| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:19211762-19212310 | Common:4; Rare:353 | ||||
| chr20:19212329-19213015 | Common:12; Rare:427 | ||||
| chr20:19213005-19213405 | Common:3; Rare:93 | ||||
| chr20:20017133-20017450 | Rare:189 | ||||
| chr20:20052288-20052707 | Common:8; Rare:189 | ||||
| chr20:20712410-20713130 | Common:9; Rare:506 | ||||
| chr20:21125745-21126162 | Common:6; Rare:227 | ||||
| chr20:21303110-21303456 | Rare:260 | ||||
| chr20:21303640-21304030 | Rare:213 | ||||
| chr20:21513960-21514327 | Rare:77 | ||||
| chr20:22584420-22585190 | Common:5; Rare:238 | ||||
| chr20:23049621-23050039 | Common:9; Rare:326; Clinvar (pathogenic):1 | ||||
| chr20:23350355-23350906 | Common:14; Rare:431 | ||||
| chr20:23361607-23362311 | Common:18; Rare:564 | ||||
| chr20:23421310-23421685 | Common:14; Rare:354 |