| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45001838-45001937 | Common:1; Rare:34 | ||||
| chr19:45038932-45039147 | Rare:77 | ||||
| chr19:45039311-45039384 | Common:2; Rare:19 | ||||
| chr19:45039418-45039461 | Rare:14 | ||||
| chr19:45076337-45076617 | Common:1; Rare:95 | ||||
| chr19:45079069-45079386 | Common:1; Rare:85 | ||||
| chr19:45079651-45079822 | Common:1; Rare:51 | ||||
| chr19:45091570-45091840 | Common:2; Rare:69 | ||||
| chr19:45092021-45092301 | Common:9; Rare:80 | ||||
| chr19:45092740-45093249 | Common:4; Rare:152 | ||||
| chr19:45178147-45178397 | Common:2; Rare:91 | ||||
| chr19:45178444-45178888 | Common:7; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45178946-45179087 | Rare:31 | ||||
| chr19:45179357-45179451 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45179500-45179583 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 |