| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44872309-44873256 | Common:21; Rare:391 | ||||
| chr21:44873270-44873550 | Common:2; Rare:79 | ||||
| chr21:44873570-44874260 | Common:59; Rare:1322 | ||||
| chr21:44874282-44874682 | Common:12; Rare:246 | ||||
| chr21:44939763-44940163 | Common:22; Rare:411 | ||||
| chr21:44940169-44940569 | Common:1; Rare:131 | ||||
| chr21:45073379-45073919 | Common:21; Rare:334 | ||||
| chr21:45073898-45074202 | Common:9; Rare:135 | ||||
| chr21:45074249-45074991 | Common:16; Rare:884 | ||||
| chr21:45074920-45075320 | Common:5; Rare:112 | ||||
| chr21:45287767-45288172 | Common:41; Rare:802 | ||||
| chr21:45404791-45405212 | Common:48; Rare:694 | ||||
| chr21:45405420-45405890 | Common:13; Rare:528 | ||||
| chr21:45541687-45542677 | Common:13; Rare:845 | ||||
| chr21:45981412-45981860 | Common:141; Rare:441; Clinvar:3; Clinvar (benign):10 |