common:2; Rare:33 | ||||
| chr19:36142653-36142966 | Rare:85 | ||||
| chr19:38078273-38078454 | Rare:31 | ||||
| chr19:38649784-38650118 | Common:1; Rare:59 | ||||
| chr19:38696694-38696720 | |||||
| chr19:38700420-38700714 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr19:38801816-38802414 | Common:1; Rare:177 | ||||
| chr19:38819897-38820194 | Common:1; Rare:56 | ||||
| chr19:38822535-38822880 | Common:1; Rare:75 | ||||
| chr19:39409655-39409689 | Rare:7 | ||||
| chr19:39410681-39410877 | Common:3; Rare:32 | ||||
| chr19:39411221-39411403 | Common:1; Rare:42 | ||||
| chr19:39885673-39886013 | Common:1; Rare:93 |