Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:144645729-144646225 | Common:1; Rare:139 | ||||
chr4:144646343-144646723 | Common:1; Rare:86 | ||||
chr4:144647186-144647212 | Common:1; Rare:3 | ||||
chr4:145098141-145098371 | Rare:80 | ||||
chr4:145480567-145480777 | Common:1; Rare:41 | ||||
chr4:145481562-145481724 | Rare:41 | ||||
chr4:145482675-145482791 | Rare:35 | ||||
chr4:145482869-145483026 | Rare:30 | ||||
chr4:145619081-145619416 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
chr4:148442368-148442712 | Rare:100; Clinvar:4; Clinvar (benign):3 | ||||
chr4:151099444-151099713 | Common:3; Rare:103 | ||||
chr4:152536054-152536394 | Common:2; Rare:128 | ||||
chr4:152679889-152680120 | Rare:75 | ||||
chr4:152779642-152780016 | Common:2; Rare:98 | ||||
chr4:153466233-153466395 | Common:3; Rare:70 |