| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45791707-45792552 | Common:12; Rare:601 | ||||
| chr20:45826620-45827107 | Rare:201 | ||||
| chr20:45833568-45833968 | Common:9; Rare:143 | ||||
| chr20:45856730-45857213 | Common:6; Rare:160 | ||||
| chr20:45857298-45857816 | Common:20; Rare:524 | ||||
| chr20:45857814-45858214 | Common:3; Rare:222 | ||||
| chr20:45880944-45881472 | Common:10; Rare:326 | ||||
| chr20:45891097-45891580 | Common:11; Rare:562; Clinvar:23; Clinvar (benign):11 | ||||
| chr20:45910760-45911270 | Common:28; Rare:637 | ||||
| chr20:45911888-45912742 | Common:25; Rare:477 | ||||
| chr20:45934201-45935535 | Common:23; Rare:1661 | ||||
| chr20:45944182-45944582 | Common:1; Rare:78 | ||||
| chr20:45969735-45970428 | Common:4; Rare:132 | ||||
| chr20:45970988-45971782 | Common:2; Rare:223; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:45971721-45972073 | Common:10; Rare:249 |