| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39445751-39446088 | Common:4; Rare:97 | ||||
| chr21:39451661-39452139 | Common:3; Rare:136 | ||||
| chr21:39452549-39452776 | Common:1; Rare:38 | ||||
| chr21:41426058-41426257 | Common:3; Rare:44 | ||||
| chr21:42879538-42879669 | Common:3; Rare:40 | ||||
| chr21:42893064-42893372 | Common:4; Rare:110 | ||||
| chr21:42974352-42974649 | Common:1; Rare:111 | ||||
| chr21:43659480-43659585 | Common:1; Rare:33 | ||||
| chr21:43728604-43728878 | Common:3; Rare:68 | ||||
| chr21:43776229-43776485 | Common:5; Rare:94; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr21:43789371-43789617 | Common:1; Rare:89 | ||||
| chr21:44299782-44300096 | Common:2; Rare:109 | ||||
| chr21:44801752-44801880 | Rare:57 | ||||
| chr21:44873605-44874050 | Common:8; Rare:180 | ||||
| chr21:44939856-44940071 | Common:3; Rare:56 |