| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25339695-25339816 | Rare:24 | ||||
| chr20:25390701-25391088 | Common:8; Rare:278; Clinvar:8; Clinvar (benign):5 | ||||
| chr20:25407503-25407785 | Common:5; Rare:175; Clinvar (pathogenic):2 | ||||
| chr20:25585167-25585303 | Common:1; Rare:41 | ||||
| chr20:25585420-25585757 | Common:7; Rare:155 | ||||
| chr20:25623630-25624197 | Common:2; Rare:345 | ||||
| chr20:25624250-25624650 | Common:5; Rare:142 | ||||
| chr20:25696759-25697098 | Common:6; Rare:176 | ||||
| chr20:31547236-31547472 | Rare:109 | ||||
| chr20:31605090-31605412 | Common:18; Rare:324 | ||||
| chr20:31722441-31722982 | Common:2; Rare:221 | ||||
| chr20:31723185-31723775 | Common:5; Rare:303 | ||||
| chr20:31739070-31739551 | Common:4; Rare:178 | ||||
| chr20:31870210-31870710 | Common:4; Rare:201 | ||||
| chr20:32109418-32109589 | Common:1; Rare:34 |