| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17469452-17469652 | Common:1; Rare:46 | ||||
| chr19:17475665-17475915 | Rare:39 | ||||
| chr19:17507770-17508320 | Common:4; Rare:92 | ||||
| chr19:17605794-17606154 | Common:3; Rare:107 | ||||
| chr19:17606278-17606545 | Common:5; Rare:86 | ||||
| chr19:17655025-17655315 | Common:1; Rare:63 | ||||
| chr19:17680207-17680498 | Common:3; Rare:59 | ||||
| chr19:17686746-17687048 | Common:2; Rare:67 | ||||
| chr19:17687295-17687420 | Common:3; Rare:27 | ||||
| chr19:17766766-17766893 | Rare:42 | ||||
| chr19:17779525-17779809 | Common:4; Rare:37 | ||||
| chr19:17830140-17830472 | Common:3; Rare:68; Clinvar:1 | ||||
| chr19:17830571-17831009 | Common:2; Rare:71 | ||||
| chr19:17841509-17841616 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:17855580-17855920 | Rare:82 |