| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36990187-36990446 | Common:5; Rare:83; Clinvar (benign):4 | ||||
| chr21:37267290-37267686 | Common:4; Rare:141 | ||||
| chr21:39451596-39451939 | Common:1; Rare:78 | ||||
| chr21:39612778-39612990 | Rare:66 | ||||
| chr21:41767060-41767167 | Common:3; Rare:49; Clinvar:1 | ||||
| chr21:42514694-42514895 | Common:1; Rare:36 | ||||
| chr21:42878964-42879189 | Common:2; Rare:67 | ||||
| chr21:42879554-42879665 | Common:2; Rare:28 | ||||
| chr21:42893016-42893347 | Common:5; Rare:116 | ||||
| chr21:42974237-42974594 | Common:1; Rare:138 | ||||
| chr21:43659461-43659667 | Common:1; Rare:67 | ||||
| chr21:44299984-44300131 | Rare:55; Clinvar (benign):1 | ||||
| chr21:44801752-44801860 | Rare:52 | ||||
| chr21:44873503-44873539 | Rare:12 | ||||
| chr21:44873540-44874005 | Common:8; Rare:182 |