| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4472023-4472261 | Common:2; Rare:70 | ||||
| chr19:4498016-4498328 | Common:5; Rare:105 | ||||
| chr19:4639214-4639579 | Common:1; Rare:125 | ||||
| chr19:4831684-4832044 | Common:3; Rare:72 | ||||
| chr19:5293209-5293447 | Common:1; Rare:103 | ||||
| chr19:5622725-5623302 | Common:6; Rare:227 | ||||
| chr19:5641589-5641907 | Rare:92 | ||||
| chr19:5680876-5681173 | Rare:89 | ||||
| chr19:5978066-5978418 | Common:3; Rare:136 | ||||
| chr19:6372519-6372828 | Common:5; Rare:106 | ||||
| chr19:7395047-7395208 | Common:3; Rare:52 | ||||
| chr19:7533901-7534187 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr19:7535569-7535787 | Common:3; Rare:79 | ||||
| chr19:7629529-7629898 | Common:5; Rare:129; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7920176-7920382 | Rare:76 |