| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53866311-53866531 | Common:4; Rare:55 | ||||
| chr19:53867444-53867469 | Rare:4 | ||||
| chr19:53867543-53868008 | Common:3; Rare:106 | ||||
| chr19:53868610-53869056 | Common:2; Rare:87 | ||||
| chr19:53869072-53869826 | Common:6; Rare:186 | ||||
| chr19:53879330-53879720 | Common:4; Rare:91 | ||||
| chr19:53881838-53881897 | Common:1; Rare:4 | ||||
| chr19:53881977-53882207 | Common:1; Rare:51 | ||||
| chr19:53882247-53882329 | Rare:27; Clinvar:2 | ||||
| chr19:54102587-54102901 | Common:5; Rare:86 | ||||
| chr19:54115276-54115429 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr19:54115603-54115824 | Common:3; Rare:60; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:54136942-54137486 | Common:5; Rare:145 | ||||
| chr19:54137707-54137833 | Common:1; Rare:48 | ||||
| chr19:54138269-54138364 | Rare:19 |