| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33811493-33811631 | Rare:29 | ||||
| chr20:33993079-33993308 | Rare:59 | ||||
| chr20:34112216-34112475 | Common:1; Rare:81 | ||||
| chr20:34302978-34303314 | Common:1; Rare:116; Clinvar (benign):2 | ||||
| chr20:34704187-34704354 | Common:1; Rare:52 | ||||
| chr20:34955733-34956095 | Common:1; Rare:116; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:35278052-35278327 | Common:6; Rare:95 | ||||
| chr20:35284745-35284863 | Common:1; Rare:41 | ||||
| chr20:35542329-35542524 | Rare:67 | ||||
| chr20:35664881-35665042 | Common:1; Rare:41 | ||||
| chr20:35742334-35742673 | Common:6; Rare:114 | ||||
| chr20:35771784-35772075 | Common:2; Rare:89 | ||||
| chr20:36773749-36774004 | Common:2; Rare:80 | ||||
| chr20:36951611-36951714 | Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:36951752-36951917 | Rare:42; Clinvar (benign):1 |