| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58309426-58309728 | Common:2; Rare:115 | ||||
| chr20:62143301-62143757 | Common:6; Rare:191 | ||||
| chr20:62937893-62938159 | Common:1; Rare:91 | ||||
| chr20:63658250-63658364 | Common:2; Rare:40 | ||||
| chr20:63707290-63707423 | Rare:44 | ||||
| chr20:63707872-63708101 | Rare:66 | ||||
| chr20:63865039-63865351 | Common:2; Rare:111 | ||||
| chr20:64255672-64255771 | Common:2; Rare:48 | ||||
| chr21:25734865-25734983 | Common:2; Rare:55 | ||||
| chr21:25735602-25735932 | Common:4; Rare:86 | ||||
| chr21:28992819-28993039 | Common:1; Rare:103 | ||||
| chr21:29019283-29019403 | Common:5; Rare:51 | ||||
| chr21:29024526-29024719 | Common:2; Rare:82 | ||||
| chr21:29298734-29298935 | Common:1; Rare:86 | ||||
| chr21:31659519-31659837 | Common:2; Rare:138; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 |