| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43666804-43667317 | Common:28; Rare:879 | ||||
| chr20:43667428-43667828 | Rare:87 | ||||
| chr20:44038775-44039175 | Rare:106 | ||||
| chr20:44210318-44210718 | Common:2; Rare:150 | ||||
| chr20:44210691-44211167 | Common:34; Rare:957 | ||||
| chr20:44310269-44311175 | Common:5; Rare:284 | ||||
| chr20:44311110-44311444 | Common:2; Rare:221 | ||||
| chr20:44475700-44476100 | Common:5; Rare:511 | ||||
| chr20:44521343-44521855 | Common:4; Rare:257 | ||||
| chr20:44521928-44522328 | Common:12; Rare:401 | ||||
| chr20:44522605-44523005 | Rare:59 | ||||
| chr20:44531550-44532120 | Common:9; Rare:478 | ||||
| chr20:44582260-44582719 | Rare:151 | ||||
| chr20:44614617-44615017 | Common:5; Rare:144 | ||||
| chr20:44651560-44651910 | Common:5; Rare:237; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |