| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39435848-39436212 | Common:18; Rare:276 | ||||
| chr19:39445230-39445740 | Common:10; Rare:282 | ||||
| chr19:39480606-39480955 | Common:6; Rare:282; Clinvar (pathogenic):2 | ||||
| chr19:39840080-39840530 | Common:2; Rare:239 | ||||
| chr19:39840550-39840960 | Common:2; Rare:235 | ||||
| chr19:39846308-39846517 | Common:2; Rare:184 | ||||
| chr19:39970747-39971218 | Common:11; Rare:205 | ||||
| chr19:39996787-39997156 | Common:10; Rare:144 | ||||
| chr19:40056154-40056292 | Rare:35 | ||||
| chr19:40090858-40091015 | Common:2; Rare:76 | ||||
| chr19:40191340-40191516 | Common:4; Rare:75 | ||||
| chr19:40285235-40285727 | Common:10; Rare:318 | ||||
| chr19:40348319-40348753 | Common:8; Rare:274 | ||||
| chr19:40365252-40366042 | Common:8; Rare:375 | ||||
| chr19:40425783-40426160 | Common:4; Rare:173 |