| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:52527438-52527696 | Common:3; Rare:87 | ||||
| chr19:52638332-52638610 | Common:4; Rare:66 | ||||
| chr19:52735021-52735167 | Common:3; Rare:39 | ||||
| chr19:52897605-52897827 | Rare:63 | ||||
| chr19:52962861-52963056 | Common:3; Rare:61 | ||||
| chr19:53159022-53159189 | Common:3; Rare:72 | ||||
| chr19:53193321-53193520 | Common:2; Rare:42 | ||||
| chr19:53254785-53255019 | Common:2; Rare:79 | ||||
| chr19:53333560-53333768 | Common:3; Rare:66 | ||||
| chr19:53395019-53395165 | Common:4; Rare:47 | ||||
| chr19:53538000-53538191 | Common:4; Rare:77 | ||||
| chr19:53866059-53866399 | Common:2; Rare:73 | ||||
| chr19:53867572-53867943 | Common:1; Rare:92 | ||||
| chr19:54115289-54115431 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr19:54115638-54115787 | Common:1; Rare:31; Clinvar:4 |