| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:25735494-25735906 | Common:4; Rare:104 | ||||
| chr21:26170562-26170928 | Common:6; Rare:119; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26171123-26171183 | Rare:15 | ||||
| chr21:26845407-26845641 | Common:2; Rare:64 | ||||
| chr21:28885337-28885431 | Common:2; Rare:71 | ||||
| chr21:28992792-28993064 | Common:1; Rare:118 | ||||
| chr21:29019297-29019443 | Common:5; Rare:62 | ||||
| chr21:29024526-29024745 | Common:2; Rare:98 | ||||
| chr21:29024876-29025025 | Rare:29 | ||||
| chr21:29073568-29073870 | Common:2; Rare:93 | ||||
| chr21:29298582-29298942 | Common:2; Rare:136 | ||||
| chr21:29939381-29939409 | Rare:9 | ||||
| chr21:29939622-29939801 | Common:1; Rare:40 | ||||
| chr21:29939803-29939875 | Common:2; Rare:15 | ||||
| chr21:29939953-29940164 | Common:2; Rare:64 |