Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:206507373-206507531 | Common:1; Rare:33 | ||||
chr1:206557031-206557335 | Common:1; Rare:61 | ||||
chr1:206557386-206557580 | Common:1; Rare:49 | ||||
chr1:206635379-206635592 | Common:2; Rare:68 | ||||
chr1:206635810-206635959 | Rare:41 | ||||
chr1:207050947-207051118 | Common:1; Rare:78 | ||||
chr1:207052955-207053353 | Common:1; Rare:103 | ||||
chr1:207321620-207321819 | Rare:47 | ||||
chr1:207751920-207752238 | Common:1; Rare:104; Clinvar:1 | ||||
chr1:208244255-208244568 | Common:1; Rare:90 | ||||
chr1:209675258-209675476 | Common:1; Rare:52 | ||||
chr1:209784521-209784766 | Common:1; Rare:80 | ||||
chr1:209806126-209806299 | Common:5; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827853-209828061 | Common:1; Rare:56 | ||||
chr1:210328832-210328953 | Common:1; Rare:41 |