Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373302-234373776 | Common:1; Rare:212; Clinvar (benign):7 | ||||
chr1:235128779-235129105 | Common:1; Rare:127 | ||||
chr1:235328116-235328539 | Common:3; Rare:120 | ||||
chr1:235866838-235867177 | Common:3; Rare:104 | ||||
chr1:236604456-236604657 | Common:4; Rare:60 | ||||
chr1:236795157-236795457 | Common:4; Rare:128; Clinvar:4 | ||||
chr1:243255060-243255151 | Rare:24 | ||||
chr1:243255759-243256128 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244835152-244835338 | Rare:76 | ||||
chr1:244835584-244835730 | Common:1; Rare:65; Clinvar (benign):4 | ||||
chr1:244856455-244856792 | Common:1; Rare:75; Clinvar (benign):2 | ||||
chr1:244863616-244864110 | Common:1; Rare:162; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr1:244864384-244864669 | Rare:104 | ||||
chr1:244969537-244969801 | Rare:73 | ||||
chr1:246566167-246566640 | Common:3; Rare:151 |