| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49851044-49851212 | Common:1; Rare:68 | ||||
| chr19:49851430-49851830 | Common:1; Rare:125 | ||||
| chr19:49866946-49867334 | Common:3; Rare:143; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr19:49867552-49867703 | Common:3; Rare:41 | ||||
| chr19:49876602-49876888 | Common:1; Rare:94 | ||||
| chr19:49877286-49877451 | Rare:37 | ||||
| chr19:49877831-49878148 | Common:5; Rare:99 | ||||
| chr19:49929394-49929621 | Common:4; Rare:75 | ||||
| chr19:49929921-49930295 | Common:2; Rare:90 | ||||
| chr19:50025906-50026046 | Rare:36 | ||||
| chr19:50203410-50203690 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:50329049-50329277 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:50376286-50376544 | Common:3; Rare:66 | ||||
| chr19:50384010-50384393 | Common:3; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:50476518-50477017 | Rare:271 |