Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:218285095-218285350 | Common:4; Rare:104 | ||||
chr1:219173777-219173900 | Common:1; Rare:67 | ||||
chr1:220046421-220046533 | Common:1; Rare:45 | ||||
chr1:221742001-221742288 | Rare:73 | ||||
chr1:222589874-222589972 | Common:1; Rare:23 | ||||
chr1:222644159-222644387 | Common:1; Rare:65 | ||||
chr1:222712444-222712872 | Common:3; Rare:151 | ||||
chr1:222713243-222713416 | Common:1; Rare:53 | ||||
chr1:223701137-223701161 | Rare:7 | ||||
chr1:223701357-223701598 | Common:2; Rare:33 | ||||
chr1:223712368-223712636 | Common:2; Rare:91 | ||||
chr1:224114018-224114156 | Common:1; Rare:54 | ||||
chr1:224183001-224183361 | Common:3; Rare:139 | ||||
chr1:224330107-224330203 | Common:2; Rare:45 | ||||
chr1:225427998-225428286 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):2 |