| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44914305-44914821 | Common:4; Rare:117 | ||||
| chr19:44954575-44954618 | Rare:9 | ||||
| chr19:44954931-44955017 | Common:2; Rare:26 | ||||
| chr19:45038951-45039104 | Rare:54 | ||||
| chr19:45091513-45091815 | Common:2; Rare:82 | ||||
| chr19:45092816-45093150 | Common:2; Rare:98 | ||||
| chr19:45099608-45099746 | Rare:25 | ||||
| chr19:45099891-45100032 | Common:1; Rare:35 | ||||
| chr19:45178727-45178800 | Common:3; Rare:21; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:45370548-45370731 | Common:2; Rare:53 | ||||
| chr19:45406290-45406694 | Common:3; Rare:99 | ||||
| chr19:45423469-45423653 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr19:45423821-45423984 | Common:2; Rare:33 | ||||
| chr19:45506478-45506629 | Common:2; Rare:39 | ||||
| chr19:45506832-45506963 | Common:1; Rare:37 |