| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46788559-46788861 | Common:2; Rare:66 | ||||
| chr19:47112165-47112333 | Rare:52 | ||||
| chr19:47113097-47113430 | Common:2; Rare:89 | ||||
| chr19:47256472-47256577 | Rare:39 | ||||
| chr19:47349088-47349352 | Rare:73 | ||||
| chr19:47484190-47484307 | Common:1; Rare:36 | ||||
| chr19:47745419-47745572 | Rare:73 | ||||
| chr19:47778385-47778781 | Common:3; Rare:141 | ||||
| chr19:48170246-48170699 | Common:2; Rare:125 | ||||
| chr19:48619139-48619534 | Common:1; Rare:131 | ||||
| chr19:48695849-48696021 | Common:1; Rare:37 | ||||
| chr19:48810997-48811124 | Rare:44 | ||||
| chr19:48993204-48993909 | Common:9; Rare:248; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49064807-49065103 | Rare:75 | ||||
| chr19:49085088-49085515 | Common:3; Rare:170 |