| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:38498393-38498729 | Common:1; Rare:46 | ||||
| chr21:39380254-39380487 | Common:1; Rare:113 | ||||
| chr21:39445765-39445913 | Common:2; Rare:49 | ||||
| chr21:41316652-41316868 | Common:3; Rare:48 | ||||
| chr21:41361962-41362035 | Rare:11 | ||||
| chr21:41426149-41426254 | Common:1; Rare:18 | ||||
| chr21:41508152-41508272 | Common:1; Rare:22 | ||||
| chr21:41767046-41767160 | Common:3; Rare:53; Clinvar:1 | ||||
| chr21:42653475-42653793 | Common:5; Rare:50 | ||||
| chr21:42893064-42893347 | Common:4; Rare:97 | ||||
| chr21:43789377-43789617 | Common:1; Rare:87 | ||||
| chr21:44801728-44801876 | Rare:64 | ||||
| chr21:45287857-45288088 | Common:6; Rare:94 | ||||
| chr21:45981505-45981946 | Common:24; Rare:118; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45986518-45987004 | Common:6; Rare:163; Clinvar:22; Clinvar (benign):11 |