| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:41508040-41508289 | Common:2; Rare:56 | ||||
| chr21:41767024-41767167 | Common:4; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:42315346-42315684 | Common:1; Rare:114 | ||||
| chr21:42513608-42513884 | Rare:81 | ||||
| chr21:42514428-42514560 | Rare:28 | ||||
| chr21:42731696-42731877 | Rare:61 | ||||
| chr21:42879532-42879680 | Common:3; Rare:44 | ||||
| chr21:42893064-42893342 | Common:4; Rare:93 | ||||
| chr21:43659467-43659603 | Common:1; Rare:45 | ||||
| chr21:43789375-43789608 | Common:1; Rare:82 | ||||
| chr21:44425567-44425699 | Common:1; Rare:51 | ||||
| chr21:44801774-44801880 | Rare:43 | ||||
| chr21:44873606-44874050 | Common:8; Rare:179 | ||||
| chr21:44939856-44940052 | Common:3; Rare:52 | ||||
| chr21:45287879-45288085 | Common:5; Rare:80 |