| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7489000-7489175 | Common:2; Rare:78 | ||||
| chr19:7515923-7516228 | Rare:74 | ||||
| chr19:7534103-7534188 | Common:3; Rare:22; Clinvar (benign):1 | ||||
| chr19:7535574-7535747 | Common:3; Rare:57 | ||||
| chr19:7629500-7629844 | Common:7; Rare:128; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7943627-7944017 | Rare:114 | ||||
| chr19:8005514-8005822 | Common:1; Rare:109 | ||||
| chr19:8308288-8308647 | Common:3; Rare:116; Clinvar (benign):1 | ||||
| chr19:8321324-8321703 | Common:2; Rare:153 | ||||
| chr19:8390056-8390419 | Common:1; Rare:101 | ||||
| chr19:8444773-8445118 | Common:4; Rare:152; Clinvar (benign):1 | ||||
| chr19:8514149-8514227 | Common:1; Rare:20 | ||||
| chr19:8832213-8832358 | Common:1; Rare:54 | ||||
| chr19:9140299-9140444 | Common:2; Rare:39 | ||||
| chr19:9324043-9324403 | Common:7; Rare:155 |