| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45995008-45995534 | Common:4; Rare:214 | ||||
| chr19:46077039-46077221 | Common:1; Rare:26 | ||||
| chr19:46147368-46147545 | Rare:36 | ||||
| chr19:46147822-46148079 | Rare:43 | ||||
| chr19:46148092-46148262 | Rare:24 | ||||
| chr19:46303341-46303670 | Common:2; Rare:52 | ||||
| chr19:46303740-46303899 | Rare:46 | ||||
| chr19:46303914-46304404 | Common:3; Rare:145 | ||||
| chr19:46346675-46347152 | Common:3; Rare:137 | ||||
| chr19:46347432-46347502 | Rare:16 | ||||
| chr19:46413552-46413749 | Common:1; Rare:64 | ||||
| chr19:46600567-46600699 | Rare:35 | ||||
| chr19:46600836-46601411 | Common:5; Rare:193; Clinvar (benign):1 | ||||
| chr19:46634083-46634242 | Common:2; Rare:48 | ||||
| chr19:46634247-46634492 | Common:1; Rare:36 |