| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39612802-39613016 | Rare:62 | ||||
| chr21:41767027-41767160 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:41879301-41879541 | Common:5; Rare:80 | ||||
| chr21:42514394-42514551 | Rare:33 | ||||
| chr21:42893050-42893353 | Common:4; Rare:103 | ||||
| chr21:42974254-42974652 | Common:1; Rare:146 | ||||
| chr21:43659461-43659592 | Common:1; Rare:44 | ||||
| chr21:43789369-43789632 | Common:1; Rare:96 | ||||
| chr21:44339226-44339466 | Common:2; Rare:72 | ||||
| chr21:44801766-44801876 | Rare:48 | ||||
| chr21:44873505-44873602 | Rare:28 | ||||
| chr21:44873605-44874050 | Common:8; Rare:180 | ||||
| chr21:45287867-45288102 | Common:6; Rare:92 | ||||
| chr21:45493085-45493225 | Rare:56 | ||||
| chr21:45981499-45981946 | Common:24; Rare:119; Clinvar:5; Clinvar (benign):4 |