Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:183023760-183024163 | Common:1; Rare:130 | ||||
chr1:183185935-183186504 | Common:6; Rare:142; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:183186569-183186648 | Common:3; Rare:11 | ||||
chr1:183418332-183418434 | Rare:24 | ||||
chr1:183471620-183472168 | Common:2; Rare:109 | ||||
chr1:183472208-183472612 | Common:2; Rare:123 | ||||
chr1:183472745-183472971 | Common:3; Rare:54 | ||||
chr1:183472982-183473172 | Common:1; Rare:39 | ||||
chr1:183569298-183569448 | Common:1; Rare:20 | ||||
chr1:183590276-183590596 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:183633793-183634038 | Common:4; Rare:44 | ||||
chr1:183635155-183635304 | Rare:39 | ||||
chr1:183635363-183636115 | Common:8; Rare:219 | ||||
chr1:183636230-183636338 | Rare:19 | ||||
chr1:183805007-183805166 | Rare:39 |