| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:56392182-56392436 | Common:1; Rare:73 | ||||
| chr20:56392457-56392683 | Common:5; Rare:49 | ||||
| chr20:56468318-56468710 | Rare:126 | ||||
| chr20:58388984-58389275 | Common:3; Rare:131; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58515390-58515521 | Common:2; Rare:23 | ||||
| chr20:58651133-58651289 | Common:2; Rare:34; Clinvar (benign):1 | ||||
| chr20:58909684-58910081 | Common:1; Rare:68; Clinvar (pathogenic):2 | ||||
| chr20:59032229-59032560 | Common:3; Rare:142; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59940303-59940494 | Rare:76 | ||||
| chr20:62143288-62143729 | Common:6; Rare:182 | ||||
| chr20:62182953-62183050 | Rare:24 | ||||
| chr20:62386946-62387136 | Common:3; Rare:84 | ||||
| chr20:62937849-62938193 | Common:2; Rare:127 | ||||
| chr20:62952591-62952776 | Common:2; Rare:49 | ||||
| chr20:63272721-63272883 | Common:1; Rare:57 |