Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52141801-52142152 | Common:1; Rare:86 | ||||
chr1:52142670-52143130 | Rare:103 | ||||
chr1:52366135-52366322 | Common:1; Rare:55 | ||||
chr1:52404358-52404678 | Common:1; Rare:87 | ||||
chr1:52553032-52553431 | Common:4; Rare:111 | ||||
chr1:52553443-52553701 | Common:3; Rare:74 | ||||
chr1:52698302-52698513 | Common:3; Rare:70; Clinvar (pathogenic):1 | ||||
chr1:52927010-52927370 | Common:4; Rare:89 | ||||
chr1:52927497-52927897 | Common:6; Rare:104 | ||||
chr1:53014866-53015018 | Rare:44 | ||||
chr1:53062051-53062215 | Common:4; Rare:35 | ||||
chr1:53062559-53062959 | Common:9; Rare:88 | ||||
chr1:53196580-53196854 | Common:1; Rare:83; Clinvar:6; Clinvar (benign):1 | ||||
chr1:53220218-53220369 | Rare:76 | ||||
chr1:53220560-53220763 | Common:2; Rare:93 |