| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25407542-25407783 | Common:2; Rare:82; Clinvar (pathogenic):1 | ||||
| chr20:25623944-25624194 | Common:1; Rare:93 | ||||
| chr20:25624407-25624547 | Rare:46 | ||||
| chr20:25696762-25697091 | Common:3; Rare:92 | ||||
| chr20:31547260-31547447 | Rare:50 | ||||
| chr20:31605086-31605488 | Common:10; Rare:212 | ||||
| chr20:31605680-31605813 | Common:1; Rare:70 | ||||
| chr20:31722826-31722956 | Rare:33 | ||||
| chr20:31723519-31723713 | Common:1; Rare:53 | ||||
| chr20:31739078-31739375 | Common:2; Rare:78 | ||||
| chr20:31739456-31739574 | Common:1; Rare:10 | ||||
| chr20:32109402-32109642 | Common:1; Rare:48 | ||||
| chr20:32109685-32109780 | Rare:50 | ||||
| chr20:32207670-32207958 | Common:3; Rare:110 | ||||
| chr20:32358477-32358774 | Common:2; Rare:93; Clinvar:10; Clinvar (benign):2 |