| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5622711-5623203 | Common:5; Rare:197 | ||||
| chr19:5680456-5680614 | Rare:48 | ||||
| chr19:5680943-5681169 | Rare:75 | ||||
| chr19:5791150-5791343 | Common:5; Rare:60 | ||||
| chr19:5903695-5903890 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:5978069-5978395 | Common:3; Rare:123 | ||||
| chr19:6416839-6417019 | Common:1; Rare:66 | ||||
| chr19:6739519-6739754 | Common:5; Rare:67 | ||||
| chr19:6740627-6740933 | Common:1; Rare:69 | ||||
| chr19:7395036-7395209 | Common:4; Rare:55 | ||||
| chr19:7488988-7489103 | Rare:52 | ||||
| chr19:7534024-7534187 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chr19:7535574-7535769 | Common:3; Rare:69 | ||||
| chr19:7629528-7629844 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637003-7637143 | Common:2; Rare:48; Clinvar (benign):1 |