| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:40146427-40147023 | Common:18; Rare:236 | ||||
| chr21:40149609-40149896 | Common:1; Rare:58 | ||||
| chr21:40316087-40316365 | Common:1; Rare:47 | ||||
| chr21:40318280-40318850 | Common:3; Rare:114 | ||||
| chr21:40319178-40319802 | Common:5; Rare:189 | ||||
| chr21:40320614-40321188 | Common:3; Rare:342 | ||||
| chr21:40321233-40321633 | Common:2; Rare:119 | ||||
| chr21:40324367-40324845 | Rare:246 | ||||
| chr21:40324775-40325464 | Common:6; Rare:312 | ||||
| chr21:40325463-40326185 | Rare:209 | ||||
| chr21:40326222-40326622 | Common:7; Rare:173 | ||||
| chr21:40333731-40334493 | Common:8; Rare:236 | ||||
| chr21:40335739-40336033 | Common:1; Rare:77 | ||||
| chr21:40337863-40339790 | Common:20; Rare:801; Clinvar (benign):2 | ||||
| chr21:40340263-40341107 | Common:7; Rare:295 |