| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42010302-42010376 | Rare:22 | ||||
| chr21:42496205-42496583 | Common:2; Rare:92 | ||||
| chr21:42514428-42514598 | Rare:32 | ||||
| chr21:42653531-42653771 | Common:3; Rare:43 | ||||
| chr21:42879025-42879125 | Common:1; Rare:28 | ||||
| chr21:42879554-42879669 | Common:2; Rare:29 | ||||
| chr21:42893050-42893354 | Common:4; Rare:104 | ||||
| chr21:43659461-43659592 | Common:1; Rare:44 | ||||
| chr21:43789363-43789631 | Common:1; Rare:98 | ||||
| chr21:44299957-44300112 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr21:44339184-44339469 | Common:2; Rare:93 | ||||
| chr21:44801739-44801876 | Rare:62 | ||||
| chr21:44873506-44874070 | Common:9; Rare:213 | ||||
| chr21:44939908-44940052 | Common:2; Rare:41 | ||||
| chr21:45287845-45288108 | Common:6; Rare:101 |