| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45423509-45423659 | Common:2; Rare:31; Clinvar (benign):1 | ||||
| chr19:45423872-45423951 | Common:2; Rare:20 | ||||
| chr19:45469189-45469476 | Common:1; Rare:93 | ||||
| chr19:45506527-45506629 | Common:1; Rare:34 | ||||
| chr19:45507353-45507529 | Rare:55 | ||||
| chr19:45584772-45584985 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45668126-45668240 | Common:1; Rare:24 | ||||
| chr19:45692533-45692742 | Common:1; Rare:57 | ||||
| chr19:45730869-45731084 | Common:1; Rare:50 | ||||
| chr19:45769351-45769622 | Common:1; Rare:126 | ||||
| chr19:45862639-45862829 | Common:1; Rare:55 | ||||
| chr19:45902611-45902935 | Common:3; Rare:95 | ||||
| chr19:46346927-46347142 | Common:3; Rare:69 | ||||
| chr19:46601202-46601416 | Common:3; Rare:64; Clinvar (benign):1 | ||||
| chr19:46717075-46717258 | Common:2; Rare:64 |