| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39480591-39480931 | Common:3; Rare:163; Clinvar (pathogenic):1 | ||||
| chr19:39846296-39846499 | Common:1; Rare:97 | ||||
| chr19:39970948-39971203 | Common:3; Rare:70 | ||||
| chr19:40056157-40056272 | Rare:16 | ||||
| chr19:40090864-40090951 | Common:1; Rare:29 | ||||
| chr19:40285243-40285557 | Common:1; Rare:114 | ||||
| chr19:40348388-40348746 | Common:4; Rare:119 | ||||
| chr19:40425982-40426147 | Common:1; Rare:48 | ||||
| chr19:40444287-40444517 | Common:3; Rare:71 | ||||
| chr19:40715068-40715148 | Rare:27 | ||||
| chr19:40716118-40716263 | Common:2; Rare:21 | ||||
| chr19:40716861-40717094 | Common:1; Rare:78 | ||||
| chr19:40751033-40751311 | Common:3; Rare:87 | ||||
| chr19:40778007-40778280 | Common:1; Rare:87 | ||||
| chr19:41219115-41219403 | Common:1; Rare:75 |