| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45295372-45295595 | Common:1; Rare:53 | ||||
| chr21:45512015-45512251 | Common:2; Rare:86; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr21:45519321-45519532 | Common:3; Rare:35 | ||||
| chr21:46251713-46251842 | Common:3; Rare:31 | ||||
| chr21:46649873-46650079 | Common:1; Rare:34 | ||||
| chr21:46653570-46653926 | Rare:74 | ||||
| chr21:46659942-46660021 | Rare:18 | ||||
| chr22:12602016-12602336 | Rare:19 | ||||
| chr22:20702614-20703000 | Common:3; Rare:95 | ||||
| chr22:20918211-20918242 | Rare:7 | ||||
| chr22:21014151-21014454 | Rare:80 | ||||
| chr22:22297948-22298199 | Common:12; Rare:107 | ||||
| chr22:24019416-24019602 | Common:1; Rare:37 | ||||
| chr22:24384162-24384218 | Rare:10 | ||||
| chr22:24402636-24402693 | Common:1; Rare:10 |