| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48478027-48478317 | Rare:110 | ||||
| chr19:48478335-48478545 | Rare:81 | ||||
| chr19:48812268-48812536 | Common:5; Rare:66 | ||||
| chr19:48962452-48962556 | Common:1; Rare:25 | ||||
| chr19:48969593-48969784 | Rare:56 | ||||
| chr19:49090308-49090514 | Rare:48 | ||||
| chr19:49103527-49103936 | Common:1; Rare:132 | ||||
| chr19:49107671-49107886 | Rare:75 | ||||
| chr19:49491419-49491954 | Common:6; Rare:155 | ||||
| chr19:49635736-49635936 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:49689448-49689607 | Rare:35 | ||||
| chr19:49798662-49798948 | Rare:69 | ||||
| chr19:50205929-50206038 | Common:1; Rare:20 | ||||
| chr19:50491557-50491589 | Rare:5 | ||||
| chr19:50491748-50491965 | Common:2; Rare:68 |