| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63865036-63865379 | Common:2; Rare:124 | ||||
| chr20:63956381-63956705 | Common:1; Rare:123 | ||||
| chr20:63969831-63970034 | Common:2; Rare:68 | ||||
| chr20:64079909-64080112 | Common:2; Rare:84 | ||||
| chr20:64255600-64255771 | Common:3; Rare:91 | ||||
| chr21:25734855-25735557 | Common:5; Rare:232 | ||||
| chr21:25735603-25735933 | Common:4; Rare:87 | ||||
| chr21:26170668-26170881 | Common:3; Rare:72; Clinvar:4; Clinvar (benign):2 | ||||
| chr21:28992819-28993082 | Common:2; Rare:112 | ||||
| chr21:29019297-29019416 | Common:5; Rare:50 | ||||
| chr21:29051461-29051727 | Common:1; Rare:45 | ||||
| chr21:29073528-29073872 | Common:2; Rare:108 | ||||
| chr21:29298746-29298947 | Common:2; Rare:88 | ||||
| chr21:31659515-31659840 | Common:2; Rare:141; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31731951-31732291 | Common:4; Rare:143 |