Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45478634-45478784 | Common:4; Rare:50 | ||||
chr21:45992188-45992397 | Common:1; Rare:71; Clinvar:8; Clinvar (benign):3 | ||||
chr21:45998160-45998425 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr21:46125281-46125617 | Common:4; Rare:184; Clinvar:19; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
chr21:46125918-46126536 | Common:9; Rare:321; Clinvar:39; Clinvar (benign):27; Clinvar (pathogenic):4 | ||||
chr21:46131113-46131204 | Rare:36 | ||||
chr21:46131901-46132024 | Common:1; Rare:61; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
chr21:46636213-46636454 | Common:1; Rare:47 | ||||
chr22:11859731-11859866 | Rare:5 | ||||
chr22:16601129-16601488 | Common:2; Rare:142 | ||||
chr22:19171615-19171729 | Rare:37 | ||||
chr22:22298037-22298198 | Common:2; Rare:71 | ||||
chr22:22818934-22819088 | Rare:21 | ||||
chr22:22901005-22901099 | Rare:31 | ||||
chr22:23181715-23181824 | Common:1; Rare:46 |