| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42973884-42974995 | Common:11; Rare:1261 | ||||
| chr21:42974910-42975768 | Common:44; Rare:897 | ||||
| chr21:43107059-43107635 | Common:21; Rare:367 | ||||
| chr21:43659300-43659738 | Common:9; Rare:473 | ||||
| chr21:43718881-43719212 | Common:23; Rare:340 | ||||
| chr21:43728083-43728483 | Common:2; Rare:85 | ||||
| chr21:43728491-43728970 | Common:18; Rare:611 | ||||
| chr21:43728872-43729272 | Common:6; Rare:99 | ||||
| chr21:43775832-43776900 | Common:42; Rare:1250; Clinvar:20; Clinvar (benign):68; Clinvar (pathogenic):4 | ||||
| chr21:43789264-43789664 | Common:7; Rare:741 | ||||
| chr21:43790168-43791292 | Common:7; Rare:349 | ||||
| chr21:43864308-43865516 | Common:13; Rare:1018 | ||||
| chr21:43866260-43866480 | Common:1; Rare:97 | ||||
| chr21:43866384-43867342 | Common:7; Rare:428 | ||||
| chr21:43916401-43916915 | Common:8; Rare:179 |