| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77862648-77862863 | Common:3; Rare:75 | ||||
| chr4:80072707-80072832 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr4:80073037-80073160 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:81471819-81472075 | Common:1; Rare:84 | ||||
| chr4:82373887-82374343 | Common:3; Rare:145 | ||||
| chr4:82429247-82429594 | Common:1; Rare:191; Clinvar:10; Clinvar (benign):6 | ||||
| chr4:82890985-82891317 | Common:1; Rare:122 | ||||
| chr4:82900439-82900732 | Common:1; Rare:85 | ||||
| chr4:83034888-83035230 | Common:1; Rare:85 | ||||
| chr4:83455779-83456083 | Common:2; Rare:115 | ||||
| chr4:83485084-83485287 | Common:3; Rare:85 | ||||
| chr4:84966555-84966704 | Rare:39 | ||||
| chr4:86594055-86594362 | Rare:99 | ||||
| chr4:86934892-86935114 | Common:2; Rare:101 | ||||
| chr4:86936167-86936332 | Rare:39 |