| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35155148-35155218 | Rare:15 | ||||
| chr19:35155306-35155603 | Rare:76 | ||||
| chr19:35248878-35249144 | Common:2; Rare:119 | ||||
| chr19:35266413-35266960 | Common:3; Rare:192 | ||||
| chr19:35268421-35268546 | Rare:17 | ||||
| chr19:35545460-35545726 | Common:4; Rare:86 | ||||
| chr19:35563372-35563708 | Common:2; Rare:125 | ||||
| chr19:35628711-35629187 | Common:5; Rare:140 | ||||
| chr19:35648113-35648402 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35717497-35717608 | Common:1; Rare:31 | ||||
| chr19:35745347-35745873 | Rare:131 | ||||
| chr19:35748256-35748635 | Common:3; Rare:107 | ||||
| chr19:35757004-35757173 | Rare:32 | ||||
| chr19:35757906-35758204 | Common:2; Rare:87 | ||||
| chr19:35899705-35899865 | Common:1; Rare:47 |