| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42514398-42514556 | Rare:35 | ||||
| chr21:42653467-42653813 | Common:5; Rare:54 | ||||
| chr21:42879023-42879134 | Common:1; Rare:33 | ||||
| chr21:42879439-42879669 | Common:3; Rare:97 | ||||
| chr21:42893063-42893378 | Common:4; Rare:112 | ||||
| chr21:42974242-42974621 | Common:1; Rare:146 | ||||
| chr21:43659435-43659585 | Common:1; Rare:51 | ||||
| chr21:43733863-43734092 | Common:2; Rare:65 | ||||
| chr21:43776204-43776471 | Common:4; Rare:92; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789371-43789630 | Common:1; Rare:95 | ||||
| chr21:44299967-44300123 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr21:44333307-44333343 | Rare:7 | ||||
| chr21:44339203-44339467 | Common:2; Rare:82 | ||||
| chr21:44353542-44353661 | Common:1; Rare:22 | ||||
| chr21:44455277-44455584 | Common:4; Rare:73 |