Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373311-234373776 | Common:1; Rare:210; Clinvar (benign):7 | ||||
chr1:235866869-235867198 | Common:3; Rare:106 | ||||
chr1:236523867-236524036 | Common:2; Rare:44 | ||||
chr1:236604476-236604659 | Common:4; Rare:52 | ||||
chr1:236795081-236795426 | Common:6; Rare:142; Clinvar:3 | ||||
chr1:241519655-241519936 | Common:2; Rare:97; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
chr1:241848123-241848255 | Common:1; Rare:23 | ||||
chr1:243255041-243255438 | Common:1; Rare:97 | ||||
chr1:243255763-243256118 | Rare:100; Clinvar:4 | ||||
chr1:244451840-244452097 | Rare:97 | ||||
chr1:246566185-246566563 | Common:1; Rare:122 | ||||
chr1:246724256-246724432 | Common:2; Rare:70 | ||||
chr1:248906100-248906288 | Rare:78 | ||||
chr10:988298-988482 | Common:1; Rare:73 | ||||
chr10:1048872-1049099 | Common:2; Rare:115 |