| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51366271-51366537 | Common:5; Rare:79; Clinvar (benign):2 | ||||
| chr19:51751852-51751987 | Common:2; Rare:28 | ||||
| chr19:52008166-52008290 | Rare:38 | ||||
| chr19:52028302-52028462 | Common:3; Rare:42 | ||||
| chr19:52028579-52028725 | Rare:27 | ||||
| chr19:52048632-52048687 | Rare:9 | ||||
| chr19:52397690-52397907 | Common:5; Rare:69 | ||||
| chr19:52962817-52963082 | Common:4; Rare:84 | ||||
| chr19:53254793-53255014 | Common:2; Rare:75 | ||||
| chr19:53869393-53869697 | Common:1; Rare:82 | ||||
| chr19:54102674-54102904 | Common:4; Rare:63 | ||||
| chr19:54115280-54115455 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr19:54115596-54115795 | Common:2; Rare:51; Clinvar:6 | ||||
| chr19:54159668-54160079 | Rare:138 | ||||
| chr19:54160972-54161083 | Common:2; Rare:29 |