| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43728748-43729186 | Common:4; Rare:119 | ||||
| chr21:43745193-43745481 | Common:2; Rare:57 | ||||
| chr21:43776228-43776643 | Common:5; Rare:145; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr21:43789369-43789718 | Common:2; Rare:124 | ||||
| chr21:44012244-44012544 | Common:1; Rare:106 | ||||
| chr21:44339203-44339463 | Common:2; Rare:80 | ||||
| chr21:44455286-44455540 | Common:3; Rare:58 | ||||
| chr21:44801703-44801905 | Rare:78 | ||||
| chr21:44873503-44873900 | Common:4; Rare:153 | ||||
| chr21:44939871-44940211 | Common:3; Rare:98 | ||||
| chr21:45073789-45073845 | Common:2; Rare:26 | ||||
| chr21:45074479-45074588 | Common:2; Rare:50 | ||||
| chr21:45287816-45288092 | Common:6; Rare:111 | ||||
| chr21:45404874-45405233 | Common:13; Rare:197 | ||||
| chr21:45542363-45542503 | Rare:50 |