| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:16194265-16194607 | Common:2; Rare:94 | ||||
| chr21:16419472-16419752 | Common:2; Rare:57 | ||||
| chr21:16420266-16420585 | Common:1; Rare:57 | ||||
| chr21:16537160-16537287 | Common:1; Rare:22 | ||||
| chr21:26964482-26964743 | Common:1; Rare:51 | ||||
| chr21:26967086-26967294 | Rare:47 | ||||
| chr21:28048281-28048457 | Common:2; Rare:26 | ||||
| chr21:29002719-29002861 | Common:2; Rare:52 | ||||
| chr21:33976193-33976529 | Common:8; Rare:74 | ||||
| chr21:37221292-37221444 | Common:2; Rare:69 | ||||
| chr21:37555922-37556197 | Common:1; Rare:52 | ||||
| chr21:37751393-37751565 | Common:1; Rare:37 | ||||
| chr21:39788512-39788716 | Common:2; Rare:49 | ||||
| chr21:43332102-43332288 | Rare:41 | ||||
| chr21:45992187-45992397 | Common:1; Rare:72; Clinvar:9; Clinvar (benign):3 |