| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:52336143-52336347 | Common:4; Rare:73 | ||||
| chr19:52397725-52397919 | Common:6; Rare:63 | ||||
| chr19:52690455-52690673 | Common:4; Rare:52 | ||||
| chr19:52735013-52735179 | Common:4; Rare:46 | ||||
| chr19:52962861-52963007 | Common:3; Rare:50 | ||||
| chr19:53193321-53193504 | Common:1; Rare:39 | ||||
| chr19:53254793-53255011 | Common:2; Rare:75 | ||||
| chr19:53333573-53333770 | Common:4; Rare:61 | ||||
| chr19:53431759-53432013 | Common:6; Rare:75 | ||||
| chr19:53866057-53866395 | Common:2; Rare:72 | ||||
| chr19:53867682-53867941 | Common:1; Rare:68 | ||||
| chr19:53869279-53869726 | Common:3; Rare:119 | ||||
| chr19:54102616-54102887 | Common:4; Rare:74 | ||||
| chr19:54115271-54115424 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr19:54115613-54115797 | Common:2; Rare:47; Clinvar:5 |