| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45076333-45076533 | Common:2; Rare:128 | ||||
| chr19:45076434-45076641 | Rare:61 | ||||
| chr19:45079081-45079388 | Common:3; Rare:191 | ||||
| chr19:45091561-45091862 | Common:5; Rare:198 | ||||
| chr19:45092175-45092299 | Common:9; Rare:44 | ||||
| chr19:45092733-45093428 | Common:17; Rare:503 | ||||
| chr19:45178134-45178565 | Common:11; Rare:368 | ||||
| chr19:45178606-45179097 | Common:14; Rare:241; Clinvar:3; Clinvar (benign):12 | ||||
| chr19:45251165-45251332 | Common:2; Rare:134 | ||||
| chr19:45340601-45340829 | Common:6; Rare:193 | ||||
| chr19:45370525-45370894 | Common:7; Rare:273; Clinvar:1 | ||||
| chr19:45404955-45405297 | Common:1; Rare:147 | ||||
| chr19:45405840-45406240 | Common:6; Rare:172 | ||||
| chr19:45406274-45406729 | Common:9; Rare:284 | ||||
| chr19:45423275-45424131 | Common:16; Rare:397; Clinvar (benign):4 |