| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580528-49580681 | Rare:49 | ||||
| chr19:49581356-49581412 | Rare:16 | ||||
| chr19:49641826-49642062 | Rare:70 | ||||
| chr19:49665590-49666020 | Common:6; Rare:199; Clinvar (pathogenic):1 | ||||
| chr19:49813249-49813328 | Rare:33 | ||||
| chr19:49851028-49851120 | Rare:41 | ||||
| chr19:49867518-49867650 | Common:2; Rare:41; Clinvar:1 | ||||
| chr19:49877264-49877742 | Common:2; Rare:125 | ||||
| chr19:49877910-49878116 | Common:2; Rare:63 | ||||
| chr19:49929439-49929564 | Common:4; Rare:47 | ||||
| chr19:50025335-50025722 | Common:7; Rare:125 | ||||
| chr19:50476395-50476547 | Rare:74 | ||||
| chr19:50511142-50511330 | Rare:68 | ||||
| chr19:50804592-50804911 | Common:6; Rare:96 | ||||
| chr19:51366283-51366607 | Common:8; Rare:101; Clinvar (benign):2 |