| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45076409-45076668 | Rare:76 | ||||
| chr19:45079066-45079380 | Common:1; Rare:83 | ||||
| chr19:45079590-45079663 | Common:1; Rare:17 | ||||
| chr19:45091542-45091859 | Common:2; Rare:83 | ||||
| chr19:45091981-45092090 | Common:1; Rare:24 | ||||
| chr19:45092741-45092958 | Common:2; Rare:64 | ||||
| chr19:45093109-45093294 | Common:3; Rare:61 | ||||
| chr19:45093377-45093517 | Rare:41 | ||||
| chr19:45153702-45154004 | Common:1; Rare:101 | ||||
| chr19:45177918-45178028 | Rare:24 | ||||
| chr19:45178172-45178571 | Common:4; Rare:127 | ||||
| chr19:45178595-45179089 | Common:5; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45179362-45179458 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45179533-45179701 | Common:4; Rare:58; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45251134-45251312 | Common:2; Rare:68 |