Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:42496185-42496536 | Common:2; Rare:86 | ||||
chr21:42879567-42879669 | Common:2; Rare:26 | ||||
chr21:42893087-42893334 | Common:3; Rare:81 | ||||
chr21:43659467-43659638 | Common:1; Rare:55 | ||||
chr21:43728550-43728905 | Common:3; Rare:92 | ||||
chr21:43740800-43741010 | Common:3; Rare:71 | ||||
chr21:43776204-43776379 | Common:2; Rare:66; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr21:43789363-43789624 | Common:1; Rare:95 | ||||
chr21:44299981-44300117 | Rare:54; Clinvar (benign):1 | ||||
chr21:44339213-44339443 | Common:2; Rare:72 | ||||
chr21:44801774-44801876 | Rare:42 | ||||
chr21:44873506-44873590 | Rare:22 | ||||
chr21:44873606-44874040 | Common:8; Rare:175 | ||||
chr21:45073583-45073839 | Common:4; Rare:59 | ||||
chr21:45287867-45288093 | Common:6; Rare:89 |