| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033482-19033610 | Common:2; Rare:44 | ||||
| chr19:19516176-19516235 | Rare:27 | ||||
| chr19:32971922-32972262 | Common:4; Rare:96 | ||||
| chr19:33373557-33373812 | Common:2; Rare:85 | ||||
| chr19:33521765-33521963 | Common:1; Rare:59; Clinvar:3 | ||||
| chr19:35545491-35545689 | Common:4; Rare:65 | ||||
| chr19:35745397-35745692 | Rare:88 | ||||
| chr19:36014192-36014551 | Common:2; Rare:97 | ||||
| chr19:36215065-36215176 | Rare:36 | ||||
| chr19:36528248-36528284 | Common:1; Rare:9 | ||||
| chr19:36687419-36687620 | Common:2; Rare:60 | ||||
| chr19:38618975-38619246 | Common:2; Rare:75 | ||||
| chr19:38899621-38900023 | Rare:111 | ||||
| chr19:38930742-38930992 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39391033-39391418 | Common:1; Rare:157 |