| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63865066-63865362 | Common:2; Rare:113 | ||||
| chr20:63956373-63956656 | Common:1; Rare:107 | ||||
| chr20:63980951-63981243 | Common:4; Rare:98; Clinvar:7; Clinvar (benign):4 | ||||
| chr21:14383111-14383486 | Common:2; Rare:105 | ||||
| chr21:17512741-17513163 | Common:2; Rare:129 | ||||
| chr21:17819327-17819435 | Common:1; Rare:40 | ||||
| chr21:25607473-25607612 | Rare:66 | ||||
| chr21:25639144-25639405 | Common:3; Rare:53 | ||||
| chr21:25734853-25735440 | Common:3; Rare:207 | ||||
| chr21:25735644-25735902 | Common:4; Rare:71 | ||||
| chr21:26170645-26170900 | Common:3; Rare:84; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:28885341-28885425 | Common:2; Rare:65 | ||||
| chr21:28992788-28993110 | Common:2; Rare:135 | ||||
| chr21:29019321-29019400 | Common:5; Rare:31 | ||||
| chr21:29024530-29024726 | Common:2; Rare:86 |