Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:55214826-55214903 | Common:1; Rare:27 | ||||
chr1:55215093-55215432 | Rare:116 | ||||
chr1:56513079-56513450 | Common:3; Rare:76 | ||||
chr1:56645055-56645377 | Common:1; Rare:107 | ||||
chr1:58546682-58546816 | Common:4; Rare:59 | ||||
chr1:58576899-58577633 | Common:2; Rare:203; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:58577673-58577996 | Common:3; Rare:38 | ||||
chr1:58668708-58668727 | Rare:6 | ||||
chr1:58689258-58689283 | Rare:5 | ||||
chr1:58689699-58689774 | Rare:16 | ||||
chr1:58689922-58690225 | Common:2; Rare:58 | ||||
chr1:58690388-58690676 | Common:2; Rare:58 | ||||
chr1:58699984-58700577 | Common:6; Rare:182 | ||||
chr1:58783893-58784394 | Common:1; Rare:134 | ||||
chr1:59296495-59296837 | Common:12; Rare:88 |