| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53159023-53159189 | Common:3; Rare:72 | ||||
| chr19:53193333-53193504 | Common:1; Rare:35 | ||||
| chr19:53254778-53255049 | Common:4; Rare:95 | ||||
| chr19:53333599-53333790 | Common:3; Rare:64 | ||||
| chr19:53365537-53365752 | Common:6; Rare:59 | ||||
| chr19:53395017-53395165 | Common:4; Rare:47 | ||||
| chr19:53431924-53432013 | Common:2; Rare:27 | ||||
| chr19:53520788-53521046 | Common:8; Rare:59 | ||||
| chr19:53538091-53538185 | Common:1; Rare:41 | ||||
| chr19:53554286-53554600 | Common:2; Rare:96 | ||||
| chr19:53866082-53866399 | Common:2; Rare:70 | ||||
| chr19:53867679-53867930 | Common:1; Rare:68 | ||||
| chr19:53909198-53909478 | Common:1; Rare:79 | ||||
| chr19:54102674-54102904 | Common:4; Rare:63 | ||||
| chr19:54115289-54115431 | Common:1; Rare:33; Clinvar (benign):1 |