| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42893088-42893369 | Common:3; Rare:101 | ||||
| chr21:42974221-42974646 | Common:1; Rare:157 | ||||
| chr21:43659480-43659585 | Common:1; Rare:33 | ||||
| chr21:44299992-44300107 | Rare:48; Clinvar (benign):1 | ||||
| chr21:44339226-44339459 | Common:2; Rare:70 | ||||
| chr21:44873626-44874040 | Common:8; Rare:166 | ||||
| chr21:45287861-45288085 | Common:6; Rare:91 | ||||
| chr21:45981531-45981946 | Common:24; Rare:111; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45986576-45987004 | Common:6; Rare:147; Clinvar:21; Clinvar (benign):11 | ||||
| chr21:45987006-45987175 | Common:1; Rare:61; Clinvar:9; Clinvar (benign):4 | ||||
| chr21:45998948-45999217 | Common:2; Rare:89; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr21:46001988-46002393 | Common:2; Rare:139; Clinvar:18; Clinvar (benign):14 | ||||
| chr21:46184409-46184725 | Common:3; Rare:29 | ||||
| chr21:46286276-46286424 | Common:2; Rare:52 | ||||
| chr21:46323813-46324199 | Common:2; Rare:137; Clinvar:2; Clinvar (benign):1 |