| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39410548-39410744 | Common:1; Rare:41 | ||||
| chr19:39411502-39411710 | Common:2; Rare:41 | ||||
| chr19:40810801-40810903 | Common:2; Rare:22 | ||||
| chr19:41238602-41238670 | Rare:16 | ||||
| chr19:41352935-41352982 | Common:1; Rare:15; Clinvar (benign):1 | ||||
| chr19:43329052-43329222 | Common:2; Rare:24 | ||||
| chr19:45509338-45509518 | Common:1; Rare:52 | ||||
| chr19:46860914-46861126 | Common:1; Rare:75 | ||||
| chr19:48873045-48873177 | Common:2; Rare:17 | ||||
| chr19:48966275-48966729 | Rare:153; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr19:49103548-49103786 | Common:1; Rare:75 | ||||
| chr19:49491464-49491785 | Common:2; Rare:96 | ||||
| chr19:58551470-58551705 | Common:1; Rare:85 | ||||
| chr2:9535834-9536009 | Rare:37 | ||||
| chr2:20033017-20033488 | Common:1; Rare:96 |