| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43659458-43659603 | Common:1; Rare:47 | ||||
| chr21:43776241-43776599 | Common:5; Rare:125; Clinvar:2; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr21:43789363-43789632 | Common:1; Rare:98 | ||||
| chr21:44012261-44012541 | Common:1; Rare:100 | ||||
| chr21:44299792-44300105 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr21:44339209-44339539 | Common:3; Rare:89 | ||||
| chr21:44775156-44775187 | Rare:10 | ||||
| chr21:44801707-44801880 | Rare:68 | ||||
| chr21:44872668-44872758 | Common:2; Rare:24 | ||||
| chr21:44873503-44873579 | Rare:18 | ||||
| chr21:44873623-44874038 | Common:8; Rare:166 | ||||
| chr21:44939900-44940072 | Common:2; Rare:47 | ||||
| chr21:45073788-45073842 | Common:2; Rare:23 | ||||
| chr21:45180406-45180546 | Rare:30 | ||||
| chr21:45287797-45288129 | Common:6; Rare:131 |