| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:55116368-55116518 | Common:1; Rare:40 | ||||
| chr19:55118490-55118950 | Rare:87 | ||||
| chr19:55151966-55152366 | Common:4; Rare:116 | ||||
| chr19:55159001-55159376 | Common:1; Rare:118; Clinvar:11; Clinvar (benign):1 | ||||
| chr19:55173659-55173766 | Rare:18 | ||||
| chr19:55189376-55189622 | Common:3; Rare:62 | ||||
| chr19:55210288-55210416 | Rare:19 | ||||
| chr19:55212460-55212730 | Rare:47 | ||||
| chr19:55216473-55216722 | Common:2; Rare:40 | ||||
| chr19:55216990-55217149 | Rare:39 | ||||
| chr19:55338791-55338897 | Common:1; Rare:14 | ||||
| chr19:55383658-55383981 | Common:1; Rare:76 | ||||
| chr19:55472527-55472736 | Common:3; Rare:44 | ||||
| chr19:55473304-55473522 | Rare:35 | ||||
| chr19:55473621-55474021 | Common:4; Rare:130 |