Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:65481836-65482003 | Common:1; Rare:32 | ||||
chr5:65563116-65563406 | Common:3; Rare:115 | ||||
chr5:65624462-65624765 | Common:11; Rare:56 | ||||
chr5:65722066-65722379 | Common:4; Rare:102 | ||||
chr5:65925581-65926007 | Rare:157 | ||||
chr5:66144154-66144351 | Common:2; Rare:69 | ||||
chr5:68215539-68215866 | Common:4; Rare:102 | ||||
chr5:68288310-68288557 | Common:4; Rare:72 | ||||
chr5:68292248-68292458 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
chr5:69166927-69167160 | Common:1; Rare:53 | ||||
chr5:69189464-69189566 | Common:1; Rare:29 | ||||
chr5:69369473-69370093 | Common:3; Rare:209 | ||||
chr5:69560103-69560269 | Common:1; Rare:43 | ||||
chr5:71587188-71587435 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
chr5:72816496-72816735 | Common:4; Rare:92 |