| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45079400-45079427 | Rare:5 | ||||
| chr19:45079626-45079876 | Common:2; Rare:69 | ||||
| chr19:45091603-45092301 | Common:12; Rare:187 | ||||
| chr19:45092749-45093240 | Common:4; Rare:145 | ||||
| chr19:45178168-45178401 | Common:2; Rare:83 | ||||
| chr19:45178712-45179264 | Common:4; Rare:133; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45179320-45179426 | Rare:49; Clinvar:1 | ||||
| chr19:45179479-45179576 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:45251117-45251317 | Common:2; Rare:73 | ||||
| chr19:45370526-45370896 | Common:3; Rare:106; Clinvar:1 | ||||
| chr19:45405045-45405279 | Common:1; Rare:45 | ||||
| chr19:45405487-45405571 | Common:2; Rare:13 | ||||
| chr19:45406006-45406160 | Common:1; Rare:35 | ||||
| chr19:45406334-45406710 | Common:3; Rare:94 | ||||
| chr19:45419567-45419746 | Common:1; Rare:34 |