| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:52821630-52821714 | Rare:18 | ||||
| chr19:52897605-52897730 | Rare:38 | ||||
| chr19:52962817-52963082 | Common:4; Rare:84 | ||||
| chr19:53132869-53132934 | Common:2; Rare:21 | ||||
| chr19:53254793-53255054 | Common:4; Rare:93 | ||||
| chr19:53333560-53333770 | Common:4; Rare:67 | ||||
| chr19:53431717-53432031 | Common:6; Rare:93 | ||||
| chr19:53520751-53521032 | Common:12; Rare:66 | ||||
| chr19:53538095-53538363 | Common:5; Rare:79 | ||||
| chr19:53554231-53554665 | Common:3; Rare:130 | ||||
| chr19:53866222-53866399 | Common:2; Rare:36 | ||||
| chr19:53867621-53867943 | Common:1; Rare:82 | ||||
| chr19:53869287-53869786 | Common:3; Rare:135 | ||||
| chr19:54102674-54102898 | Common:3; Rare:60 | ||||
| chr19:54115265-54115425 | Common:1; Rare:38; Clinvar (benign):1 |