Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236142022-236142080 | Rare:20 | ||||
chr1:236142302-236142761 | Common:7; Rare:135 | ||||
chr1:236281365-236281674 | Common:2; Rare:77 | ||||
chr1:236281828-236282316 | Common:7; Rare:145 | ||||
chr1:236395112-236395504 | Rare:91 | ||||
chr1:236523791-236524041 | Common:4; Rare:65 | ||||
chr1:236524426-236524675 | Common:2; Rare:63 | ||||
chr1:236604417-236604869 | Common:5; Rare:129 | ||||
chr1:236686392-236686531 | Rare:58 | ||||
chr1:236794942-236795451 | Common:6; Rare:186; Clinvar:3 | ||||
chr1:236795459-236795959 | Common:6; Rare:196; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:239386502-239386597 | Rare:14 | ||||
chr1:239719790-239719848 | Rare:11 | ||||
chr1:241519066-241519319 | Common:1; Rare:47 | ||||
chr1:241519464-241519516 | Rare:17 |