| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873506-44873537 | Rare:12 | ||||
| chr21:44873600-44874103 | Common:9; Rare:192 | ||||
| chr21:44914229-44914469 | Common:2; Rare:50 | ||||
| chr21:44928653-44928752 | Common:1; Rare:19 | ||||
| chr21:44931935-44932014 | Rare:16 | ||||
| chr21:44939920-44940051 | Common:1; Rare:39 | ||||
| chr21:45287867-45288093 | Common:6; Rare:89 | ||||
| chr21:45455396-45455558 | Common:1; Rare:65 | ||||
| chr21:45455725-45455888 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr21:45492920-45493206 | Common:6; Rare:86 | ||||
| chr21:45542366-45542539 | Rare:62 | ||||
| chr21:45981505-45981824 | Common:23; Rare:75; Clinvar (benign):2 | ||||
| chr21:46184413-46184697 | Common:3; Rare:26 | ||||
| chr21:46286209-46286401 | Common:4; Rare:73 | ||||
| chr21:46286547-46286640 | Common:1; Rare:26 |