| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:38498387-38498750 | Common:1; Rare:52 | ||||
| chr21:39183381-39183592 | Common:6; Rare:88 | ||||
| chr21:41426108-41426263 | Common:2; Rare:36 | ||||
| chr21:42893050-42893342 | Common:4; Rare:97 | ||||
| chr21:43659468-43659620 | Common:1; Rare:49 | ||||
| chr21:43789375-43789630 | Common:1; Rare:94 | ||||
| chr21:44801739-44801890 | Rare:65 | ||||
| chr21:44872590-44872690 | Rare:24 | ||||
| chr21:44873600-44874050 | Common:8; Rare:181 | ||||
| chr21:45287879-45288093 | Common:5; Rare:82 | ||||
| chr21:46184409-46184736 | Common:4; Rare:31 | ||||
| chr21:46286256-46286396 | Common:4; Rare:52 | ||||
| chr21:46323817-46324153 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr21:46635487-46635723 | Common:5; Rare:80 | ||||
| chr22:17628698-17628914 | Common:1; Rare:80 |