| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44300388-44300633 | Rare:65 | ||||
| chr21:44339087-44339202 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:44339318-44339592 | Common:2; Rare:67 | ||||
| chr21:44353259-44353360 | Common:1; Rare:25 | ||||
| chr21:44353427-44353712 | Common:3; Rare:60 | ||||
| chr21:44353828-44354276 | Rare:94 | ||||
| chr21:44801718-44802003 | Common:1; Rare:101 | ||||
| chr21:44817652-44817967 | Common:17; Rare:116 | ||||
| chr21:44817996-44818327 | Rare:133 | ||||
| chr21:44872592-44872749 | Common:2; Rare:39 | ||||
| chr21:44873580-44874166 | Common:9; Rare:216 | ||||
| chr21:44874169-44874178 | Rare:3 | ||||
| chr21:44914292-44914414 | Common:1; Rare:22 | ||||
| chr21:44920816-44921134 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr21:44921347-44921481 | Common:1; Rare:31 |