| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19516157-19516331 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19628163-19628318 | Rare:38 | ||||
| chr19:19668658-19668949 | Common:3; Rare:90 | ||||
| chr19:19799498-19799795 | Common:3; Rare:54 | ||||
| chr19:19821637-19821905 | Common:1; Rare:90 | ||||
| chr19:19900778-19901038 | Common:3; Rare:64 | ||||
| chr19:20039207-20039313 | Common:1; Rare:24 | ||||
| chr19:20167173-20167254 | Rare:48 | ||||
| chr19:20661460-20661752 | Common:7; Rare:86 | ||||
| chr19:21396942-21397198 | Rare:69 | ||||
| chr19:22532477-22532680 | Common:1; Rare:48 | ||||
| chr19:22634129-22634358 | Common:7; Rare:67 | ||||
| chr19:23687107-23687324 | Common:4; Rare:55 | ||||
| chr19:29212980-29213219 | Common:3; Rare:68 | ||||
| chr19:29606186-29606323 | Rare:46 |