| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42879532-42879680 | Common:3; Rare:44 | ||||
| chr21:42893050-42893354 | Common:4; Rare:104 | ||||
| chr21:43659461-43659585 | Common:1; Rare:41 | ||||
| chr21:43733566-43733767 | Rare:45 | ||||
| chr21:43776239-43776677 | Common:5; Rare:154; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr21:43789365-43789624 | Common:1; Rare:94 | ||||
| chr21:44299992-44300105 | Rare:47; Clinvar (benign):1 | ||||
| chr21:44801707-44801876 | Rare:67 | ||||
| chr21:44873577-44874040 | Common:8; Rare:187 | ||||
| chr21:44939877-44940049 | Common:2; Rare:48 | ||||
| chr21:45287867-45288093 | Common:6; Rare:89 | ||||
| chr21:45455805-45456180 | Common:5; Rare:162; Clinvar:2; Clinvar (benign):2 | ||||
| chr21:45505601-45505883 | Common:3; Rare:116 | ||||
| chr21:45981519-45981841 | Common:23; Rare:79; Clinvar (benign):2 | ||||
| chr21:46001998-46002283 | Common:2; Rare:103; Clinvar:10; Clinvar (benign):10 |