| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45038860-45039120 | Rare:85 | ||||
| chr19:45079147-45079270 | Rare:32 | ||||
| chr19:45090953-45091358 | Common:4; Rare:119 | ||||
| chr19:45091564-45091843 | Common:2; Rare:71 | ||||
| chr19:45092797-45093221 | Common:4; Rare:124 | ||||
| chr19:45178178-45178405 | Common:3; Rare:82 | ||||
| chr19:45178626-45178809 | Common:4; Rare:43; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:45250900-45251360 | Common:2; Rare:135 | ||||
| chr19:45370522-45370854 | Common:2; Rare:103; Clinvar:1 | ||||
| chr19:45406044-45406156 | Common:1; Rare:31 | ||||
| chr19:45406326-45406694 | Common:3; Rare:90 | ||||
| chr19:45423481-45423679 | Common:2; Rare:39; Clinvar (benign):1 | ||||
| chr19:45423848-45424110 | Common:3; Rare:62 | ||||
| chr19:45450720-45451040 | Common:4; Rare:61 | ||||
| chr19:45469623-45470023 | Common:5; Rare:133 |