| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34955724-34955922 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35172112-35172147 | Rare:14 | ||||
| chr20:35284475-35284588 | Common:2; Rare:39 | ||||
| chr20:35284657-35284840 | Common:1; Rare:62 | ||||
| chr20:35314905-35315222 | Common:2; Rare:47 | ||||
| chr20:35411945-35412074 | Rare:48 | ||||
| chr20:35454809-35455334 | Common:1; Rare:148 | ||||
| chr20:35632319-35632526 | Rare:52 | ||||
| chr20:35699304-35699454 | Rare:50; Clinvar (benign):3 | ||||
| chr20:35713019-35713296 | Common:2; Rare:58 | ||||
| chr20:36236436-36236507 | Rare:14 | ||||
| chr20:36573300-36573682 | Common:2; Rare:154 | ||||
| chr20:36605496-36605826 | Common:2; Rare:121 | ||||
| chr20:36746055-36746297 | Common:2; Rare:87 | ||||
| chr20:37095962-37096030 | Rare:29 |